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儿童肝糖原累积病1例

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出处 《解放军医学杂志》 CAS CSCD 北大核心 2010年第7期897-898,共2页 Medical Journal of Chinese People's Liberation Army
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  • 1周华,方峰,徐三清,董永绥,李革.儿童代谢性肝沉积病肝组织病理和超微病理特征及其诊断意义[J].中国实用儿科杂志,2007,22(5):370-372. 被引量:10
  • 2John C, Rebeccah L, Michelle G, et al. A complex rearrangement in GBE1 causes both perinatal hypoglycemic collapse and late -juvenile - onset neuromuscular degeneration in glycogen storage disease type Ⅳ of Norwegian forest cats[ J]. Mol Genet Metab,2007,90(4) :383 -392.
  • 3Shin YS. Glycogen storage disease : Clinical, biochemical, and molecular heterogeneity [ J ]. Semin Pediatr Neurol,2006,13 ( 2 ) : 115 - 120.
  • 4Davis MK, Weinstein DA. Liver transplantation in children with glycogen storage disease:Controversies and evaluation of the risk/benefit of this procedure [ J ]. Pediatr Transplant, 2008,12 (2) : 137 - 145.
  • 5Chou JY, Mansfield BC. Mutations in the glucose - 6 - phosphatase - α (G6PC) gene that cause type Ⅰa glycogen storage disease[ J]. Hum Mutat,2008,29(7) :921 -930.
  • 6Sucky FJ, Sokol R J, Balistreri WF. Liver disease in children [ M ]. 2^nd ed. Philadelphia : Lippincott Williams & Wilkins ,2001: 565 -594.
  • 7Zimakas PJ, Rodd CJ. Glycogen storage disease typeⅢ in Inuit children [ J ]. CMAJ,2005,172 ( 3 ) :355 - 358.
  • 8Bernier AV, Sentner CP, Correia CE, et al. Hyperlipidemia in glycogen storage disease type Ⅲ: Effect of age and metabolic control [ J ]. Inherit Metab Dis,2008,31 (6) :729 -732.

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