부산대학교 도서관

Elhussein A.E. Elhassan; Tereza Kmochová; Katherine A. Benson; Neil K. Fennelly; Veronika Barešová; Kendrah Kidd; Brendan Doyle; Anthony Dorman; Martina M. Morrin; Niamh C. Kyne; Petr Vyleťal; Hana Hartmannová; Kateřina Hodaňová; Jana Sovová; Dita Mušálková; Alena Vrbacká; Anna Přistoupilová; Jan Živný; Klára Svojšová; Martin Radina; Viktor Stránecký; Dmitry Loginov; Petr Pompach; Petr Novák; Zdislava Vaníčková; Hana Hansíková; Silvie Rajnochová-Bloudíčková; Ondřej Viklický; Helena Hůlková; Gianpiero L. Cavalleri; Aleš Hnízda; Anthony J. Bleyer; Stanislav Kmoch; Peter J. Conlon; Martina Živná

Kidney International Reports, Vol 9, Iss 7, Pp 2209-2226 (2024)

Mušálková D; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Radina M; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Kidd K; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.; Hartmannová H; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Trešlová H; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Hodaňová K; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Vyleťal P; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Vrbacká A; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Votruba M; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Sanchez A; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.; Martin L; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.; Taylor A; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.; Kim A; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.; Rudl Kulhavá L; Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.; Hricko J; Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.; Čajka T; Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.; Živná M; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.; Bleyer AJ; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.; Kmoch S; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.

Publisher: Wolters Kluwer Health, Inc. on behalf of the American Society of Nephrology Country of Publication: United States NLM ID: 101766381 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2641-7650 (Electronic) Linking ISSN: 26417650 NLM ISO Abbreviation: Kidney360 Subsets: MEDLINE; In Process

Vrbacká A; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Přistoupilová A; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Kidd KO; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Wake Forest University School of Medicine, Section on Nephrology, Winston-Salem, North Carolina, USA.; Janoušek V; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Radina M; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Vyleťal P; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Bitar I; Department of Microbiology, Faculty of Medicine and University Hospital Pilsen, Charles University, Pilsen, Czechia.; Biomedical Center, Faculty of Medicine, Charles University, Pilsen, Czechia.; Stránecký V; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Steiner-Mrázová L; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Trešlová H; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Sovová J; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Hodaňová K; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Hartmannová H; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Mušálková D; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Svojšová K; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Kmochová T; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Barešová V; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Taylor A; Wake Forest University School of Medicine, Section on Nephrology, Winston-Salem, North Carolina, USA.; Martin L; Wake Forest University School of Medicine, Section on Nephrology, Winston-Salem, North Carolina, USA.; Sanchez A; Wake Forest University School of Medicine, Section on Nephrology, Winston-Salem, North Carolina, USA.; Ryšavá R; Department of Nephrology, First Faculty of Medicine, Charles University in Prague and General Teaching Hospital in Prague, Prague, Czech Republic.; Lajtmanová I; B. Braun Avitum, Bratislava, Slovakia.; Rajnochová-Bloudíčková S; Department of Nephrology, Transplant Centre, Institute for Clinical and Experimental Medicine, Videnska 1958, Prague 14021, Czech Republic.; Viklický O; Department of Nephrology, Transplant Centre, Institute for Clinical and Experimental Medicine, Videnska 1958, Prague 14021, Czech Republic.; Papagregorius G; Molecular Medicine Research Center, biobank.cy Center of Excellence in Biobanking and Biomedical Research, University of Cyprus, Nicosia, Cyprus.; Deltas C; Molecular Medicine Research Center, biobank.cy Center of Excellence in Biobanking and Biomedical Research, University of Cyprus, Nicosia, Cyprus.; Medical School, University of Cyprus, Nicosia, Cyprus.; Stavrou C; Evangelismos Private Hospital, Pafos, Cyprus.; Jorge S; Department of Nephrology and Renal Transplant, Hospital de Santa Maria, CHULN, EPE, Lisbon, Portugal.; Lopes JA; Department of Nephrology and Renal Transplant, Hospital de Santa Maria, CHULN, EPE, Lisbon, Portugal.; Rodrigues M; Department of Medical Genetics, Hospital de Santa Maria, ULSSM, Lisbon, Portugal.; Elhassan E; Department of Nephrology Beaumont Hospital Dublin Ireland.; Clince M; Department of Nephrology Beaumont Hospital Dublin Ireland.; Rowan C; Department of Nephrology Beaumont Hospital Dublin Ireland.; Conlon P; Department of Nephrology and Renal Transplant, Hospital de Santa Maria, CHULN, EPE, Lisbon, Portugal.; Department of Medicine, Royal College of Surgeons, Dublin, Ireland.; Teltsh O; School of Pharmacy and Biomolecular Sciences, Royal College of Surgeons, Dublin, Ireland.; Cavalleri GL; Department of Nephrology and Renal Transplant, Hospital de Santa Maria, CHULN, EPE, Lisbon, Portugal.; Blumenstiel B; Broad Clinical Labs, The Broad Institute, Cambridge, Massachusetts, USA.; Toledo D; Broad Clinical Labs, The Broad Institute, Cambridge, Massachusetts, USA.; DiStefano M; Broad Clinical Labs, The Broad Institute, Cambridge, Massachusetts, USA.; DeFelice M; Broad Clinical Labs, The Broad Institute, Cambridge, Massachusetts, USA.; Živná M; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Wake Forest University School of Medicine, Section on Nephrology, Winston-Salem, North Carolina, USA.; Bleyer AJ Sr; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Wake Forest University School of Medicine, Section on Nephrology, Winston-Salem, North Carolina, USA.; Kmoch S; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Wake Forest University School of Medicine, Section on Nephrology, Winston-Salem, North Carolina, USA.

Country of Publication: United States NLM ID: 101680187 Publication Model: Electronic Cited Medium: Internet ISSN: 2692-8205 (Electronic) Linking ISSN: 26928205 NLM ISO Abbreviation: bioRxiv Subsets: PubMed not MEDLINE

Živná M; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina.; Dostálová G; Second Department of Internal Cardiovascular Medicine, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.; Barešová V; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Mušálková D; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Svojšová K; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Meiseles D; The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.; Kinstlinger S; The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.; Kuchař L; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Asfaw B; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Poupětová H; Department of Neurology and Centre of Clinical Neuroscience, First Faculty of Medicine, Charles University and General University Hospital in Prague, Czech Republic.; Vlášková H; Diagnostic Laboratory, Department of Pediatrics and Inherited Metabolic Disorders, General University Hospital, Prague, Czech Republic.; Kmochová T; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Vyleťal P; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Hartmannová H; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Hodaňová K; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Stránecký V; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Steiner-Mrázová L; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Hnízda A; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Živný J; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Radina M; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Votruba M; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Sovová J; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Trešlová H; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Stolnaja L; Diagnostic Laboratory, Department of Pediatrics and Inherited Metabolic Disorders, General University Hospital, Prague, Czech Republic.; Reková P; Department of Neurology and Centre of Clinical Neuroscience, First Faculty of Medicine, Charles University and General University Hospital in Prague, Czech Republic.; Roblová L; Second Department of Internal Cardiovascular Medicine, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.; Honsová E; AeskuLab Pathology, Prague, Czech Republic.; Institute of Pathology, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.; Rychlík I; Department of Medicine, Third Faculty of Medicine, Charles University in Prague and Faculty Hospital Kralovske Vinohrady, Prague, Czech Republic.; Dvela-Levitt M; The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.; Bleyer AJ; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina.; Linhart A; Second Department of Internal Cardiovascular Medicine, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.; Sikora J; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Institute of Pathology, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.; Kmoch S; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital, Prague, Czech Republic.; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina.

Publisher: Wolters Kluwer Health, on behalf of the American Society of Nephrology Country of Publication: United States NLM ID: 9013836 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1533-3450 (Electronic) Linking ISSN: 10466673 NLM ISO Abbreviation: J Am Soc Nephrol Subsets: MEDLINE; In Process

Zivna, M.; Dostalova, G.; Baresova, V.; Musalkova, D.; Kuchar, L.; Asfaw, B.; Poupetova, H.; Vlaskova, H.; Kmochova, T.; Vyletal, P.; Hartmannova, H.; Hodanova, K.; Steiner-Mrazova, L.; Hnizda, A.; Suneghova, K.; Treslova, H.; Rekova, P.; Roblova, L.; Honsova, E.; Hulkova, H.; Rychlik, I.; Bleyer, A.; Linhart, A.; Sikora, J.; Kmoch, S.

MOLECULAR BIOLOGY OF THE CELL; JAN 1 2024, 35 1, 25p.

Mušálková D; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic.; Přistoupilová A; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic.; Jedličková I; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic.; Hartmannová H; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic.; Trešlová H; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic.; Nosková L; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic.; Hodaňová K; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic.; Bittmanová P; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic.; Stránecký V; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic.; Jiřička V; Department of Psychology, Prison Service of the Czech Republic, Prague, Czech Republic.; Department of Psychiatry, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.; Langmajerová M; Department of Psychiatry, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.; Woodbury-Smith M; The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Faculty of Medical Sciences, Biosciences Institute, Newcastle University, Newcastle upon Tyne, UK.; Zarrei M; The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Trost B; The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Scherer SW; The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Molecular Genetics and McLaughlin Centre, University of Toronto, Toronto, Ontario, Canada.; Bleyer AJ; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic.; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Vevera J; Department of Psychiatry, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.; Department of Psychiatry, University Hospital Pilsen, Pilsen, Czech Republic.; Kmoch S; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic.; Department of Psychiatry, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.

Publisher: Munksgaard Country of Publication: England NLM ID: 101129617 Publication Model: Print Cited Medium: Internet ISSN: 1601-183X (Electronic) Linking ISSN: 1601183X NLM ISO Abbreviation: Genes Brain Behav Subsets: MEDLINE

Bleyer, A. J.; Kmoch, S.; Antignac, C.; Robins, V.; Kidd, K.; Kelsoe, J. R.; Hladik, G.; Klemmer, P.; Knohl, S. J.; Scheinman, S. J.; Vo, N.; Santi, A.; Harris, A.; Canaday, O.; Weller, N.; Hulick, P. J.; Vogel, K.; Rahbari-Oskoui, F. F.; Tuazon, J.; Constantinou-Deltas, Constantinos D.; Somers, D.; Megarbane, A.; Kimmel, P. L.; Sperati, C. J.; Orr-Urtreger, A.; Ben-Shachar, S.; Waugh, D. A.; Mcginn, S.; Bleyer Jr., A. J.; Hodaňová, K.; Vyletal, P.; Živná, M.; Hart, T. C.; Hart, P. S.

Clinical Journal of the American Society of Nephrology
Clin.J.Am.Soc.Nephrol.

Vylet'al, P.; Kublová, M.; Kalbáčová, M.; Hodaňová, K.; Barešová, V.; Stibůrková, B.; Sikora, J.; Hůlková, H.; živný, J.; Majewski, J.; Simmonds, A.; Fryns, J.-P.; Venkat-Raman, G.; Elleder, M.; Kmoch, S.

Kidney International. 70:1155-1169

Kmochová T; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Kidd KO; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.; Orr A; Department of Ophthalmology and Visual Sciences, Dalhousie University, Halifax, Nova Scotia, Canada; Department of Pathology, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.; Hnízda A; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Hartmannová H; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Hodaňová K; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Vyleťal P; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Naušová K; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Brinsa V; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Trešlová H; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Sovová J; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Barešová V; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Svojšová K; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Vrbacká A; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Stránecký V; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Robins VC; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.; Taylor A; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.; Martin L; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.; Rivas-Chavez A; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.; Payne R; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.; Bleyer HA; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.; Williams A; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.; Rennke HG; Pathology Department, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.; Weins A; Pathology Department, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.; Short PJ; Sano Genetics Limited, London, UK.; Agrawal V; Division of Nephrology and Hypertension, Larner College of Medicine, University of Vermont, Burlington, Vermont, USA.; Storsley LJ; Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.; Waikar SS; Section of Nephrology, Boston University Chobanian and Avedisian School of Medicine, Boston, Massachusetts, USA.; McPhail ED; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.; Dasari S; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA.; Leung N; Division of Nephrology and Hypertension, Division of Hematology, Mayo Clinic, Rochester, Minnesota, USA.; Hewlett T; Division of Nephrology, Department of Medicine, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.; Yorke J; Department of Pathology, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.; Gaston D; Department of Pathology, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.; Geldenhuys L; Department of Pathology, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.; Samuels M; Department of Medicine Université de Montréal, Montreal, Quebec, Canada; Department of Biochemistry, Université de Montréal, Montreal, Quebec, Canada; Centre de Recherche du CHU Ste-Justine, Montreal, Quebec, Canada.; Levine AP; Research Department of Pathology, University College London, London, UK.; West M; Division of Nephrology, Department of Medicine, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.; Hůlková H; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic; Institute of Pathology, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Pompach P; Institute of Microbiology of the Czech Academy of Sciences, Vestec, Czech Republic.; Novák P; Institute of Microbiology of the Czech Academy of Sciences, Vestec, Czech Republic.; Weinberg RB; Section on Gastroenterology, Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA; Department of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.; Bedard K; Department of Pathology and Laboratory Medicine, Izaak Walton Killam Hospital, Halifax Nova Scotia, Canada.; Živná M; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.; Sikora J; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic; Institute of Pathology, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Bleyer AJ Sr; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA. Electronic address: ableyer@wakehealth.edu.; Kmoch S; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic; Section on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.

Publisher: Elsevier Country of Publication: United States NLM ID: 0323470 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1523-1755 (Electronic) Linking ISSN: 00852538 NLM ISO Abbreviation: Kidney Int Subsets: MEDLINE

Kidd, K.O.; Taylor, A.; Martin, L.; Robins, V.; Zivna, M.; Kmoch, S.; Bleyer, A.J.; Vrbacká, A.; Piherová, L.; Radina, M.; Vylet’al, P.; Hodanova, K.; Williams, A.H.; Sayer, J.A.; Mabillard, H.R.; Olinger, E.; Papagregoriou, G.; Deltas, C.; Stavrou, C.; Conlon, P.J.; Hogan, R.E.; Elhassan, E.A.E.; Springer, D.; Zima, T.; Izzi, C.; Pohludka, M.

In: BMC Nephrology. (BMC Nephrology, December 2024, 25(1))

Kubanek, M.; Binova, J.; Krebsova, A.; Kotrc, M.; Melenovsky, V.; Kautzner, J.; Piherova, L.; Hartmannova, H.; Hodanova, K.; Musalkova, D.; Stranecky, V.; Kmoch, S.; Palecek, T.; Chaloupka, A.; Grochova, I.; Krejci, J.; Petrkova, J.

In: ESC Heart Failure. (ESC Heart Failure, December 2024, 11(6):4127-4138)

Vylet'al P; Department of Paediatrics and Inherited Metabolic Disorders, Research Unit of Rare Diseases, First Faculty of Medicine, Charles University, Prague, Czechia.; Kidd K; Department of Paediatrics and Inherited Metabolic Disorders, Research Unit of Rare Diseases, First Faculty of Medicine, Charles University, Prague, Czechia.; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Ainsworth HC; Division of Public Health Sciences, Department of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Springer D; Institute of Medical Biochemistry and Laboratory Diagnostics, General University Hospital and the First Faculty of Medicine of Charles University, Prague, Czechia.; Vrbacká A; Department of Paediatrics and Inherited Metabolic Disorders, Research Unit of Rare Diseases, First Faculty of Medicine, Charles University, Prague, Czechia.; Přistoupilová A; Department of Paediatrics and Inherited Metabolic Disorders, Research Unit of Rare Diseases, First Faculty of Medicine, Charles University, Prague, Czechia.; Hughey RP; Renal-Electrolyte Division, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.; Alper SL; The Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.; Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts, USA.; Lennon N; The Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.; Harrison S; The Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.; Harden M; The Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.; Robins V; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Taylor A; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Martin L; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Howard K; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Bitar I; Biomedical Center and Institute of Microbiology, Faculty of Medicine in Pilsen of Charles University, Pilsen, Czechia.; Langefeld CD; Division of Public Health Sciences, Department of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Barešová V; Department of Paediatrics and Inherited Metabolic Disorders, Research Unit of Rare Diseases, First Faculty of Medicine, Charles University, Prague, Czechia.; Hartmannová H; Department of Paediatrics and Inherited Metabolic Disorders, Research Unit of Rare Diseases, First Faculty of Medicine, Charles University, Prague, Czechia.; Hodaňová K; Department of Paediatrics and Inherited Metabolic Disorders, Research Unit of Rare Diseases, First Faculty of Medicine, Charles University, Prague, Czechia.; Zima T; Institute of Medical Biochemistry and Laboratory Diagnostics, General University Hospital and the First Faculty of Medicine of Charles University, Prague, Czechia.; Živná M; Department of Paediatrics and Inherited Metabolic Disorders, Research Unit of Rare Diseases, First Faculty of Medicine, Charles University, Prague, Czechia.; Kmoch S; Department of Paediatrics and Inherited Metabolic Disorders, Research Unit of Rare Diseases, First Faculty of Medicine, Charles University, Prague, Czechia.; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Bleyer AJ; Department of Paediatrics and Inherited Metabolic Disorders, Research Unit of Rare Diseases, First Faculty of Medicine, Charles University, Prague, Czechia.; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.

