부산대학교 도서관

Pampanos, Andreas ; Economides, John ; Iliadou, Vassiliki ; Neou, Polyxeni ; Leotsakos, Paulos ; Voyiatzis, Nikolaos ; Eleftheriades, Nikolaos ; Tsakanikos, Michael ; Antoniadi, Thalia ; Hatzaki, Angeliki ; Konstantopoulou, Irene ; Yannoukakos, Drakoulis ; Gronskov, Karen ; Brondum-Nielsen, Karen ; Grigoriadou, Maria ; Gyftodimou, Jolanda ; Iliades, Theophilos ; Skevas, Antonios ; Petersen, Michael B

In International Journal of Pediatric Otorhinolaryngology 2002 65(2):101-108

Velissariou, Voula; Antoniadi, Thalia; Gyftodimou, Jolanda; Bakou, Katerina; Grigoriadou, Maria; Christopoulou, Stavroula; Hatzipouliou, Athina; Donoghue, Jackie; Karatzis, Panagiotis; Katsarou, Efstathia; Petersen, Michael B

European Journal of Human Genetics. Nov2002, Vol. 10 Issue 11, p694. 5p.

Kitsos, George; Eiberg, Hans; Economou-Petersen, Effrosini; Wirtz, Mary K; Kramer, Patricia L; Aspiotis, Miltiadis; Tommerup, Niels; Petersen, Michael B; Psilas, Konstantinos

European Journal of Human Genetics. Jun2001, Vol. 9 Issue 6, p452. 6p.

Herlin, Morten K; Le, Vang Q; Højland, Allan T; Ernst, Anja; Okkels, Henrik; Petersen, Astrid C; Petersen, Michael B; Pedersen, Inge S

Human Reproduction. Sep2019, Vol. 34 Issue 9, p1838-1846. 9p. 2 Diagrams, 3 Charts.

Højland AT; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.; Research and Knowledge Center in Sensory Genetics, Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark.; Tavernier LJM; Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.; Schrauwen I; Center for Statistical Genetics, Department of Neurology, Gertrude H. Sergievsky Center, Columbia University Medical Center, New York, NY, USA.; Sommen M; Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.; Topsakal V; Department of ORL and Head and Neck Surgery, Antwerp University Hospital, University of Antwerp, Edegem, Belgium.; Schatteman I; European Institute for ORL, St-Augustinus Hospital Antwerp, Antwerp, Belgium.; Dhooge I; Department of Otolaryngology, Ghent University Hospital, Ghent, Belgium.; Huber A; Department of Otorhinolaryngology, Head and Neck Surgery, University Hospital Zurich, Zurich, Switzerland.; Zanetti D; Department of Clinical Sciences and Community Health, Audiology Unit, University of Milan, I.R.C.C.S. Fondazione 'Cà Granda', Osp.Le Maggiore Policlinico, Milano, Italy.; Kunst HPM; Department of Otorhinolaryngology, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, The Netherlands.; Department of Otorhinolaryngology, Maastricht University Medical Centre, Maastricht, The Netherlands.; Hoischen A; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Department of Otorhinolaryngology, Hearing and Genes, Radboud University Medical Center, Nijmegen, The Netherlands.; Department of Internal Medicine and Radboud Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, The Netherlands.; Petersen MB; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.; Research and Knowledge Center in Sensory Genetics, Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark.; Van Camp G; Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium. guy.vancamp@uantwerpen.be.; Fransen E; Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium. erik.fransen@uantwerpen.be.; StatUa Center for Statistics, University of Antwerp, Antwerp, Belgium. erik.fransen@uantwerpen.be.

Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE

Brix, Ninna; Jensen, Janni Majgaard; Pedersen, Inge Søkilde; Ernst, Anja; Frost, Simon; Bogaard, Pauline; Petersen, Michael B; Bender, Lars

Brix, N, Jensen, J M, Pedersen, I S, Ernst, A, Frost, S, Bogaard, P, Petersen, M B & Bender, L 2019, 'Mitochondrial Disease Caused by a Novel Homozygous Mutation (Gly106del) in the SCO1 Gene', Neonatology, vol. 116, no. 3, pp. 290–294. https://doi.org/10.1159/000499488

Lundsgaard, Malene; Le, Vang Q; Ernst, Anja; Laugaard-Jacobsen, Hans Christian; Rasmussen, Kirsten; Pedersen, Inge S; Petersen, Michael B

Lundsgaard, M, Le, V Q, Ernst, A, Laugaard-Jacobsen, H C, Rasmussen, K, Pedersen, I S & Petersen, M B 2017, 'De novo KAT6B Mutation Identified with Whole-Exome Sequencing in a Girl with Say-Barber/Biesecker/Young-Simpson Syndrome', Molecular Syndromology, vol. 8, no. 1, pp. 24-29. https://doi.org/10.1159/000452258

Assia Batzir N; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Texas Children's Hospital, Houston, Texas.; Kishor Bhagwat P; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, Texas.; Larson A; Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado School of Medicine, Aurora, Colorado.; Coban Akdemir Z; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Bagłaj M; Department of Pediatric Surgery and Urology, Wroclaw Medical University, Wroclaw, Poland.; Bofferding L; Département de Pédiatrie Néonatologie, Kannerklinik, Centre Hospitalier de Luxembourg, Luxembourg City, Luxembourg.; Bosanko KB; Section of Genetics and Metabolism, University of Arkansas for Medical Sciences, Little Rock, Arkansas.; Bouassida S; Humboldt Clinic, Vivantes Health Network GmbH, Charité Academic Teaching Hospital, Medical University of Berlin, Berlin, Germany.; Callewaert B; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Department of Biomolecular Medicine, Ghent University Hospital, Ghent, Belgium.; Cannon A; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama.; Enchautegui Colon Y; Inherited Metabolic Diseases Clinic, Section of Clinical Genetics and Metabolism, University of Colorado Denver, Aurora, Colorado.; Garnica AD; Section of Genetics and Metabolism, University of Arkansas for Medical Sciences, Little Rock, Arkansas.; Harr MH; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.; Heck S; Département de Pédiatrie Néonatologie, Kannerklinik, Centre Hospitalier de Luxembourg, Luxembourg City, Luxembourg.; Hurst ACE; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama.; Jhangiani SN; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.; Isidor B; CHU de Nantes, Service de Génétique Médicale, Nantes 44093 Cedex 1, Nantes, France.; Littlejohn RO; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Department of Pediatrics, Baylor College of Medicine, San Antonio, Texas.; Liu P; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Magoulas P; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Texas Children's Hospital, Houston, Texas.; Mar Fan H; Genetic Health Queensland, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.; Marom R; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Texas Children's Hospital, Houston, Texas.; McLean S; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Department of Pediatrics, Baylor College of Medicine, San Antonio, Texas.; Nezarati MM; Genetics Program, North York General Hospital, University of Toronto, Toronto, Ontario, Canada.; Nugent KM; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Department of Pediatrics, Baylor College of Medicine, San Antonio, Texas.; Petersen MB; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.; Rocha ML; Humboldt Clinic, Vivantes Health Network GmbH, Charité Academic Teaching Hospital, Medical University of Berlin, Berlin, Germany.; Roeder E; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Department of Pediatrics, Baylor College of Medicine, San Antonio, Texas.; Smigiel R; Department of Pediatrics, Division of Pediatrics and Rare Disorders, Wroclaw Medical University, Wroclaw, Poland.; Tully I; Genetic Health Queensland, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.; Weisfeld-Adams J; Inherited Metabolic Diseases Clinic, Section of Clinical Genetics and Metabolism, University of Colorado Denver, Aurora, Colorado.; Wells KO; Department of Surgery, Division of Colorectal Surgery, Baylor University Medical Center, Dallas, Texas.; Posey JE; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Lupski JR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Texas Children's Hospital, Houston, Texas.; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.; Department of Pediatrics, Baylor College of Medicine, Houston, Texas.; Beaudet AL; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Texas Children's Hospital, Houston, Texas.; Department of Pediatrics, Baylor College of Medicine, Houston, Texas.; Wangler MF; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.; Texas Children's Hospital, Houston, Texas.; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, Texas.; Department of Pediatrics, Baylor College of Medicine, Houston, Texas.

Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE

Johannesen KM; Department of Epilepsy Genetics and Personalized Treatment, Danish Epilepsy Center Filadelfia, Dianalund, Denmark.; Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark.; Gardella E; Department of Epilepsy Genetics and Personalized Treatment, Danish Epilepsy Center Filadelfia, Dianalund, Denmark.; Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark.; Encinas AC; Graduate Interdisciplinary Program of Genetics, University of Arizona, Tucson, Arizona.; Lehesjoki AE; Folkhälsan Research Center, Helsinki, Finland.; Research Programs Unit, Molecular Neurology and Medicum, University of Helsinki, Helsinki, Finland.; Linnankivi T; Department of Child Neurology, Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Petersen MB; Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark.; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.; Lund ICB; Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark.; Blichfeldt S; Department of Pediatrics, Herlev Hospital, Herlev, Denmark.; Miranda MJ; Department of Pediatrics, Herlev Hospital, Herlev, Denmark.; Pal DK; Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology, and Neuroscience, King's College London, London, UK.; King's College Hospital, London, UK.; Evelina London Children's Hospital, London, UK.; Medical Research Council Centre for Neurodevelopmental Disorders, King's College, London, UK.; Lascelles K; Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology, and Neuroscience, King's College London, London, UK.; Procopis P; Children's Hospital, Westmead, Sydney, New South Wales, Australia.; Discipline of Child and Adolescent Health, Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.; Orsini A; Pediatric Neurology, Pediatric Clinic, University of Pisa, Pisa, Italy.; Bonuccelli A; Pediatric Neurology, Pediatric Clinic, University of Pisa, Pisa, Italy.; Giacomini T; Child Neuropsychiatry Unit, Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, and Maternal and Children's Sciences, Giannina Gaslini Institute, University of Genoa, Genoa, Italy.; Helbig I; Department of Neuropediatrics, University Medical Center Schleswig Holstein, Kiel, Germany.; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.; Fenger CD; Department of Epilepsy Genetics and Personalized Treatment, Danish Epilepsy Center Filadelfia, Dianalund, Denmark.; Sisodiya SM; Department of Clinical and Experimental Epilepsy, University College London Institute of Neurology, London, UK.; Chalfont Centre for Epilepsy, Bucks, UK.; Hernandez-Hernandez L; Department of Clinical and Experimental Epilepsy, University College London Institute of Neurology, London, UK.; Chalfont Centre for Epilepsy, Bucks, UK.; Krithika S; Department of Clinical and Experimental Epilepsy, University College London Institute of Neurology, London, UK.; Chalfont Centre for Epilepsy, Bucks, UK.; Rumple M; Pediatric Neurology, Banner Children's Specialists, Glendale, Arizona.; Masnada S; Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.; Valente M; Genomic and Postgenomic Center, Scientific Institute for Research and Healthcare (IRCCS) Mondino Foundation, Pavia, Italy.; Cereda C; Genomic and Postgenomic Center, Scientific Institute for Research and Healthcare (IRCCS) Mondino Foundation, Pavia, Italy.; Giordano L; Child Neurology and Psychiatry Unit, Civilian Hospital, Brescia, Italy.; Accorsi P; Child Neurology and Psychiatry Unit, Civilian Hospital, Brescia, Italy.; Bürki SE; Department of Pediatrics, Division of Child Neurology, University Children's Hospital Bern, University of Bern, Bern, Switzerland.; Mancardi M; Unit of Child Neuropsychiatry, Epilepsy Center, Department of Clinical and Surgical Neuroscience and Rehabilitation, Giannina Gaslini Institute, Genoa, Italy.; Korff C; Child Neurology Unit, University Children's Hospital, Geneva, Switzerland.; Guerrini R; Neuroscience Department, Children's Hospital Anna Meyer, University of Florence, Florence, Italy.; von Spiczak S; Department of Neuropediatrics, Christian Albrecht University, Kiel, Germany.; Northern German Epilepsy Center for Children and Adolescents, Schwentinental, Germany.; Hoffman-Zacharska D; Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland.; Mazurczak T; Department of Neurology of Children and Adolescents, Institute of Mother and Child, Warsaw, Poland.; Coppola A; Department of Neuroscience and Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy.; Buono S; Neurology Division, Hospital of National Relevance (AORN), Santobono Pausilipon, Naples, Italy.; Vecchi M; Pediatric Clinic, Hospital Company, University of Padua, Padua, Italy.; Hammer MF; University of Arizona Genetic Core, University of Arizona, Tucson, Arizona.; Varesio C; Brain and Behavior Department, University of Pavia, Pavia, Italy.; Child and Adolescence Neurology Department, IRCCS C. Mondino National Neurological Institute, Pavia, Italy.; Veggiotti P; Department of Child Neurology, V. Buzzi Children's Hospital, Milan, Italy.; L. Sacco Department of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.; Lal D; Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, Ohio.; Genomic Medicine Institute, Lerner Research Institute Cleveland Clinic, Cleveland, Ohio.; Stanley Center for Psychiatric Research, Broad Institute of Massachusetts Institute of Technology and Harvard, Cambridge, Massachusetts.; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts.; Cologne Center for Genomics, University of Cologne, Cologne, Germany.; Brünger T; Cologne Center for Genomics, University of Cologne, Cologne, Germany.; Zara F; Laboratory of Neurogenetics and Neuroscience, Department of Head-Neck and Neuroscience, Giannina Gaslini Institute, Genoa, Italy.; Striano P; Pediatric Neurology, Pediatric Clinic, University of Studies of Pisa, Pisa, Italy.; Rubboli G; Department of Epilepsy Genetics and Personalized Treatment, Danish Epilepsy Center Filadelfia, Dianalund, Denmark.; University of Copenhagen, Copenhagen, Denmark.; Møller RS; Department of Epilepsy Genetics and Personalized Treatment, Danish Epilepsy Center Filadelfia, Dianalund, Denmark.; Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark.

Publisher: Blackwell Science Country of Publication: United States NLM ID: 2983306R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-1167 (Electronic) Linking ISSN: 00139580 NLM ISO Abbreviation: Epilepsia Subsets: MEDLINE

Sarri, Catherine; Douzgou, Sofia; Kontos, Haris; Anagnostopoulou, Katherine; Tümer, Zeynep; Grigoriadou, Maria; Petersen, Michael B; Kokotas, Haris; Merou, Konstantina; Pandelia, Efi; Giouroukou, Elena; Papanikolaou, Katerina; Côté, Gilbert B; Gyftodimou, Yolanda

Cytogenetic and Genome Research. 145:6-13

Chiras, Dimitrios; Kitsos, George; Petersen, Michael B; Skalidakis, Iosif; Kroupis, Christos

Chiras, D, Kitsos, G, Petersen, M B, Skalidakis, I & Kroupis, C 2015, 'Oxidative stress in dry age-related macular degeneration and exfoliation syndrome', Critical Reviews in Clinical Laboratory Sciences, vol. 52, no. 1, pp. 12-27. https://doi.org/10.3109/10408363.2014.968703

Antoniadi, Thalia; Rabionet, Raquel; Kroupis, Christos; Aperis, George A; Economides, John; Petmezakis, Jacob; Economou-Petersen, Effrosini; Estivill, Xavier; Petersen, Michael B

Clinical Genetics. May 01, 1999 55(5):381-382

Tekin, Mustafa; Chioza, Barry A; Matsumoto, Yoshifumi; Diaz-Horta, Oscar; Cross, Harold E; Duman, Duygu; Kokotas, Haris; Moore-Barton, Heather L; Sakoori, Kazuto; Ota, Maya; Odaka, Yuri S; Foster, Joseph; Cengiz, F Basak; Tokgoz-Yilmaz, Suna; Tekeli, Oya; Grigoriadou, Maria; Petersen, Michael B; Sreekantan-Nair, Ajith; Gurtz, Kay; Xia, Xia-Juan; Pandya, Arti; Patton, Michael A; Young, Juan I; Aruga, Jun; Crosby, Andrew H

