학술논문


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'학술논문' 에서 검색결과 2,023건 | 목록 1~20
Academic Journal
Bedin M; Laboratory of Epithelial Biology and Disease and.; Boyer O; Laboratory of Hereditary Kidney Disease, Imagine Institute, INSERM U1163, Université de Paris, Paris, France.; Department of Pediatric Nephrology and.; Servais A; Laboratory of Hereditary Kidney Disease, Imagine Institute, INSERM U1163, Université de Paris, Paris, France.; Department of Nephrology, Necker Hospital, Assistance Publique Hôpitaux de Paris (APHP), Paris, France.; Li Y; Institute of Genetic Epidemiology, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany.; Villoing-Gaudé L; Laboratory of Epithelial Biology and Disease and.; Tête MJ; Laboratory of Hereditary Kidney Disease, Imagine Institute, INSERM U1163, Université de Paris, Paris, France.; Cambier A; Department of Pediatric Nephrology and Transplantation, Robert-Debré Hospital, APHP, Paris, France.; Hogan J; Department of Pediatric Nephrology and Transplantation, Robert-Debré Hospital, APHP, Paris, France.; Baudouin V; Department of Pediatric Nephrology and Transplantation, Robert-Debré Hospital, APHP, Paris, France.; Krid S; Department of Pediatric Nephrology and.; Bensman A; Department of Pediatric Nephrology and.; Lammens F; Centre Hospitalier Régional Universitaire de Lille, Lille, France.; Louillet F; Centre Hospitalier Universitaire de Rouen, Rouen, France.; Ranchin B; Department of Pediatric Nephrology, Hospices Civils de Lyon, Bron, France.; Vigneau C; Centre Hospitalier Universitaire de Rennes, INSERM U1085 IRSET-9, Rennes, France.; Bouteau I; Centre Hospitalier Universitaire de Poitiers, Poitiers, France.; Isnard-Bagnis C; Department of Nephrology, Pitié Salpetrière Hospital, Paris, France.; Mache CJ; Children's Hospital, Medical University Graz, Graz, Austria.; Schäfer T; Renal Division, University Medical Center Freiburg, Freiburg, Germany.; Pape L; Department of Pediatric Kidney, Liver and Metabolic Disease, Hannover Medical School, Hannover, Germany.; Gödel M; Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Huber TB; Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Benz M; Kindernephrologie Dachau, Dachau, Germany.; Klaus G; Department of Child and Adolescent Medicine, University Medical Center Marburg-Giessen, Marburg, Germany.; Hansen M; KfH-Nierenzentrum für Kinder und Jugendliche und Clementine-Kinderhospital, Frankfurt, Germany.; Latta K; KfH-Nierenzentrum für Kinder und Jugendliche und Clementine-Kinderhospital, Frankfurt, Germany.; Gribouval O; Laboratory of Hereditary Kidney Disease, Imagine Institute, INSERM U1163, Université de Paris, Paris, France.; Morinière V; Department of Genetics, Necker Hospital, APHP, Paris, France.; Tournant C; Department of Genetics, Necker Hospital, APHP, Paris, France.; Grohmann M; Center for Human Genetics, Bioscientia, Ingelheim, Germany.; Center for Human Genetics, Mainz, Germany.; Kuhn E; Center for Human Genetics, Bioscientia, Ingelheim, Germany.; Wagner T; Center for Human Genetics, Bioscientia, Ingelheim, Germany.; Bole-Feysot C; Bioinformatic Platform, INSERM UMR 1163, Institut Imagine, Paris, France.; Bioinformatics Core Facility, Structure Fédérative de Recherche Necker, INSERM US24/CNRS UMS3633, Université de Paris, Paris, France.; Jabot-Hanin F; Bioinformatic Platform, INSERM UMR 1163, Institut Imagine, Paris, France.; Bioinformatics Core Facility, Structure Fédérative de Recherche Necker, INSERM US24/CNRS UMS3633, Université de Paris, Paris, France.; Nitschké P; Bioinformatic Platform, INSERM UMR 1163, Institut Imagine, Paris, France.; Bioinformatics Core Facility, Structure Fédérative de Recherche Necker, INSERM US24/CNRS UMS3633, Université de Paris, Paris, France.; Ahluwalia TS; Steno Diabetes Center Copenhagen, Gentofte, Denmark.; Köttgen A; Institute of Genetic Epidemiology, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany.; Andersen CBF; Department of Biomedicine, Aarhus University, Aarhus, Denmark.; Bergmann C; Center for Human Genetics, Bioscientia, Ingelheim, Germany.; Center for Human Genetics, Mainz, Germany.; Renal Division, Department of Medicine, University Hospital Freiburg, Freiburg, Germany.; Antignac C; Laboratory of Hereditary Kidney Disease, Imagine Institute, INSERM U1163, Université de Paris, Paris, France.; Department of Genetics, Necker Hospital, APHP, Paris, France.; Simons M; Laboratory of Epithelial Biology and Disease and.
Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 7802877 Publication Model: Print Cited Medium: Internet ISSN: 1558-8238 (Electronic) Linking ISSN: 00219738 NLM ISO Abbreviation: J Clin Invest Subsets: MEDLINE
Academic Journal
Ilias I. SiemposAndre C. KalilDrifa BelhadiViviane Cordeiro VeigaAlexandre Biasi CavalcantiWestyn Branch-EllimanEleni PapoutsiKonstantinos GkirgkirisNikoleta A. 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WestBabafemi TaiwoKaren KruegerJohnny PerezTriniece PearsonCatharine I. PaulesKathleen G. JulianDanish AhmadAlexander G. HajduczokHenry ArguinchonaChrista ArguinchonaNathaniel ErdmannPaul GoepfertNeera AhujaMaria G. FrankDavid WylesHeather YoungMyoung-don OhWan Beom ParkChang Kyung KangVincent MarconiAbeer MoannaSushma CribbsTelisha HarrisonEu Suk KimJongtak JungKyoung-Ho SongHong Bin KimSeow Yen TanHumaira ShafiMF Jaime ChienRaymond KC. FongDaniel D. MurrayJens LundgrenHenrik NielsenTomas JensenBarry S. ZingmanRobert GrossbergPaul F. RiskaOtto O. YangJenny AhnRubi AriasRekha R. RapakaNaomi HauserJames D. CampbellWilliam R. ShortPablo TebasJillian T. BaronSusan L.F. McLellanLucas S. BlantonJustin B. SeashoreC. Buddy CreechTodd W. RiceShannon WalkerIsaac P. ThomsenDiego Lopez de CastillaJason W. Van WinkleFrancis X. RiedoSurinder Kaur PadaAlvin DY. WangLi LinMichelle HarkinsGregory MertzNestor SosaLouis Yi Ann ChaiPaul Anantharajah TambyahSai Meng ThamSophia ArchuletaGabriel YanDavid A. LindholmAna Elizabeth MarkelzKatrin MendeRichard MularskiElizabeth HohmannMariam Torres-SotoNikolaus JilgRyan C. MavesGregory C. UtzSarah L. GeorgeDaniel F. HoftJames D. BrienRoger ParedesLourdes MateuCora LostePrincy KumarSarah ThorntonSharmila MohanrajNoreen A. HynesLauren M. SauerChristopher J. ColomboChristina SchofieldRhonda E. ColomboSusan E. ChambersRichard M. NovakAndrea WendrowSamir K. GuptaTida LeeTahaniyat LalaniMark HolodniyAarthi CharyNikhil HuprikarAnuradha GanesanNorio OhmagariAyako MikamiD. Ashley PriceChristopher J.A. DuncanKerry DierbergHenry J. NeumannStephanie N. TaylorAlisha LacourNajy MasriEdwin SwiatloKyle WidmerJames D. NeatonMary BessesenDavid S. StephensTimothy H. BurgessTimothy M. UyekiRobert WalkerG. Lynn MarksAnu OsinusiHuyen CaoAnabela CardosoStephanie de BonoDouglas E. SchlichtingKevin K. ChungJennifer L. FerreiraMichelle GreenMat MakowskiMichael R. WierzbickiTom M. ConradJill Ann El-KhorazatyHeather HillTyler BonnettNikki GettingerTheresa EngelTeri LewisJing WangJohn H. BeigelKay M. TomashekVarduhi GhazaryanTatiana BeresnevSeema NayakLori E. DoddWalla DempseyEffie NomicosMarina LeeRhonda Pikaart-TautgesMohamed ElsafyRobert JuraoHyung KooMichael ProschanTammy YokumJanice AregaRuth FloreseJocelyn D. VoellRichard DaveyRuth C. SerranoZanthia WileyVarun K. PhadkePaul A. GoepfertCarlos A. GomezTheresa A. SofarelliLaura CertainHannah N. ImlayCameron R. WolfeEmily R. KoJohn J. EngemannNora Bautista FelixClaire