ライフサイエンスコーパス: partial lipodystrophy

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1 We describe a family with MPGN and acquired partial lipodystrophy.

2 utaneous fat have a phenotype reminiscent of partial lipodystrophy.

3 odystrophy, or later in life, as in familial partial lipodystrophy.

4 C has been reported in patients with MAD and partial lipodystrophy.

5 zed lipodystrophy (8 patients) or Dunnigan's partial lipodystrophy (2 patients) were included in this

6 gene (encoding lamin A/C) underlie familial partial lipodystrophy, a syndrome of monogenic insulin r

7 ntial splice site mutation in a proband with partial lipodystrophy and a history of childhood yolk sa

8 ty liver dystrophy (fld) mice, which exhibit partial lipodystrophy and have diminished peripheral adi

9 ociated with adverse side effects, including partial lipodystrophy and metabolic syndrome.

10 - a disorder characterized by short stature, partial lipodystrophy, and insulin resistance.

11 ncluding muscular dystrophy, cardiomyopathy, partial lipodystrophy, and progeroid syndromes.

12 rticular muscular dystrophy, cardiomyopathy, partial lipodystrophy, and progeroid syndromes.

13 bited a reduction in body weight and length, partial lipodystrophy, and systemic insulin resistance.

14 lear LMNA cause laminopathies, which include partial lipodystrophies associated with metabolic syndro

15 bjects; 2) describe a stereotyped pattern of partial lipodystrophy associated with all the features o

16 ism and estimating the pathogenesis of human partial lipodystrophy caused by CIDEC mutations.

17 in patients with a novel subtype of familial partial lipodystrophy, designated as FPLD4.

18 Familial partial lipodystrophy, Dunnigan variety, (FPLD, OMIM 308

19 Familial partial lipodystrophy (FPLD), Dunnigan variety, is an au

20 olve muscle defects, and the other, familial partial lipodystrophy (FPLD), involves loss of subcutane

21 udes residues genetically linked to familial partial lipodystrophy (FPLD).

22 uscular dystrophy and Dunnigan-type familial partial lipodystrophy (FPLD).

23 ith forms of muscular dystrophy and familial partial lipodystrophy (FPLD).

24 The apparent partial lipodystrophy in Reep1 null mice, although less

25 or was shown in family members with acquired partial lipodystrophy, it did not segregate with the ren

26 Partial lipodystrophy (PLD; MIM 151660) is an inherited

27 egregated with a similar phenotype including partial lipodystrophy, severe insulin resistance and typ

28 we show a polygenic contribution to familial partial lipodystrophy type 1, a severe form of insulin r

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