Publisher: Karger Country of Publication: Switzerland NLM ID: 8109361 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1421-9670 (Electronic) Linking ISSN: 02508095 NLM ISO Abbreviation: Am J Nephrol Subsets: MEDLINE

Sicking M; Department of Medical Biochemistry and Molecular Biology, Saarland University, Homburg, Germany.; Živná M; Research Unit for Rare Diseases, Department of Pediatrics and Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Bhadra P; Center for Bioinformatics, Saarland University, Saarbrücken, Germany.; Barešová V; Research Unit for Rare Diseases, Department of Pediatrics and Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Tirincsi A; Department of Medical Biochemistry and Molecular Biology, Saarland University, Homburg, Germany.; Hadzibeganovic D; Department of Medical Biochemistry and Molecular Biology, Saarland University, Homburg, Germany.; Hodaňová K; Research Unit for Rare Diseases, Department of Pediatrics and Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Vyleťal P; Research Unit for Rare Diseases, Department of Pediatrics and Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Sovová J; Research Unit for Rare Diseases, Department of Pediatrics and Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Jedličková I; Research Unit for Rare Diseases, Department of Pediatrics and Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Jung M; Department of Medical Biochemistry and Molecular Biology, Saarland University, Homburg, Germany.; Bell T; Department of Chemistry, University of Nevada, Reno, NV, USA.; Helms V; Center for Bioinformatics, Saarland University, Saarbrücken, Germany.; Bleyer AJ; Research Unit for Rare Diseases, Department of Pediatrics and Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, NC, USA.; Kmoch S; Research Unit for Rare Diseases, Department of Pediatrics and Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Cavalié A; Experimental and Clinical Pharmacology and Toxicology, Pre-clinical Center for Molecular Signaling (PZMS), Saarland University, Homburg, Germany.; Lang S; Department of Medical Biochemistry and Molecular Biology, Saarland University, Homburg, Germany sven.lang@uni-saarland.de.

Publisher: Life Science Alliance, LLC Country of Publication: United States NLM ID: 101728869 Publication Model: Electronic-Print Cited Medium: Internet ISSN: 2575-1077 (Electronic) Linking ISSN: 25751077 NLM ISO Abbreviation: Life Sci Alliance Subsets: MEDLINE

SANTOS, A. ; Brás, A.C. ; Curto, A. ; Ramos, M. ; Kmochova, T. ; Hodanova, K. ; Zivna, M. ; Bleyer, A. ; Kmoch, S. ; Soto, K.

In Kidney International Reports March 2023 8(3) Supplement:S122-S122

Klem, K. ; Oravec, M. ; Holub, P. ; Šimor, J. ; Findurová, H. ; Surá, K. ; Veselá, B. ; Hodaňová, P. ; Jansen, M.A.K. ; Urban, O.

In Plant Physiology and Biochemistry 1 February 2022 172:111-124

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In Leukemia Research May 2023 128 Supplement

Hřebíček, M.; Hodaňová, K.; Ledvinová, J.; Sokolová, J.; Elleder, M.; Zeman, J.; Vepřeková, L.; Musilová, J.; Aerts, J. M. F. G.; Renkema, G. H.; Hřebíček, D.

Virchows Archiv: Official Journal of the European Society of Pathology. November 1996 429(4-5):305-309

Vevera J; Department of Psychiatry, Faculty of Medicine and University Hospital in Pilsen, Charles University, Prague, Czech Republic.; Department of Psychiatry, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.; Institute for Postgraduate Medical Education, Prague, Czech Republic.; Psychology Department, National Institute of Mental Health, Klecany, Czech Republic.; Zarrei M; The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Hartmannová H; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Jedličková I; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Mušálková D; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Přistoupilová A; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Oliveriusová P; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Trešlová H; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Nosková L; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Hodaňová K; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Stránecký V; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Jiřička V; Prison Service of the Czech Republic, Directorate General, Department of Psychology, Prague, Czech Republic.; Preiss M; Psychology Department, National Institute of Mental Health, Klecany, Czech Republic.; Psychology Department, University of New York in Prague, Prague, Czech Republic.; Příhodová K; Psychology Department, National Institute of Mental Health, Klecany, Czech Republic.; Šaligová J; Children's Faculty Hospital, Department of Pediatrics and Adolescent Medicine, Kosice, Slovakia.; Department of Pediatrics and Adolescent Medicine, Faculty of Medicine of Pavel Jozef Šafárik University Kosice, Kosice, Slovakia.; Wei J; The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Woodbury-Smith M; The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Institute of Neuroscience, Newcastle University, Sir James Spence Institute, Royal Victoria Infirmary, Newcastle upon Tyne, UK.; Bleyer AJ; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Section on Nephrology, Wake Forest School of Medicine, Medical Center Blvd., Winston-Salem, North Carolina, USA.; Scherer SW; The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Molecular Genetics and McLaughlin Centre, University of Toronto, Toronto, Ontario, Canada.; Kmoch S; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.

Publisher: Munksgaard Country of Publication: England NLM ID: 101129617 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1601-183X (Electronic) Linking ISSN: 1601183X NLM ISO Abbreviation: Genes Brain Behav Subsets: MEDLINE

Jorge S; Department of Nephrology and Renal Transplant, Hospital de Santa Maria, CHULN, EPE, Lisbon, Portugal.; Kidd K; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Czech Republic.; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Vylet'al P; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Czech Republic.; Nogueira E; Department of Nephrology and Renal Transplant, Hospital de Santa Maria, CHULN, EPE, Lisbon, Portugal.; Martin L; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Howard K; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Barešová V; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Czech Republic.; Hodaňová K; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Czech Republic.; Hnízda A; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Czech Republic.; Moldovan O; Genetic Department of Hospital de Santa Maria, CHULN, EPE, Lisbon, Portugal.; Silveira C; GenoMed - Diagnósticos de Medicina Molecular, S.A., Lisbon, Portugal.; Coutinho AM; GenoMed - Diagnósticos de Medicina Molecular, S.A., Lisbon, Portugal.; Lopes JA; Department of Nephrology and Renal Transplant, Hospital de Santa Maria, CHULN, EPE, Lisbon, Portugal.; Bleyer AJ; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Czech Republic.; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Kmoch S; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Czech Republic.; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Živná M; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Czech Republic.

Publisher: Elsevier Country of Publication: United States NLM ID: 101684752 Publication Model: eCollection Cited Medium: Internet ISSN: 2468-0249 (Electronic) Linking ISSN: 24680249 NLM ISO Abbreviation: Kidney Int Rep Subsets: PubMed not MEDLINE

Buglioni A; Division of Anatomic Pathology, Mayo Clinic, Rochester, Minnesota, USA.; Hasadsri L; Division of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.; Nasr SH; Division of Anatomic Pathology, Mayo Clinic, Rochester, Minnesota, USA.; Hogan MC; Division of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.; Moyer AM; Division of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.; Siddique K; Division of Pediatric Nephrology and Hypertension, DHR Health, Edinburg, Texas, USA.; Kidd K; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Research Unit of Rare Diseases, Department of Pediatric and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Kmoch S; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Research Unit of Rare Diseases, Department of Pediatric and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Hodaňová K; Research Unit of Rare Diseases, Department of Pediatric and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Bleyer AJ; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.; Research Unit of Rare Diseases, Department of Pediatric and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.; Alexander MP; Division of Anatomic Pathology, Mayo Clinic, Rochester, Minnesota, USA.

Publisher: Elsevier Country of Publication: United States NLM ID: 101684752 Publication Model: eCollection Cited Medium: Internet ISSN: 2468-0249 (Electronic) Linking ISSN: 24680249 NLM ISO Abbreviation: Kidney Int Rep Subsets: PubMed not MEDLINE