نتایج جستجو برای: berardinelli

تعداد نتایج: 127  

Journal: :European journal of endocrinology 2010
Jacques Beltrand Najiba Lahlou Tifenn Le Charpentier Guy Sebag Sofia Leka Michel Polak Nadia Tubiana-Rufi Didier Lacombe Marc de Kerdanet Frederic Huet Jean-Jacques Robert Didier Chevenne Pierre Gressens Claire Lévy-Marchal

CONTEXT Recently, in a 4-month proof-of-concept trial, beneficial metabolic effects were reported in non-diabetic children with Berardinelli-Seip congenital lipodystrophy (BSCL); this information prompted us to hypothesize that long-term leptin-replacement therapy might improve or reverse the early complications of the disease in these patients. PATIENTS AND METHODS A 28-month trial was imple...

Journal: :The Journal of clinical endocrinology and metabolism 2003
Anil K Agarwal Vinaya Simha Elif Arioglu Oral Stephanie A Moran Phillip Gorden Stephen O'Rahilly Zohra Zaidi Figen Gurakan Silva A Arslanian Aharon Klar Alyne Ricker Neil H White Lutz Bindl Karen Herbst Kurt Kennel Shailesh B Patel Lihadh Al-Gazali Abhimanyu Garg

Congenital generalized lipodystrophy (CGL) is a rare autosomal recessive disorder characterized by near complete absence of adipose tissue from birth. Recently, mutations in 1-acylglycerol-3-phosphate O-acyltransferase 2 (AGPAT2) and Berardinelli-Seip congenital lipodystrophy 2 (BSCL2) genes were reported in pedigrees linked to chromosomes 9q34 and 11q13, respectively. There are limited data re...

2011
Yuan Tian Junfeng Bi Guanghou Shui Zhonghua Liu Yanhui Xiang Yuan Liu Markus R. Wenk Hongyuan Yang Xun Huang

Obesity is characterized by accumulation of excess body fat, while lipodystrophy is characterized by loss or absence of body fat. Despite their opposite phenotypes, these two conditions both cause ectopic lipid storage in non-adipose tissues, leading to lipotoxicity, which has health-threatening consequences. The exact mechanisms underlying ectopic lipid storage remain elusive. Here we report t...

Journal: :American journal of physiology. Endocrinology and metabolism 2012
Xin Cui Yuhui Wang Lingjun Meng Weihua Fei Jingna Deng Guoheng Xu Xingui Peng Shenghong Ju Ling Zhang George Liu Liping Zhao Hongyuan Yang

Berardinelli-Seip congenital lipodystrophy type 2 (BSCL2) is a recessive disorder characterized by an almost complete loss of adipose tissue, insulin resistance, and fatty liver. BSCL2 is caused by loss-of-function mutations in the BSCL2/seipin gene, which encodes seipin. The essential role for seipin in adipogenesis has recently been established both in vitro and in vivo. However, seipin is hi...

Journal: :Neurology 2011
Jean François Dartigues Catherine Féart

242 Morphometry of dermal nerve fibers in human skin G. Lauria, D. Cazzato, C. Porretta-Serapiglia, J. Casanova-Molla, M. Taiana, P. Penza, R. Lombardi, C.G. Faber, and I.S.J. Merkies 250 Functional changes in Duchenne muscular dystrophy: A 12-month longitudinal cohort study E. Mazzone, G. Vasco, M.P. Sormani, Y. Torrente, A. Berardinelli, S. Messina, A. D’Amico, L. Doglio, L. Politano, F. Cava...

2014
Kenneth Wee Wulin Yang Shigeki Sugii Weiping Han

CGL (Congenital generalized lipodystrophy) is a genetic disorder characterized by near complete loss of adipose tissue along with increased ectopic fat storage in other organs including liver and muscle. Of the four CGL types, BSCL2 (Berardinelli-Seip Congenital lipodystrophy type 2), resulting from mutations in the BSCL2/seipin gene, exhibits the most severe lipodystrophic phenotype with loss ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2007
Kimberly M Szymanski Derk Binns René Bartz Nick V Grishin Wei-Ping Li Anil K Agarwal Abhimanyu Garg Richard G W Anderson Joel M Goodman

Lipodystrophy is a disorder characterized by a loss of adipose tissue often accompanied by severe hypertriglyceridemia, insulin resistance, diabetes, and fatty liver. It can be inherited or acquired. The most severe inherited form is Berardinelli-Seip Congenital Lipodystrophy Type 2, associated with mutations in the BSCL2 gene. BSCL2 encodes seipin, the function of which has been entirely unkno...

Journal: :Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2012
F Schmidt T M Kapellen S Wiegand A Herbst J Wolf E E Fröhlich-Reiterer W Rabl T R Rohrer R W Holl

BACKGROUND Several genetic syndromes are associated with diabetes mellitus (DM). This study aimed to analyse data from the DPV database with regard to frequency, treatment strategies and long-term complications in paediatric DM patients with genetic syndromes, including Turner syndrome (TS), Prader-Willi syndrome (PWS), Friedreich ataxia (FA), Alström syndrome (AS), Klinefelter syndrome (KS), B...

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