Lipoid Proteinosis: In Vivo and in Vitro Evidence for a Lysosomal Storage Disease

Author:

Bauer Eugene A.,Santa-Cruz Daniel J.,Eisen Arthur Z.

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference25 articles.

1. Urbach-Wiethe disease (lipoglycoproteinosis; lipoid proteinosis; hyalinosis cutis et mucosae). A review;Hofer;Acta Dermatovenerol (Stockh),1973

2. Lipoid proteinosis;Gordon;Birth Defects,1971

3. Lipoid proteinosis;Caro;Int J Dermatol,1978

4. Visceral involvement in lipoid proteinosis;Caplan;Arch Dermatol,1967

5. Study of the lipids in the skin lesions in Urbach-Wiethe disease;Aznar;Clin Chim Acta,1977

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1. Metabolomics in Lipoid Proteinosis;Current Metabolomics and Systems Biology;2020-09-06

2. Pathobiology of Christianson syndrome: Linking disrupted endosomal-lysosomal function with intellectual disability and sensory impairments;Neurobiology of Learning and Memory;2019-11

3. Vesiculobullous eruption revealing lipoid proteinosis: A potential diagnostic pitfall. A case report and a brief review;International Journal of Pediatrics and Adolescent Medicine;2015-09

4. Degenerative and metabolic diseases;McKee's Pathology of the Skin;2012

5. 14 Cutaneous deposits;Weedon's Skin Pathology;2010

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