Pompe's disease: An inborn lysosomal disorder with storage of glycogen - A study of brain and striated muscle

Acta Neuropathologica

Volumn 23, Issue 3, 1973, Pages 229-244

  Martin, J J ^a,b   de Barsy, Th ^a,b   Van Hoof, F ^a,b   Palladini, G ^a,b,c  

^a UNIVERSITY OF ANTWERP   (Belgium)

^b UNIVERSITÉ CATHOLIQUE DE LOUVAIN   (Belgium)

^c Istituto di Anatomia comparata 'B Grassi' ^*  (Italy)

Author keywords

Basophilic Substance; Glycogen; Glycogen filled Vacuoles; Lysosomes; Pompe's Disease

Indexed keywords

GLUCOSIDASE;

ARTICLE; AUTOPSY; BIOPSY; BRAIN; CYTOCHEMISTRY; ELECTRON MICROSCOPY; GLIA; GLYCOGEN STORAGE DISEASE; HEART DISEASE; HUMAN; INFANT; LYSOSOME; MALE; METABOLISM; MICROSCOPY; MUSCLE; MYENTERIC PLEXUS; PATHOLOGY; SCHWANN CELL; THALAMUS;

AUTOPSY; BIOPSY; BRAIN; GLUCOSIDASES; GLYCOGEN STORAGE DISEASE; HEART DISEASES; HISTOCYTOCHEMISTRY; HUMAN; INFANT; LYSOSOMES; MALE; MICROSCOPY; MICROSCOPY, ELECTRON; MUSCLES; MYENTERIC PLEXUS; NEUROGLIA; SCHWANN CELLS; THALAMUS;

EID: 0015929582     PISSN: 00016322     EISSN: 14320533     Source Type: Journal    
DOI: 10.1007/BF00687878     Document Type: Article

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