SYSTEMIC CARNITINE DEFICIENCY: A TREATABLE INHERITED LIPID-STORAGE DISEASE PRESENTING AS REYE'S SYNDROME
- Author
- CHAPOY PR; ANGELINI C; BROWN WJ; STIFF JE; SHUG AL; CEDERBAUM SD
UNIV. CALIFORNIA, CENT. HEALTH SCI./LOS ANGELES CA 90024/USA - Source
- N. ENGL. J. MED.; ISSN 0028-4793; USA; DA. 1980; VOL. 303; NO 24; PP. 1389-1394; BIBL. 30 REF.
- Document type
- Article
- Language
- English
- Keyword (fr)
- REYE SYNDROME DEFICIT CARNITINE TRAITEMENT ENFANT HOMME METABOLISME PATHOLOGIE LIPIDE MALADIES METABOLIQUES
- Keyword (en)
- REYE SYNDROME DEFICIENCY CARNITINE TREATMENT CHILD HUMAN METABOLIC DISEASES LIPIDS METABOLIC DISEASES
- Keyword (es)
- ENFERMEDADES METABOLICAS
- Classification
- Discipline
- Endocrinopathies
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- PASCAL8110427067
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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