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CHRONIC GM2 GANGLIOSIDOSIS MASQUERADING AS ATYPICAL FRIEDREICH ATAXIA: CLINICAL, MORPHOLOGIC, AND BIOCHEMICAL STUDIES OF NINE CASES

Author
WILLNER JP; GRABOWSKI GA; GORDON RE; BENDER AN; DESNICK RJ
MOUNT SINAI SCH. MED./NEW YORK NY 10029/USA
Source
NEUROLOGY; ISSN 0028-3878; USA; DA. 1981; VOL. 31; NO 7; PP. 787-798; BIBL. 44 REF.
Document type
Article
Language
English
Keyword (fr)
HEREDODEGENERATION SPINOCEREBELLEUSE FRIEDREICH ATYPIQUE SPHINGOLIPIDOSE HEREDITAIRE TAY SACHS DIAGNOSTIC DIFFERENTIEL SYSTEME NERVEUX PATHOLOGIE METABOLISME PATHOLOGIE MALADIE HEREDITAIRE LIPIDE ENFANT ADULTE HOMME NEUROLOGIE MALADIES METABOLIQUES
Keyword (en)
FRIEDREICH ATAXIA ATYPICAL TAY SACHS DISEASE DIFFERENTIAL DIAGNOSTIC NERVOUS SYSTEM DISEASES METABOLIC DISEASES GENETIC DISEASE LIPIDS CHILD ADULT HUMAN NEUROLOGY METABOLIC DISEASES
Keyword (es)
NEUROLOGIA ENFERMEDADES METABOLICAS
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology

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

Discipline
Endocrinopathies Neurology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
PASCAL8110457010

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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