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Literature DB >> 14427628

Tay-Sachs' disease with visceral involvement and its relationship to Niemann-Pick's disease.

R M NORMAN, H URICH, A H TINGEY, R A GOODBODY.

Abstract

Entities: Disease

Keywords: AMAUROTIC FAMILY IDIOCY/pathology; LIPOIDOSIS/pathology

Mesh：

Year: 1959 PMID： 14427628 DOI： 10.1002/path.1700780208

Source DB: PubMed Journal: J Pathol Bacteriol ISSN： 0368-3494

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Cited

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20 in total

1. TAY-SACHS DISEASE WITH VISCERAL INVOLVEMENT AND ITS RELATION TO GARGOYLISM.

Authors: R M NORMAN; A H TINGEY; C G NEWMAN; S P WARD
Journal: Arch Dis Child Date: 1964-12 Impact factor: 3.791

2. A case of juvenile Gaucher's disease with intraneuronal lipid storage.

Authors: A F MALONEY; J N CUMINGS
Journal: J Neurol Neurosurg Psychiatry Date: 1960-08 Impact factor: 10.154

3. GM1-generalized gangliosidosis variant with cardiomegaly.

Authors: P F Benson; A Barbarik; S P Brown; T P Mann
Journal: Postgrad Med J Date: 1976-03 Impact factor: 2.401

4. Lymphocyte inclusions in the juvenile type of generalized ceroid-lipofuscinosis. An electron microscopic study.

Authors: G Schwendemann
Journal: Acta Neuropathol Date: 1976-12-21 Impact factor: 17.088

Review 5. Progress in investigations of sphingolipidoses.

Authors: M Adachi; L Schneck; B W Volk
Journal: Acta Neuropathol Date: 1978-08-07 Impact factor: 17.088

6. The skeletal phenotype of intermediate GM1 gangliosidosis: Clinical, radiographic and densitometric features, and implications for clinical monitoring and intervention.

Authors: Carlos R Ferreira; Debra S Regier; Robin Yoon; Kristen S Pan; Jean M Johnston; Sandra Yang; Jürgen W Spranger; Cynthia J Tifft
Journal: Bone Date: 2019-11-06 Impact factor: 4.398

Tay-Sachs' disease with visceral involvement and its relationship to Niemann-Pick's disease.

1. TAY-SACHS DISEASE WITH VISCERAL INVOLVEMENT AND ITS RELATION TO GARGOYLISM.

2. A case of juvenile Gaucher's disease with intraneuronal lipid storage.

3. GM1-generalized gangliosidosis variant with cardiomegaly.

4. Lymphocyte inclusions in the juvenile type of generalized ceroid-lipofuscinosis. An electron microscopic study.

Review 5. Progress in investigations of sphingolipidoses.

6. The skeletal phenotype of intermediate GM1 gangliosidosis: Clinical, radiographic and densitometric features, and implications for clinical monitoring and intervention.

7. Chemical studies in gargoylism.

8. The liver in lipidosis. An electron miscroscopic and histochemical study.

9. Niemann-Pick disease type C. Study on the nature of the cerebral storage process.

10. Corneal clouding in GM1-generalized gangliosidosis.