Clinical and laboratory data of a large series of patients with congenital generalized lipodystrophy. - Wikidata - awgldk - TriplyDB

Clinical and laboratory data of a large series of patients with congenital generalized lipodystrophy.

Clinical and laboratory data of a large series of patients with congenital generalized lipodystrophy.

http://www.wikidata.org/entity/Q31059435

about

Normal bone density and trabecular bone score, but high serum sclerostin in congenital generalized lipodystrophy.High prevalence of Berardinelli-Seip Congenital Lipodystrophy in Rio Grande do Norte State, Northeast Brazil.Seipin deficiency leads to defective parturition in mice.Early commitment of cardiovascular autonomic modulation in Brazilian patients with congenital generalized lipodystrophy.Nurses' knowledge about Berardinelli-Seip Congenital Lipodystrophy.Causes of death in patients with Berardinelli-Seip congenital generalized lipodystrophy.Exploring Seipin: From Biochemistry to Bioinformatics Predictions Impairment of respiratory muscle strength in Berardinelli-Seip congenital lipodystrophy subjects

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Clinical and laboratory data of a large series of patients with congenital generalized lipodystrophy.

http://www.wikidata.org/entity/Q31059435

description

2016 nî lūn-bûn

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2016 թուականի Մարտին հրատարակուած գիտական յօդուած

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2016 թվականի մարտին հրատարակված գիտական հոդված

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2016年の論文

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Diabetology and Metabolic Syndrome

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Clinical and laboratory data o ...... tal generalized lipodystrophy.

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Lucia Helena C Nobrega

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Maria F P Baracho

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Maria Goretti do Nascimento Santos

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Natalia Nobrega de Lima

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Selma Maria Bezerra Jeronimo

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P2860

Seipin deficiency alters fatty acid Delta9 desaturation and lipid droplet formation in Berardinelli-Seip congenital lipodystrophy

Mutations in Gng3lg and AGPAT2 in Berardinelli-Seip congenital lipodystrophy and Brunzell syndrome: phenotype variability suggests important modifier effects

Homeostasis model assessment: insulin resistance and ?-cell function from fasting plasma glucose and insulin concentrations in man

Evolution in health and medicine Sackler colloquium: Consanguinity, human evolution, and complex diseases

Standards of medical care in diabetes--2013

The natural history of insulin secretory dysfunction and insulin resistance in the pathogenesis of type 2 diabetes mellitus.

Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.

AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34.

An undiagnosed endocrinometabolic syndrome: report of 2 cases.

Phenotypic heterogeneity in body fat distribution in patients with congenital generalized lipodystrophy caused by mutations in the AGPAT2 or seipin genes.

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Josivan Gomes Lima

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