R. WanSammy T. ElmorLaurel R. BristowMichelle S. HarkinsNicole M. IovineMarie-Carmelle Elie-TurenneVictor F. TapsonPyoeng Gyun ChoeRichard A. MularskiKevin S. RhieRezhan H. HusseinDilek IncePatricia L. WinokurJin TakasakiSho SaitoKimberly McConnell, PharmDDavid L. WylesEllen SarconeKevin A. GrimesKatherine PerezCharles JanakJennifer A. WhitakerPaulina A. RebolledoJohn GharbinAllison A. LambertDiego F. ZeaEmma BainbridgeDavid C. HostlerJordanna M. HostlerBrian T. ShahanEvelyn LingMinjoung GoFleesie A. HubbardMelony ChakrabartyMaryrose Laguio-VilaEdward E. WalshFaheem GuirgisVincent C. MarconiChristian MadarScott A. BorgettiCorri LevineJoy NockKeith CandiottiJulia RozmanFernando DangondYann HyvertAndrea SeitzingerKaitlyn CrossStephanie PettiboneSeema U. NayakGregory A. Deye
EClinicalMedicine, Vol 69, Iss , Pp 102472- (2024)
Academic Journal
Menguy L; Laboratoire des Maladies Rénales Héréditaires, Institut Imagine, Inserm U1163, Université Paris Cité, Paris, France.; Hudier L; Service de Néphrologie, Centre Hospitalier Broussais, Saint Malo, France.; Zaidan M; Laboratoire des Maladies Rénales Héréditaires, Institut Imagine, Inserm U1163, Université Paris Cité, Paris, France.; Knebelmann B; APHP-Centre, Service de Néphrologie, Centre de Référence des Maladies Rénales Héréditaires de l'Enfant et de l'Adulte (MARHEA), Hôpital Universitaire Necker-Enfants malades, Paris, France.; Sayer JA; Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Central Parkway, Newcastle, UK; Renal Services, Newcastle Upon Tyne Hospitals NHS Foundation Trust, Newcastle, UK; NIHR Newcastle Biomedical Research Centre, Newcastle University, Newcastle upon Tyne, UK.; Arcila-Galvis J; Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Central Parkway, Newcastle, UK.; Arondel C; Laboratoire des Maladies Rénales Héréditaires, Institut Imagine, Inserm U1163, Université Paris Cité, Paris, France.; Hummel A; APHP-Centre, Service de Néphrologie, Centre de Référence des Maladies Rénales Héréditaires de l'Enfant et de l'Adulte (MARHEA), Hôpital Universitaire Necker-Enfants malades, Paris, France.; Dorval G; Laboratoire des Maladies Rénales Héréditaires, Institut Imagine, Inserm U1163, Université Paris Cité, Paris, France; APHP-Centre, Fédération de Génétique et Médecine Génomique, Service de Médecine Génomique des Maladies Rares, Hôpital Universitaire Necker-Enfants malades, Paris, France.; Morinière V; APHP-Centre, Fédération de Génétique et Médecine Génomique, Service de Médecine Génomique des Maladies Rares, Hôpital Universitaire Necker-Enfants malades, Paris, France.; Fula-Pitu L; Laboratoire des Maladies Rénales Héréditaires, Institut Imagine, Inserm U1163, Université Paris Cité, Paris, France.; Guerrera C; Platform for Proteomic Analyses, Structure Fédérative de Recherche Necker, INSERM US24/CNRS UAR 3633, Paris, France.; Buob D; APHP-Service d'Anatomie et Cytologie Pathologique, Hôpital Universitaire Tenon, Paris, France.; Rabeyrin M; Département d'Anatomopathologie, Hospices Civils de Lyon, Groupement Hospitalier Est, Bron, France.; Marijon P; Laboratoire de Biologie Médicale MultiSites SeqOIA, Paris, France.; Jean-Marcais N; Service de Génétique Clinique, Centre de Référence Anomalies du Développement et Syndromes Malformatifs de l'Inter-région Ouest, FHU GenOMedS, CHU Rennes Hôpital Sud, Rennes, France.; Fournier C; Service de Génétique Clinique, Plate-forme d'Expertise Maladies Rares-CHU Rennes Hôpital Sud, Rennes, France.; Duong Van Huyen JP; APHP-Centre, Service d'Anatomie Pathologique, Hôpital Universitaire Necker-Enfants malades, Paris, France.; Antignac C; Laboratoire des Maladies Rénales Héréditaires, Institut Imagine, Inserm U1163, Université Paris Cité, Paris, France.; Saunier S; Laboratoire des Maladies Rénales Héréditaires, Institut Imagine, Inserm U1163, Université Paris Cité, Paris, France.; Heidet L; Laboratoire des Maladies Rénales Héréditaires, Institut Imagine, Inserm U1163, Université Paris Cité, Paris, France; Laboratoire de Biologie Médicale MultiSites SeqOIA, Paris, France; APHP-Centre, Service de Néphrologie Pédiatrique, Centre de Référence des Maladies Rénales Héréditaires de l'Enfant et de l'Adulte (MARHEA), Hôpital Universitaire Necker-Enfants Malades, Paris, France. Electronic address: laurence.heidet@aphp.fr.
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
Academic Journal
Saei H; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.; Estebe B; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.; Goudin N; Necker Bioimage Analysis Core Facility of the Structure Fédérative de Recherche Necker, INSERM US24/CNRS UAR 3633, Paris, France.; Esmailpour M; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.; Haure J; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.; Gribouval O; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.; Arrondel C; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.; Moriniere V; Department of Genomic Medicine for Rare Diseases, Necker-Enfants Malades Hospital, Assistance publique, Hôpitaux de Paris (AP-HP), Paris, France.; Tian P; Wellcome Trust Centre for Cell-Matrix Research, University of Manchester, Manchester, United Kingdom.; Lennon R; Wellcome Trust Centre for Cell-Matrix Research, University of Manchester, Manchester, United Kingdom.; Department of Paediatric Nephrology, Royal Manchester Children's Hospital, Manchester University Hospitals NHS Foundation Trust, Manchester, United Kingdom.; Antignac C; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.; Mollet G; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.; Dorval G; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Université Paris Cité, Paris, France.; Department of Genomic Medicine for Rare Diseases, Necker-Enfants Malades Hospital, Assistance publique, Hôpitaux de Paris (AP-HP), Paris, France.
Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 101676073 Publication Model: eCollection Cited Medium: Internet ISSN: 2379-3708 (Electronic) Linking ISSN: 23793708 NLM ISO Abbreviation: JCI Insight Subsets: MEDLINE
Academic Journal
Petzold F; Division of Nephrology, Department of Endocrinology, Nephrology, and Rheumatology, University of Leipzig Medical Center, Leipzig, Germany.; Université Paris Cité, Imagine Institute, Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Paris, France.; Jeanpierre C; Université Paris Cité, Imagine Institute, Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Paris, France.; Chen X; Université Paris Cité, Imagine Institute, Data Science Platform, INSERM UMR1163, Paris, France.; Morinière V; APHP, Génétique Moléculaire, Hôpital Universitaire Necker-Enfants Malades, Paris, France.; Benmerah A; Université Paris Cité, Imagine Institute, Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Paris, France.; Dorval G; Université Paris Cité, Imagine Institute, Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Paris, France.; APHP, Génétique Moléculaire, Hôpital Universitaire Necker-Enfants Malades, Paris, France.; Saei H; Université Paris Cité, Imagine Institute, Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Paris, France.; Heidet L; Université Paris Cité, Imagine Institute, Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Paris, France.; APHP, Néphrologie Pédiatrique, Centre de Référence MARHEA, Hôpital Universitaire Necker-Enfants Malades, Paris, France.; Antignac C; Université Paris Cité, Imagine Institute, Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Paris, France.; Saunier S; Université Paris Cité, Imagine Institute, Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Paris, France.
Publisher: Wolters Kluwer Health Country of Publication: United States NLM ID: 101271570 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1555-905X (Electronic) Linking ISSN: 15559041 NLM ISO Abbreviation: Clin J Am Soc Nephrol Subsets: MEDLINE
Academic Journal
Le Moal P; Nephrology and Transplantation Department, Inherited Kidney Diseases Reference Center, Necker-Enfants Malades University Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.; Knebelmann B; Nephrology and Transplantation Department, Inherited Kidney Diseases Reference Center, Necker-Enfants Malades University Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.; Hummel A; Nephrology and Transplantation Department, Inherited Kidney Diseases Reference Center, Necker-Enfants Malades University Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.; Gribouval O; Inserm U1163, Laboratoire des Maladies Rénales Héréditaires, Imagine Institute, Université Paris Cité, Paris, France.; Anglicheau D; Nephrology and Transplantation Department, Inherited Kidney Diseases Reference Center, Necker-Enfants Malades University Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.; Legendre C; Nephrology and Transplantation Department, Inherited Kidney Diseases Reference Center, Necker-Enfants Malades University Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.; Morinière V; Genetic Department, Necker Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.; Heidet L; Inserm U1163, Laboratoire des Maladies Rénales Héréditaires, Imagine Institute, Université Paris Cité, Paris, France.; Pediatric Nephrology Department, Inherited Kidney Diseases Reference Center, Necker-Enfants Malades University Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.; Dorval G; Inserm U1163, Laboratoire des Maladies Rénales Héréditaires, Imagine Institute, Université Paris Cité, Paris, France.; Genetic Department, Necker Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.; Antignac C; Inserm U1163, Laboratoire des Maladies Rénales Héréditaires, Imagine Institute, Université Paris Cité, Paris, France.; Genetic Department, Necker Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.; Servais A; Nephrology and Transplantation Department, Inherited Kidney Diseases Reference Center, Necker-Enfants Malades University Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.; Inserm U1163, Laboratoire des Maladies Rénales Héréditaires, Imagine Institute, Université Paris Cité, Paris, France.
