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Corrigendum to: Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes.
Himmelreich, Nastassja; Bertoldi, Mariarita; Alfadhel, Majid; Alghamdi, Malak Ali; Anikster, Yair; Bao, Xinhua; Bashiri, Fahad A; Zeev, Bruria Ben; Bisello, Giovanni; Ceylan, Ahmet Cevdet; Chien, Yin-Hsiu; Choy, Yew Sing; Elsea, Sarah H; Flint, Lisa; García-Cazorla, Àngels; Gijavanekar, Charul; Gümüs, Emel Yilmaz; Hamad, Muddathir H; Hismi, Burcu; Honzik, Tomas; Kuseyri Hübschmann, Oya; Hwu, Wuh-Liang; Ibáñez-Micó, Salvador; Jeltsch, Kathrin; Juliá-Palacios, Natalia; Kasapkara, Çigdem Seher; Kurian, Manju A; Kusmierska, Katarzyna; Liu, Ning; Ngu, Lock Hock; Odom, John D; Ong, Winnie Peitee; Opladen, Thomas; Oppeboen, Mari; Pearl, Phillip L; Pérez, Belén; Pons, Roser; Rygiel, Agnieszka Magdalena; Shien, Tan Ee; Spaull, Robert; Sykut-Cegielska, Jolanta; Tabarki, Brahim; Tangeraas, Trine; Thöny, Beat; Wassenberg, Tessa; Wen, Yongxin; Yakob, Yusnita; Yin, Jasmine Goh Chew; Zeman, Jiri; Blau, Nenad.
Afiliación
  • Himmelreich N; Dietmar-Hopp Metabolic Center and Centre for Pediatrics and Adolescent Medicine, University Children's Hospital, Heidelberg, Germany.
  • Bertoldi M; Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
  • Alfadhel M; Medical Genomic Research Department, King Abdullah International Medical Research Center (KAIMRC), King Saud Bin Abdulaziz University for Health Sciences, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia; Genetics and Precision Medicine Department, King Abdullah Specialized Children's
  • Alghamdi MA; Medical Genetic Division, Pediatric Department, College of Medicine, King Saud University, Riyadh, SA, Saudi Arabia.
  • Anikster Y; Metabolic Disease Unit, The Edmond and Lily Safra Childrens Hospital, Sheba Medical Center, Tel Hashomer, Sackler School of Medicine, Tel Aviv University, Israel.
  • Bao X; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Bashiri FA; Division of Neurology, Department of Pediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
  • Zeev BB; Pediatric Neurology, Safra Pediatric Hospital, Sheba Medical Center, Sackler School of Medicine, Tel Aviv University, Ramat Gan, Israel.
  • Bisello G; Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
  • Ceylan AC; Ankara Yildirim Beyazit University, Department of Medical Genetics, Ankara Bilkent City Hospital, Ankara, Turkey.
  • Chien YH; Department of Medical Genetics & Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
  • Choy YS; Prince Court Medical Center, Kuala Lumpur, Malaysia.
  • Elsea SH; Dept. of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Flint L; AADC Research Trust, Surrey, UK.
  • García-Cazorla À; Neurometabolic Unit, Department of Neurology, Hospital Sant Joan de Déu, CIBERER, Barcelona, Spain.
  • Gijavanekar C; Dept. of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Gümüs EY; Department of Pediatrics and Inherited Metabolic Diseases, Marmara University School of Medicine, Istanbul, Turkey.
  • Hamad MH; Neurology Division, Pediatric Department, King Saud University Medical City, Riyadh, SA, Saudi Arabia.
  • Hismi B; Department of Pediatrics and Inherited Metabolic Diseases, Marmara University School of Medicine, Istanbul, Turkey.
  • Honzik T; Dept. of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Kuseyri Hübschmann O; Dietmar-Hopp Metabolic Center and Centre for Pediatrics and Adolescent Medicine, University Children's Hospital, Heidelberg, Germany; Division of Neuropediatrics and Metabolic Medicine, University Children's Hospital Heidelberg, Heidelberg, Germany.
  • Hwu WL; Department of Medical Genetics & Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
  • Ibáñez-Micó S; Pediatric Neurology Unit, Arrixaca Universitary Hospital, 30120 Murcia, Spain.
  • Jeltsch K; Division of Neuropediatrics and Metabolic Medicine, University Children's Hospital Heidelberg, Heidelberg, Germany.
  • Juliá-Palacios N; Neurometabolic Unit, Department of Neurology, Hospital Sant Joan de Déu, CIBERER, Barcelona, Spain.
  • Kasapkara ÇS; Department of Pediatric Metabolism, Ankara Yildirim Beyazit University, Ankara Bilkent City Hospital, Ankara, Turkey.
  • Kurian MA; Developmental Neurosciences, Zayed Centre for Research, UCL GOS-Institute of Child Health & Department of Neurology, Great Ormond Street Hospital, London, United Kingdom.
  • Kusmierska K; Department of Screening and Metabolic Diagnostics, Institute of Mother and Child, Warsaw, Poland.
  • Liu N; Dept. of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Ngu LH; Department of Genetics, Hospital Kuala Lumpur, Ministry of Health, Malaysia.
  • Odom JD; Dept. of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Ong WP; Department of Genetics, Hospital Kuala Lumpur, Ministry of Health, Malaysia.
  • Opladen T; Division of Neuropediatrics and Metabolic Medicine, University Children's Hospital Heidelberg, Heidelberg, Germany.
  • Oppeboen M; Children's Department, Division of Child Neurology and Norwegian National Unit for Newborn Screening, Division of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
  • Pearl PL; Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Pérez B; Centro de Diagnostico de Enfermedades Moleculares, CIBERER, IdiPAZ, Universidad Autonoma de Madrid, Madrid, Spain.
  • Pons R; First Department of Pediatrics, Aghia Sophia Children's Hospital, University of Athens, Athens, Greece.
  • Rygiel AM; Department of Medical Genetics, Laboratory of Hereditary Diseases, Institute of Mother and Child, Warsaw, Poland.
  • Shien TE; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital, Singapore.
  • Spaull R; Developmental Neurosciences, Zayed Centre for Research, UCL GOS-Institute of Child Health & Department of Neurology, Great Ormond Street Hospital, London, United Kingdom.
  • Sykut-Cegielska J; Department of Inborn Errors of Metabolism and Paediatrics, The Institute of Mother and Child, Warsaw, Poland.
  • Tabarki B; Division of Neurology, Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • Tangeraas T; Norwegian National Unit for Newborn Screening, Division of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
  • Thöny B; Divisions of Metabolism, University Children's Hospital, Zürich, Switzerland.
  • Wassenberg T; UZ Brussel, Department of Pediatrics, Brussels, Belgium.
  • Wen Y; Medical Genetic Division, Pediatric Department, College of Medicine, King Saud University, Riyadh, SA, Saudi Arabia.
  • Yakob Y; Molecular Diagnostics Unit, Specialised Diagnostics Centre, Institute for Medical Research, National Institute of Health, Ministry of Health, Malaysia.
  • Yin JGC; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital, Singapore.
  • Zeman J; Dept. of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Blau N; Divisions of Metabolism, University Children's Hospital, Zürich, Switzerland. Electronic address: nenad.blau@kispi.uzh.ch.
Mol Genet Metab ; 139(4): 107647, 2023 Aug.
Article en En | MEDLINE | ID: mdl-37453860
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prevalence_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2023 Tipo del documento: Article País de afiliación: Alemania
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prevalence_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2023 Tipo del documento: Article País de afiliación: Alemania