GANGLIOSIDOSIS WITH TOTAL HEXOSAMINIDASE DEFICIENCY: CLINICAL, BIOCHEMICAL AND ULTRASTRUCTURAL STUDIES AND COMPARISON WITH CONVENTIONAL CASES OF TAY-SACHS DISEASE
- Other title
- GANGLIOSIDOSE AVEC UN DEFICIT TOTAL EN HEXOSAMINIDASE: ETUDES CLINIQUE, BIOCHIMIQUE ET ULTRASTRUCTURALE ET COMPARAISON AVEC DES CAS CONVENTIONNELS DE MALADIE DE TAY-SACHS (fr)
- Author
- FONTAINE G; RESIBOIS A; TONDEUR M; JONNIAUX G; FARRIAUX JP; VOET W; MAILLARD E; LOEB H
DEP. PEDIATR., UNIV. LILLE, FR. - Source
- ACTA NEUROPATHOL.; ALLEM.; DA. 1973; VOL. 23; NO 2; PP. 118-132; BIBL. 2P.
- Document type
- Serial Issue
- Language
- English
- Keyword (fr)
- IDIOTIE AMAUROTIQUE FAMILIALE INFANTILE GANGLIOSIDOSEGM2 SANDHOFF SPHINGOLIPIDOSE HEREDITAIRE DEFICIT HEREDITAIRE ENZYME HEXOSAMINIDASE ANATOMOPATHOLOGIE ENCEPHALE ANATOMOPATHOLOGIE FOIE HISTOCHIMIE GANGLIOSIDOSE GM2 SANDHOFF CYTOPATHOLOGIE FOIE ENCEPHALE ENFANT MALADIES METABOLIQUES
- Keyword (en)
- METABOLIC DISEASES
- Keyword (es)
- ENFERMEDADES METABOLICAS
- Classification
- Discipline
- Endocrinopathies
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- PASCAL733623331
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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