Lysosomal Storage Disease 1 Phenotype, diagnosis, and treatment of Gaucher's disease
- Author
- GRABOWSKI, Gregory A1
[1] Cincinnati Children's Hospital Medical Center, Division of Human Genetics, Department of Pediatrics, University of Cincinnati, Cincinnati, OH, United States - Source
Lancet (British edition). 2008, Vol 372, Num 9645, pp 1263-1271, 9 p ; ref : 107 ref
- CODEN
- LANCAO
- ISSN
- 0140-6736
- Scientific domain
- General medicine general surgery
- Publisher
- Lancet, London
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Diagnostic Lipide Médecine Pathologie des lysosomes Phénotype Sphingolipidose héréditaire de Gaucher Traitement Enzymopathie Lipoïdose Maladie héréditaire Maladie métabolique Pathologie de l'encéphale Pathologie du système nerveux central Pathologie du système nerveux
- Keyword (en)
- Diagnosis Lipids Medicine Lysosomal storage disease Phenotype Gaucher disease Treatment Enzymopathy Lipoidosis Genetic disease Metabolic diseases Cerebral disorder Central nervous system disease Nervous system diseases
- Keyword (es)
- Diagnóstico Lípido Medicina Lisosoma patología Fenotipo Esfingolipidosis hereditaria Gaucher Tratamiento Enzimopatía Lipoidosis Enfermedad hereditaria Metabolismo patología Encéfalo patología Sistema nervosio central patología Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22D Errors of metabolism / 002B22D02 Lipids (lysosomal enzyme disorders, storage diseases)
- Discipline
- Generalities in medical sciences Metabolic diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 20667869
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1016/S0140-6736(08)61522-6 
https://dx.doi.org/10.1016/S0140-6736(08)61522-6
