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The natural history of Canavan disease: 23 new cases and comparison with patients from literature.
Bley, Annette; Denecke, Jonas; Kohlschütter, Alfried; Schön, Gerhard; Hischke, Sandra; Guder, Philipp; Bierhals, Tatjana; Lau, Heather; Hempel, Maja; Eichler, Florian S.
Afiliación
  • Bley A; Department of Pediatrics, University Medical Center Hamburg Eppendorf, Martini-Str. 52, 20246, Hamburg, Germany. abley@uke.de.
  • Denecke J; Department of Pediatrics, University Medical Center Hamburg Eppendorf, Martini-Str. 52, 20246, Hamburg, Germany.
  • Kohlschütter A; Department of Pediatrics, University Medical Center Hamburg Eppendorf, Martini-Str. 52, 20246, Hamburg, Germany.
  • Schön G; Institute of Medical Biometry and Epidemiology, University Medical Center Hamburg Eppendorf, Martini-Str. 52, 20246, Hamburg, Germany.
  • Hischke S; Institute of Medical Biometry and Epidemiology, University Medical Center Hamburg Eppendorf, Martini-Str. 52, 20246, Hamburg, Germany.
  • Guder P; Department of Pediatrics, University Medical Center Hamburg Eppendorf, Martini-Str. 52, 20246, Hamburg, Germany.
  • Bierhals T; Department of Human Genetics, University Medical Center Hamburg Eppendorf, Martini-Str. 52, 20246, Hamburg, Germany.
  • Lau H; Department of Neurogenetics, NYU, 222 East 41st Street, New York, NY, 10017, USA.
  • Hempel M; Department of Human Genetics, University Medical Center Hamburg Eppendorf, Martini-Str. 52, 20246, Hamburg, Germany.
  • Eichler FS; Department of Neurology, MGH, Harvard Medical School, 55 Fruit St, Boston, MA, 02114, USA.
Orphanet J Rare Dis ; 16(1): 227, 2021 05 19.
Article en En | MEDLINE | ID: mdl-34011350
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Canavan Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans / Infant Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2021 Tipo del documento: Article País de afiliación: Alemania
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Canavan Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans / Infant Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2021 Tipo del documento: Article País de afiliación: Alemania