Tekin, M, Chioza, B A, Matsumoto, Y, Diaz-Horta, O, Cross, H E, Duman, D, Kokotas, H, Moore-Barton, H L, Sakoori, K, Ota, M, Odaka, Y S, Foster, J, Cengiz, F B, Tokgoz-Yilmaz, S, Tekeli, O, Grigoriadou, M, Petersen, M B, Sreekantan-Nair, A, Gurtz, K, Xia, X-J, Pandya, A, Patton, M A, Young, J I, Aruga, J & Crosby, A H 2013, 'SLITRK6 mutations cause myopia and deafness in humans and mice', Journal of Clinical Investigation, vol. 123, no. 5, pp. 2094-2102. https://doi.org/10.1172/JCI65853

Hansen, Claus; Bugge, Merete; Brandt, Carsten A; Hertz, Jens M; Tranebjœrg, Lisbeth; Mikkelsen, Margareta; Petersen, Michael B

Clinical Genetics. Apr 01, 1998 53(4):321-322

Sarri, Catherine; Douzgou, Sofia; Gyftodimou, Yolanda; Tümer, Zeynep; Ravn, Kirstine; Pasparaki, Angela; Sarafidou, Theologia; Kontos, Harry; Kokotas, Haris; Karadima, Georgia; Grigoriadou, Maria; Pandelia, Effie; Theodorou, Virginia; Moschonas, Nicholas K; Petersen, Michael B

American Journal of Medical Genetics Part A. 155:2841-2854

Kokotas, Haris; Grigoriadou, Maria; Yang, Li; Lodahl, Marianne; Rendtorff, Nanna Dahl; Gyftodimou, Yolanda; Korres, George S; Ferekidou, Elisabeth; Kandiloros, Dimitrios; Korres, Stavros; Tranebjærg, Lisbeth; Guan, Min-Xin; Petersen, Michael B; Li, Yang; Petersen, Michael Bang

International Journal of Pediatric Otorhinolaryngology. 75:89-94

Papoulidis I; Access to Genome P.C., Clinical Laboratory Genetics, Lampsakou 11, 11528 Thessaloniki, Greece.; Eleftheriades M; Second Department of Obstetrics and Gynaecology, Aretaieion Hospital, Medical School, National and Kapodistrian University of Athens, 112527 Athens, Greece.; Manolakos E; Access to Genome P.C., Clinical Laboratory Genetics, Lampsakou 11, 11528 Thessaloniki, Greece.; Department of Medical Genetics, University of Cagliari, Binaghi Hospital, 09124 Cagliari, Italy.; Petersen MB; Access to Genome P.C., Clinical Laboratory Genetics, Lampsakou 11, 11528 Thessaloniki, Greece.; Liappi SM; Access to Genome P.C., Clinical Laboratory Genetics, Lampsakou 11, 11528 Thessaloniki, Greece.; Konstantinidou A; 1st Department of Pathology, School of Medicine, National and Kapodistrian University of Athens, 11528 Athens, Greece.; Papamichail M; Postgraduate Programme 'Maternal Fetal Medicine', Medical School, National and Kapodistrian University of Athens, 11528 Athens, Greece.; Papadopoulos V; Department of Obstetrics & Gynecology, University of Patra, 26500 Patras, Greece.; Garas A; Department of Gynecology, Larissa Medical School, University of Thessaly, 38221 Larissa, Greece.; Sotiriou S; Department of Clinical Embryology, Larissa Medical School, University of Thessaly, 41334 Larissa, Greece.; Papastefanou I; Fetal Medicine Clinic, Monis Petraki 4, Kolonaki, 11521 Athens, Greece.; Daskalakis G; First Department of Obstetrics and Gynaecology, 'Alexandra' Maternity Hospital, Medical School, National and Kapodistrian University of Athens, 15772 Athens, Greece.; Ristic A; Obstetric and Gynecological Clinic Narodni Front, 11000 Belgrade, Serbia.

