نتایج جستجو برای: lipodystrophy

تعداد نتایج: 5143  

Journal: :Dermatology online journal 2008
Vasco Vieira Serrão Ana Barata Feio

Localized loss of subcutaneous tissue can occur after panniculitis, injections of corticosteroids and other drugs, or associated with infectious, autoimmune or neurologic diseases. The "idiopathic lipoatrophies" are a group of poorly characterized diseases, with focal disappearance of subcutaneous fat, and usually the thighs, abdomen or the ankles are affected. Three subtypes have been describe...

2012
Alison Sleigh Anna Stears Kerrie Thackray Laura Watson Alessandra Gambineri Sath Nag V. Irene Campi Nadia Schoenmakers Soren Brage T. Adrian Carpenter Peter R. Murgatroyd Stephen O'Rahilly Graham J. Kemp David B. Savage

OBJECTIVE Lipid accumulation in skeletal muscle and the liver is strongly implicated in the development of insulin resistance and type 2 diabetes, but the mechanisms underpinning fat accrual in these sites remain incompletely understood. Accumulating evidence of muscle mitochondrial dysfunction in insulin-resistant states has fuelled the notion that primary defects in mitochondrial fat oxidatio...

Journal: :گوارش 0
simin partovi davoud sharifi hamid khalesi

congenital generalized lipodystrophy (cgl) is a rare and progressive disorder (1 in 12 milion). common clinical manifestations are lipoatrophy, acromegaloid feature, acanthosis nigricans, hyperlipidemia, diabetes mellitus or abnormal glucose tolerance test.â rarely fatty liver and cirrhosis is seen. the highest number reported in literature is 8 cases from brazil and 6 cases from scandinavia, r...

Journal: :Current Opinion in Lipidology 2019

Journal: :Surgical & Cosmetic Dermatology 2015

Journal: :Postgraduate Medical Journal 1989

2013
Obaid Ur Rahman Nadeem Khawar Muhammad Aman Khan Jawad Ahmed Kamran Khattak Jumana Yousuf Al-Aama Muhammad Naeem Musharraf Jelani

BACKGROUND Congenital generalized lipodystrophy (CGL) also known as Berardinelli-Seip Congenital Lipodystrophy (BSCL) is a genetically heterogeneous disorder characterized by loss of adipose tissues, Acanthosis nigricans, diabetes mellitus, muscular hypertrophy, hepatomegaly and hypertriglyceridemia. There are four subclinical phenotypes of CGL (CGL1-4) and mutations in four genes AGPAT2, BSCL2...

Journal: :The Journal of Nervous and Mental Disease 1921

Journal: :Indian Journal of Endocrinology and Metabolism 2013

Journal: :Postgraduate Medical Journal 1958

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید