Literature DB >> 11298098

A case of congenital generalized lipodystrophy: metabolic effects of four dietary regimens. Lack of association of CGL with polymorphism in the lamin A/C Gene.

R Kazlauskaite, A T Santomauro, J Goldman, K Silver, S Snitker, B A Beamer, C J Yen, A R Shuldiner, B L Wajchenberg.   

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Year:  2001        PMID： 11298098      PMCID： PMC3390933          DOI： 10.1046/j.1365-2265.2001.1216c.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN： 0300-0664            Impact factor:   3.478


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  7 in total

1.  Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy.

Authors:  H Cao; R A Hegele
Journal:  Hum Mol Genet       Date:  2000-01-01       Impact factor: 6.150

2.  Genetic exclusion of 14 candidate genes in lipoatropic diabetes using linkage analysis in 10 consanguineous families.

Authors:  C Vigouroux; E Khallouf; C Bourut; J J Robert; M de Kerdanet; N Tubiana-Rufi; S Fauré; J Weissenbach; J Capeau; J Magré
Journal:  J Clin Endocrinol Metab       Date:  1997-10       Impact factor: 5.958

3.  Molecular scanning of beta-3-adrenergic receptor gene in total congenital lipoatrophic diabetes mellitus.

Authors:  K Silver; J Walston; L Plotnick; S I Taylor; C R Kahn; A R Shuldiner
Journal:  J Clin Endocrinol Metab       Date:  1997-10       Impact factor: 5.958

4.  Human peroxisome proliferator-activated receptor-gamma2: genetic mapping, identification of a variant in the coding sequence, and exclusion as the gene responsible for lipoatrophic diabetes.

Authors:  C Vigouroux; L Fajas; E Khallouf; M Meier; G Gyapay; O Lascols; J Auwerx; J Weissenbach; J Capeau; J Magré
Journal:  Diabetes       Date:  1998-03       Impact factor: 9.461

5.  Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C.

Authors:  R A Speckman; A Garg; F Du; L Bennett; R Veile; E Arioglu; S I Taylor; M Lovett; A M Bowcock
Journal:  Am J Hum Genet       Date:  2000-04       Impact factor: 11.025

6.  Role of lipid oxidation in pathogenesis of insulin resistance of obesity and type II diabetes.

Authors:  J P Felber; E Ferrannini; A Golay; H U Meyer; D Theibaud; B Curchod; E Maeder; E Jequier; R A DeFronzo
Journal:  Diabetes       Date:  1987-11       Impact factor: 9.461

7.  Influence of short-term dexfenfluramine therapy on glucose and lipid metabolism in obese non-diabetic patients.

Authors:  P H Andersen; B Richelsen; J Bak; O Schmitz; N S Sørensen; R Lavielle; O Pedersen
Journal:  Acta Endocrinol (Copenh)       Date:  1993-03
  7 in total
  2 in total

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

Authors:  Mao Fu; Rasa Kazlauskaite; Maria de Fátima Paiva Baracho; Maria Goretti Do Nascimento Santos; José Brandão-Neto; Sandra Villares; Francesco S Celi; Bernardo L Wajchenberg; Alan R Shuldiner
Journal:  J Clin Endocrinol Metab       Date:  2004-06       Impact factor: 5.958

2.  Idiopathic isolated clitoromegaly: A report of two cases.

Authors:  Eray Copcu; Alper Aktas; Nazan Sivrioglu; Ozgen Copcu; Yucel Oztan
Journal:  Reprod Health       Date:  2004-10-04       Impact factor: 3.223
  2 in total

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