Publisher: MDPI AG Country of Publication: Switzerland NLM ID: 101648936 Publication Model: Electronic Cited Medium: Print ISSN: 2227-9067 (Print) Linking ISSN: 22279067 NLM ISO Abbreviation: Children (Basel) Subsets: PubMed not MEDLINE

Majava, Marja; Hoornaert, Kristien P; Bartholdi, Deborah; Bouma, Mieke C; Bouman, Katelijne; Carrera, Marta; Devriendt, Koenraad; Hurst, Jane; Kitsos, George; Niedrist, Dunja; Petersen, Michael B; Shears, Debbie; Stolte-Dijkstra, Irene; Van Hagen, J M; Ala-Kokko, Leena; Männikkö, Minna; Mortier, Geert R

American Journal of Medical Genetics Part A. :258-264

Højland AT; Research and Knowledge Center in Sensory Genetics, Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark.; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.; Lolas I; Research and Knowledge Center in Sensory Genetics, Section of Molecular Diagnostics, Department of Clinical Biochemistry, Aalborg University Hospital, Aalborg, Denmark.; Okkels H; Research and Knowledge Center in Sensory Genetics, Section of Molecular Diagnostics, Department of Clinical Biochemistry, Aalborg University Hospital, Aalborg, Denmark.; Lautrup CK; Research and Knowledge Center in Sensory Genetics, Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark.; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.; Diness BR; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen.; Petersen MB; Research and Knowledge Center in Sensory Genetics, Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark.; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.; Nielsen IK; Research and Knowledge Center in Sensory Genetics, Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark.

Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

Chelban V; Department of Molecular Neuroscience, University College London, Institute of Neurology, London, UK.; National Hospital for Neurology and Neurosurgery, London, UK.; Department of Neurology and Neurosurgery, Institute of Emergency Medicine, Chisinau, Republic of Moldova.; Wiethoff S; Department of Molecular Neuroscience, University College London, Institute of Neurology, London, UK.; Center for Neurology and Hertie Institute for Clinical Brain Research, Eberhard-Karls-University, Tübingen, Germany.; Fabian-Jessing BK; Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark.; Haridy NA; Department of Molecular Neuroscience, University College London, Institute of Neurology, London, UK.; Department of Neurology and Psychiatry, Assiut University Hospital, Faculty of Medicine, Assiut, Egypt.; Khan A; Department of Molecular Neuroscience, University College London, Institute of Neurology, London, UK.; Efthymiou S; Department of Molecular Neuroscience, University College London, Institute of Neurology, London, UK.; Becker EBE; Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.; O'Connor E; Department of Molecular Neuroscience, University College London, Institute of Neurology, London, UK.; Hersheson J; Department of Molecular Neuroscience, University College London, Institute of Neurology, London, UK.; Newland K; Department of Molecular Neuroscience, University College London, Institute of Neurology, London, UK.; Hojland AT; Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark.; Gregersen PA; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.; Lindquist SG; Danish Dementia Research Centre, Neurogenetics Clinic, Department of Neurology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.; Department of Clinical Genetics, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.; Petersen MB; Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark.; Nielsen JE; Danish Dementia Research Centre, Neurogenetics Clinic, Department of Neurology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.; Nielsen M; Department of Neurology, Aalborg University Hospital, Aalborg, Denmark.; Wood NW; Department of Molecular Neuroscience, University College London, Institute of Neurology, London, UK.; National Hospital for Neurology and Neurosurgery, London, UK.; Giunti P; Deparmtent of Molecular Neuroscience, Ataxia Centre UCL, Institute of Neurology, London, UK.; Houlden H; Department of Molecular Neuroscience, University College London, Institute of Neurology, London, UK.; National Hospital for Neurology and Neurosurgery, London, UK.

Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8257 (Electronic) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord