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20篇 您的检索式:作者名="Labrune P"
    题名 作者 年代 出处 被引量
1Consensus guidelines for manage- ment of glycogen storage disease type 1 b - European Study on Glycogen Storage Disease Type 1 显示文摘Visser G Rake JP Labrune P 2002Eur J Pediatr2002,161,1:1
2Liver glycogen storage diseases dueto phosphorylase system deficiencies:diagnosis thanks to noninvasive blood enzymatic and molecular studies显示文摘Davit-Spraul A Piraud M Dobbelaere D Valayannopoulos V Labrune P Habes D 2011Mol GenetMetab2011,104,12:1
3Common variants in FTO,MC4R,TMEM18,PRL,AIF1,and PCSK1 show evidence of association with adult obesity in the Greek population显示文摘Rouskas K Kouvatsi A Paletas K Papazoglou D Tsapas A Lobbens S Vatin V Durand E Labrune Y Delplanque J Meyre D and Froguel P 0,,02:1
4Glycogen storage disease type 1 and diabetes: learning by comparing and contrasting the two disorders显示文摘Rajas F Labrune P Mithieux G 2013Diabetes Metab2013,39,5:1
5Hepatocellular adenomas in glycogen storage disease type Ⅰ and Ⅲ:a series of 43 patients and review of the literature显示文摘Labrune P Trioche P Duvaltier I 1997J Pediatr Gastroenterol Nutr1997,24,3:1
6Hepatocellular adeno- mas in glycogen storage disease type I and III: a series of 43 pa- tients and review of the literature 显示文摘Labrune P Trioche P Duvaltier I 1997J Pediatr Gastroenterol Nu- tr1997,24,3:1
7Hepatocellular adenomas in glycogen storage disease type I and Ⅲ: a series of 43 patients and review of the literature显示文摘Labrune P Trioche P Duvaltier I 1997J Pediatr Gastroenterol Nutr1997,24,3:1
8Hepatocellular adenoma in glycogen disease type Ⅰ and type Ⅲ:a series of 43 patients and review of literature显示文摘Labrune P Trioche P Duvaltier I 1997J Pediatr Gastroenterol Nutr1997,24,:1
9Hepatocellular adenomas in glycogen storage disease type Ⅰ and Ⅲ:a series of 43 patients and review of the literature显示文摘Labrune P Trioche P Duvaltier I 1997J Pediatr Gastroenterol Nutr1997,24,2:1
10BICOVOX:sintering and grain size dependence of the electrical properties显示文摘Steil M C Fouletier J Labrune P 1999Journal of the European Ceramic Society1999,19,:1
11Hepatocellular adenomas in glycogen storage disease typeⅠ and Ⅲ:a series of 43 patients and review of the literature显示文摘Labrune P Trioche P Duvaltier I 1997J Pediatr Gastroenterol Nutr1997,24,3:1
12Association of a homozygous (TA) 8 pro- moter polymorphism and a N400D mutation of UGT1A1 in a child with Crigler-Najjar type Ⅱ syndrome显示文摘Labrune P Myara A Chalas J Le Bihan B Capel L Franeoual J 2002Hum Mutat2002,20,5:1
13Hepatocellular adenomas in glycogen storage disease type Ⅰ andⅢ:a series of 43 patients and review of the literature显示文摘Labrune P Trioche P Duraltier I 1997J Pediatr Gastroenterol Nutr1997,24,3:1
14Hepatocellular adenonas in glycogen storage disease type Ⅰ and Ⅲ:a series of 43 patients and review of the literature显示文摘Labrune P Trioche P Duvaltier I 1997J Pediatr Gastroenterol Nutr1997,24,2:1
15Cardiomyopathy in glycogen-storage disease type Ⅲ:clinical and echographic study of 18 patients显示文摘LABRUNE P HUGUET P ODIEVRE M 1991Pediatr Cardiol1991,12,:1
16Extensive brain calcifications, leukodystrophy, and formation of parenchymal cysts: a new progressive disorder due to diffuse cerebral microangiopathy 显示文摘Labrune P Lacroix C Goutieres F 1996Neurology1996,46,5:1
17Extensive brain calcifications,leukodystrophy,and formation of parenchymal cysts:a new progressive disorder due to diffuse cerebral microangiopathy显示文摘Labrune P Lacroix C Goutieres F 1996Neurology1996,46,5:1
18Consensus guidelines for management of glycogen storage disease type l b-European Study on Glycogen Storage Disease Type 1 显示文摘Visser G Rake JP Labrune P 2002Eur J Pediatr2002,161,:1
19Guidelines for man- agement of glycogen storage disease type I -European Study on Glycogen Storage Disease Type I (ESGSD I ) 显示文摘Rake JP Visser G Labrune P 2002Eur J Pediatr2002,161,:1
20Fatal liver failure in two children with Niemann Pick disease type B显示文摘Labrune P Bedossa P Huguet P 1991Journal of pediatric gastroenterology and nutrition1991,13,1:1
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