Literature DB >> 14246187

OCULAR HISTOPATHOLOGY IN GENERALIZED GLYCOGENOSIS (POMEPE'S DISEASE).

D TOUSSAINT, P DANIS.   

Abstract

Keywords:  CARBOHYDRATE METABOLISM, INBORN ERRORS; EYE MANIFESTATIONS; GLYCOGENOSIS; GLYCOSIDE HYDROLASES; INFANT; LIVER ENZYMOLOGY; MUSCLES; PATHOLOGY

Mesh：

Substances：

Year:  1965        PMID： 14246187     DOI： 10.1001/archopht.1965.00970030344009

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN： 0003-9950


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  5 in total

1.  Ocular ultrastructural study in a fetus with type II glycogenosis.

Authors:  J Libert; J J Martin; C Ceuterick; P Danis
Journal:  Br J Ophthalmol       Date:  1977-07       Impact factor: 4.638

2.  Pompe's disease: an inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscle.

Authors:  J J Martin; T de Barsy; F van Hoof; G Palladini
Journal:  Acta Neuropathol       Date:  1973-02-19       Impact factor: 17.088

Review 3.  Ocular correlates of inborn metabolic defects.

Authors:  D G Cogan
Journal:  Can Med Assoc J       Date:  1966-11-19       Impact factor: 8.262

4.  [Histochemistry of mucopolysaccharide-like substances (basophilic substances) in skeletal muscle in neuromuscular glycogenosis (type II)].

Authors:  R Schnabel
Journal:  Acta Neuropathol       Date:  1971       Impact factor: 17.088

5.  Temporal neuropathologic and behavioral phenotype of 6neo/6neo Pompe disease mice.

Authors:  Richard L Sidman; Tatyana Taksir; Jonathan Fidler; Michael Zhao; James C Dodge; Marco A Passini; Nina Raben; Beth L Thurberg; Seng H Cheng; Lamya S Shihabuddin
Journal:  J Neuropathol Exp Neurol       Date:  2008-08       Impact factor: 3.685
  5 in total

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