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The cherry-red spot in tay-sachs and other storage diseases

Author
KIVLIN, J. D1 ; SANBORN, G. E; MYERS, G. G
[1] Univ. Utah, medical center, Salt Lake City UT 84132, United States
Source

Annals of neurology. 1985, Vol 17, Num 4, pp 356-360 ; ref : 41 ref

CODEN
ANNED3
ISSN
0364-5134
Scientific domain
Neurology
Publisher
Willey-Liss, Hoboken
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Gangliosidose GM1 Homme Lipide Lipomucopolysaccharidose Maladie héréditaire Métabolisme pathologie Sphingolipidose héréditaire Niemann Pick Sphingolipidose héréditaire Tay Sachs Tache rouge cerise Thésaurismose
Keyword (en)
GM1 gangliosidosis Human Lipids Lipomucopolysaccharidosis Genetic disease Metabolic diseases Niemann Pick disease Tay Sachs disease Cherry red spot Storage disease
Keyword (es)
Lipido Enfermedad hereditaria Metabolismo patologia
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
Metabolic diseases
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
9255709

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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