Publisher: Oxford University Press Country of Publication: England NLM ID: 101579321 Publication Model: eCollection Cited Medium: Print ISSN: 2048-8505 (Print) Linking ISSN: 20488505 NLM ISO Abbreviation: Clin Kidney J Subsets: PubMed not MEDLINE
Academic Journal
Marsili L; Université de Lille, ULR7364 RADEME, Hôpital Universitaire de Lille, Service de Génétique Clinique, Lille, France.; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.; Mantecon M; Institut Imagine, Genetics of Mitochondrial Diseases, Université Paris Cité, Inserm UMR 1163, Paris, France.; Arrondel C; Institut Imagine, Laboratory of Inherited Kidney Diseases, Université Paris Cité, Inserm UMR U1163, Paris, France.; Barcia G; Institut Imagine, Genetics of Mitochondrial Diseases, Université Paris Cité, Inserm UMR 1163, Paris, France.; APHP-Centre, Service de Médecine Génomique Des Maladies Rares, Hôpital Universitaire Necker-Enfants Malades, Paris, France.; Assouline Z; APHP-Centre, Service de Médecine Génomique Des Maladies Rares, Hôpital Universitaire Necker-Enfants Malades, Paris, France.; Gribouval O; Institut Imagine, Laboratory of Inherited Kidney Diseases, Université Paris Cité, Inserm UMR U1163, Paris, France.; Wellesley D; Wessex Clinical Genetics Service, University Hospital Southampton, Southampton, UK.; Harrison V; Wessex Clinical Genetics Service, University Hospital Southampton, Southampton, UK.; Marijon P; Laboratoire de Biologie Médicale MultiSites SeqOIA, Paris, France.; Colson C; Université de Lille, ULR7364 RADEME, Hôpital Universitaire de Lille, Service de Génétique Clinique, Lille, France.; Stichelbout M; Centre de Biologie-Pathologie de Lille, Hôpital Universitaire de Lille, Lille, France.; Gubler MC; Institut Imagine, Laboratory of Inherited Kidney Diseases, Université Paris Cité, Inserm UMR U1163, Paris, France.; Antignac C; Institut Imagine, Laboratory of Inherited Kidney Diseases, Université Paris Cité, Inserm UMR U1163, Paris, France.; Rotig A; Institut Imagine, Genetics of Mitochondrial Diseases, Université Paris Cité, Inserm UMR 1163, Paris, France.; Heidet L; Institut Imagine, Laboratory of Inherited Kidney Diseases, Université Paris Cité, Inserm UMR U1163, Paris, France. laurence.heidet@aphp.fr.; Laboratoire de Biologie Médicale MultiSites SeqOIA, Paris, France. laurence.heidet@aphp.fr.; APHP-Centre, Service de Néphrologie Pédiatrique, Centre de Référence Des Maladies Rénales Héréditaires de L'Enfant Et de L'Adulte (MARHEA), Hôpital Universitaire Necker-Enfants Malades, 149 Rue de Sèvres, 75015, Paris, France. laurence.heidet@aphp.fr.
Publisher: Springer International Country of Publication: Germany NLM ID: 8708728 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-198X (Electronic) Linking ISSN: 0931041X NLM ISO Abbreviation: Pediatr Nephrol Subsets: MEDLINE
Academic Journal
Torra R; Nephrology Department, Fundació Puigvert, Institut de Recerca Sant Pau (IR-Sant Pau), Departament de Medicina, Universitat Autònoma de Barcelona, RICORS2040, Barcelona, Spain.; Lipska-Zietkiewicz B; Clinical Genetics Unit, Department of Biology and Medical Genetics, Medical University of Gdańsk, Gdańsk, Poland.; Rare Diseases Centre, Medical University of Gdańsk, Gdańsk, Poland.; Acke F; Department of Otorhinolaryngology, 1P1, Ghent University / Ghent University Hospital, Ghent, Belgium.; Antignac C; Laboratory of Hereditary Kidney Diseases, Inserm UMR 1163, Imagine Institute, Université Paris Cite, Paris, France.; Becker JU; Institute of Pathology, University Hospital of Cologne, Cologne, Germany.; Cornec-Le Gall E; University Brest, Inserm, UMR 1078, GGB, CHU Brest, Centre de référence MARHEA, filière ORKID, Brest, France.; van Eerde AM; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Feltgen N; Department of Ophthalmology, University Hospital Basel, Basel, Switzerland.; Ferrari R; Italian Association of Alport Syndrome, (ASAL) ERKNet ePAG Castellarano, Emilia-Romaña, Italia.; Gale DP; Centre for Kidney and Bladder Health, University College London, London, UK.; Gear S; International Alport Syndrome Alliance and Alport UK, ERKNet ePAG, Cirencester, Gloucestershire, UK.; Gross O; Department of Nephrology and Rheumatology, University Medical Center Göttingen, Göttingen, Germany.; Haeberle S; Division of Paediatric Nephrology, Center for Paediatrics and Adolescent Medicine, University Hospital, Heidelberg, Germany.; Heidet L; Néphrologie Pédiatrique, Centre de Référence MARHEA, APHP, Hôpital universitaire Necker-Enfants Malades, Paris, France.; Lennon R; Department of Paediatric Nephrology, Royal Manchester Children's Hospital, Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.; Massella L; Division of Nephrology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.; Pfau K; Institute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.; Pizarro MDPV; Otolaryngology-Head and Neck Surgery, Hospital de Sant Pau i la Santa Creu, Instituto de Investigaciones Biomédicas Sant Pau, Universitat Autónoma de Barcelona, Barcelona, Spain.; Topaloglu R; Division of Pediatric Nephrology, Hacettepe University Faculty of Medicine, Ankara, Turkey.; Wlodkowski T; Division of Paediatric Nephrology, Center for Paediatrics and Adolescent Medicine, University Hospital, Heidelberg, Germany.; Zealey H; International Alport Syndrome Alliance and Alport UK, ERKNet ePAG, Cirencester, Gloucestershire, UK.
