Long-term efficacy of leptin replacement in patients with familial partial lipodystrophy, Dunnigan variety (FPLD)

被引：0
|
作者：
Park, Jeany
Javor, Edward D.
Cochran, Elaine K.
Depaoli, Alex M.
Gorden, Phillip
机构：
来源：
DIABETES | 2006年 / 55卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：A18 / A18
页数：1
相关论文
共 50 条
  • [21] Familial partial lipodystrophy, Dunnigan variety - Challenges for patient care during pregnancy: A case report
    Belo S.P.M.
    Magalhães A.C.
    Freitas P.
    Carvalho D.M.
    BMC Research Notes, 8 (1)
  • [22] Phenotypic heterogeneity in patients with familial partial lipodystrophy (Dunnigan variety) related to the site of missense mutations in lamin A/C gene
    Garg, A
    Vinaitheerthan, M
    Weatherall, PT
    Bowcock, AM
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (01): : 59 - 65
  • [23] Localization of the gene for familial partial lipodystrophy (Dunnigan variety) to chromosome 1q21–22
    John M. Peters
    Robert Barnes
    Lynda Bennett
    William M. Gitomer
    Anne M. Bowcock
    Abhimanyu Garg
    Nature Genetics, 1998, 18 : 292 - 295
  • [24] Localization of the gene for familial partial lipodystrophy (Dunnigan variety) to chromosome 1q21-22
    Peters, JM
    Barnes, R
    Bennett, L
    Gitomer, WM
    Bowcock, AM
    Garg, A
    NATURE GENETICS, 1998, 18 (03) : 292 - 295
  • [25] The Metabolic Equivalent BMI in Patients with Familial Partial Lipodystrophy (FPLD) Compared with Those with Severe Obesity
    Koo, Eden
    Foss-Freitas, Maria C.
    Meral, Rasimcan
    Ozer, Muhammet
    Eldin, Abdelwahab J.
    Akinci, Baris
    Miller, Nicole
    Rothberg, Amy E.
    Oral, Elif A.
    OBESITY, 2021, 29 (02) : 274 - 278
  • [26] A Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) with Progeroid Features
    Saha, B.
    Lessel, D.
    Hisama, F. M.
    Leistritz, D. F.
    Friedrich, K.
    Martin, G. M.
    Kubisch, C.
    Oshima, J.
    MOLECULAR SYNDROMOLOGY, 2010, 1 (03) : 127 - 132
  • [27] Dunnigan-type familial partial lipodystrophy (FPLD): a monogenic syndrome of central fat accumulation and insulin resistance due to mutations in nuclear lamin A.
    Hegele, RA
    OBESITY RESEARCH, 2000, 8 : 3S - 3S
  • [28] A case of Dunnigan-type familial partial lipodystrophy (FPLD) due to lamin A/C (LMNA) mutations complicated by end-stage renal disease
    Imachi, Hitomi
    Murao, Koji
    Ohtsuka, Shouji
    Fujiwara, Mako
    Muraoka, Tomie
    Hosokawa, Hitoshi
    Ishida, Toshihiko
    ENDOCRINE, 2009, 35 (01) : 18 - 21
  • [29] A case of Dunnigan-type familial partial lipodystrophy (FPLD) due to lamin A/C (LMNA) mutations complicated by end-stage renal disease
    Hitomi Imachi
    Koji Murao
    Shouji Ohtsuka
    Mako Fujiwara
    Tomie Muraoka
    Hitoshi Hosokawa
    Toshihiko Ishida
    Endocrine, 2009, 35 : 18 - 21
  • [30] Long-term effectiveness and safety of metreleptin in the treatment of patients with partial lipodystrophy
    Oral, Elif A.
    Gorden, Phillip
    Cochran, Elaine
    Araujo-Vilar, David
    Savage, David B.
    Long, Alison
    Fine, Gregory
    Salinardi, Taylor
    Brown, Rebecca J.
    ENDOCRINE, 2019, 64 (03) : 500 - 511
12345