Familial lipodystrophy associated with neurodegeneration and congenital cataracts

Neurology

Volumn 58, Issue 1, 2002, Pages 43-47

  Berger, Joseph R ^a,c   Arioglu Oral, Elif ^b   Taylor, Simeon I ^b  

^a UNIVERSITY OF KENTUCKY   (United States)

^b NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

^c UNIVERSITY OF KENTUCKY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

THYROGLOBULIN; TRANSFERRIN;

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CLINICAL FEATURE; CONGENITAL CATARACT; DIFFERENTIAL DIAGNOSIS; DISEASE ASSOCIATION; DUAL ENERGY X RAY ABSORPTIOMETRY; FAMILIAL DISEASE; FEMALE; GENETIC ANALYSIS; GLYCOSYLATION; HUMAN; INSULIN RESISTANCE; KARYOTYPE; LIPID ANALYSIS; LIPODYSTROPHY; MALE; METABOLIC DISORDER; MULTIPLE SCLEROSIS; MUSCLE BIOPSY; NERVE DEGENERATION; OBESITY; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; SPINOCEREBELLAR DEGENERATION;

EID: 0037039225     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.58.1.43     Document Type: Article

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