Publisher: Oxford University Press Country of Publication: England NLM ID: 8706402 Publication Model: Print Cited Medium: Internet ISSN: 1460-2385 (Electronic) Linking ISSN: 09310509 NLM ISO Abbreviation: Nephrol Dial Transplant Subsets: MEDLINE
Academic Journal
Mohammed Taha, HibaAalizadeh, RezaAlygizakis, NikiforosAntignac, Jean-PhilippeArp, Hans Peter H.Bade, RichardBaker, NancyBelova, LidiaBijlsma, LubertusBolton, Evan E.Brack, WernerCelma, AlbertoChen, Wen-LingCheng, TiejunChirsir, ParvielČirka, ĽubošD’Agostino, Lisa A.Djoumbou Feunang, YannickDulio, ValeriaFischer, StellanGago-Ferrero, PabloGalani, AikateriniGeueke, BirgitGłowacka, NataliaGlüge, JulianeGroh, KseniaGrosse, SylviaHaglund, PeterHakkinen, Pertti J.Hale, Sarah E.Hernandez, FelixJanssen, Elisabeth M.-L.Jonkers, TimKiefer, KarinKirchner, MichalKoschorreck, JanKrauss, MartinKrier, JessyLamoree, Marja H.Letzel, MarionLetzel, ThomasLi, QingliangLittle, JamesLiu, YannaLunderberg, David M.Martin, Jonathan W.McEachran, Andrew D.McLean, John A.Meier, ChristianeMeijer, JeroenMenger, FrankMerino, CarlaMuncke, JaneMuschket, MatthiasNeumann, MichaelNeveu, VanessaNg, KelseyOberacher, HerbertO’Brien, JakeOswald, PeterOswaldova, MartinaPicache, Jaqueline A.Postigo, CristinaRamirez, NoeliaReemtsma, ThorstenRenaud, JustinRostkowski, PawelRüdel, HeinzSalek, Reza M.Samanipour, SaerScheringer, MartinSchliebner, IvoSchulz, WolfgangSchulze, TobiasSengl, ManfredShoemaker, Benjamin A.Sims, KerrySinger, HeinzSingh, Randolph R.Sumarah, MarkThiessen, Paul A.Thomas, Kevin V.Torres, SoniaTrier, Xeniavan Wezel, Annemarie P.Vermeulen, Roel C. H.Vlaanderen, Jelle J.von der Ohe, Peter C.Wang, ZhanyunWilliams, Antony J.Willighagen, Egon L.Wishart, David S.Zhang, JianThomaidis, Nikolaos S.Hollender, JulianeSlobodnik, JaroslavSchymanski, Emma L.
Environmental Sciences Europe. 34(1)
Academic Journal
Gbadegesin R; Departments of Pediatrics and of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA.; Hinkes BGHoskins BEVlangos CNHeeringa SFLiu JLoirat COzaltin FHashmi SUlmer FCleper REttenger RAntignac CWiggins RCZenker MHildebrandt F
Publisher: Oxford University Press Country of Publication: England NLM ID: 8706402 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2385 (Electronic) Linking ISSN: 09310509 NLM ISO Abbreviation: Nephrol Dial Transplant Subsets: MEDLINE
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