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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
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B21 Endocrinopathies

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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