Literature DB >> 4933543

Generalized lipodystrophy.

M Seip.   

Abstract

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Year:  1971        PMID: 4933543     DOI: 10.1007/978-3-642-65213-4_2

Source DB:  PubMed          Journal:  Ergeb Inn Med Kinderheilkd        ISSN: 0071-111X


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  8 in total

1.  Membranoproliferative glomerulonephritis with partial lipodystrophy: discordant occurrence in identical twins.

Authors:  W Reichel; J Köbberling; H Fischbach; F Scheler
Journal:  Klin Wochenschr       Date:  1976-01-15

2.  Congenital total lipodystrophy and peripheral pulmonary artery stenosis.

Authors:  O Uzun; M E Blackburn; J L Gibbs
Journal:  Arch Dis Child       Date:  1997-05       Impact factor: 3.791

Review 3.  Lipoatrophic diabetes.

Authors:  H Dörfler; G Rauh; R Bassermann
Journal:  Clin Investig       Date:  1993-04

4.  Lipodystrophy of the extremities. A dominantly inherited syndrome associated with lipatrophic diabetes.

Authors:  J Köbberling; B Willms; R Kattermann; W Creutzfeldt
Journal:  Humangenetik       Date:  1975-09-10

5.  The Wiedemann-Rautenstrauch or neonatal progeroid syndrome. Report of a patient with consanguineous parents.

Authors:  E A Devos; J G Leroy; J P Frijns; H Van den Berghe
Journal:  Eur J Pediatr       Date:  1981-07       Impact factor: 3.183

6.  Computed tomography findings of congenital generalized lipodystrophy: multiple nodular fatty liver and diffuse sclerosis of bones.

Authors:  Takayoshi Shinya; Shuhei Sato; Shiro Akaki; Takeshi Ogata; Katsuya Kato; Atsuhito Tone; Susumu Kanazawa
Journal:  Radiat Med       Date:  2007-11-26

7.  Hepatic ultrastructure in leprechaunism. Hepatic ultrastructural evidence suggesting a syndrome with defective hepatic glucose release.

Authors:  S I Roth; H K Schedewie; D M Bier; H H Conaway; J Olefsky; A Rubenstein; M J Elders
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1982

8.  Identification of a novel nonsense mutation and a missense substitution in the AGPAT2 gene causing congenital generalized lipodystrophy type 1.

Authors:  Amirreza Haghighi; Maryam Razzaghy-Azar; Ali Talea; Mahnaz Sadeghian; Sian Ellard; Alireza Haghighi
Journal:  Eur J Med Genet       Date:  2012-08-01       Impact factor: 2.708

  8 in total

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