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线粒体肌病伴脂质沉积1例报道及文献复习 被引量:2

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出处 《实用神经疾病杂志》 2005年第4期99-100,共2页
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参考文献9

  • 1Luft R, Ikkos D, Palmieri G, et al. A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study. J Clin Invest,1962 ,41:1776~1804.
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  • 3Campos Y,Huertas R,Bautista J,et al. Muscle carnitine deficiency and lipid storage myopathy in pathients with mitochondrial myopathy. Muscle &Nerve,1993,16:778~781.
  • 4Dalakas MC,Leon-Monzon ME,Bernardini Isa, et al. Zidovodine induced mitochondrial myopathy is associated with muscle carnitine deficiency and lipid storage. Ann Neurol,1994,35:482~487.
  • 5Turnbull DM,Shepherd IM,Ashworth B,et al. Lipid storage myopathy associated with low acyl-CoA dehydrogenase activites. Brain,1988,111:815~828.
  • 6陈琳,郭玉璞,任海涛,赵燕环.线粒体肌病伴脂质沉积[J].脑与神经疾病杂志,2002,10(3):142-145. 被引量:9
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二级参考文献12

  • 1[1]Campos Y. Huertas R,Bautista J, et al. Muscle carnitine deficiency and lipid storage myopathy in pathients with mitochondrial myopathy. Muscle & Nerve, 1993,16∶778~781.
  • 2[2]Garavaglia B, Uziel G, Dworzak F, et al. Primary carnitine deficiency. Heterozygote and intrafamilial phenotypic variation. Neuroloy, 1991,41∶1691~1693.
  • 3[3]Dalakas MC, Leon-Monzon ME, Bernardini Isa, et al. Zidovudineinduced mitochondrial myopathy is associated with muscle carnitine deficiency and lipid storage. Ann Neurol, 1994,35∶482~487.
  • 4[4]Turnbull DM, Shepherd IM, Ashworth B, et al. Lipid storage myopathy associated with low acyl-CoA dehydrogenase activites. Brain, 1988,111∶815~828.
  • 5[5]Patten BM, Shabot JM, Alperin J, et al. Hepatitis-associated lipid storage myopathy. Ann Intern Med, 1977,87∶471~421.
  • 6[6]Arenas J, Gonzalez-Crespo MR, Campos Y, et al. Abnormal carnitine ditribution in the muscles of patients with idiopathic inflammatory myopathy. Arthritis & Rheumatism, 1996,39∶1869~1874.
  • 7[7]Antozzi C, Garavaglia B, Mora M, et al. Late-onset riboflavin-responsive myopathy with combined multiple acyl conenzyme A dehydrogenase and respiratory chain deficiency. Neurology, 1994,44∶2153~2158.
  • 8[8]Araki E, Kobayashi T, Kohtake N, et al. Ariboflavin-responsive lipid storage myopathy due to multiple acyl-CoA dehydrogenase deficiency: an adult case. Journal of the neurological sciences, 1994,126∶202~205.
  • 9[9]DiDonato S, Gellera C, Peluchetti D, et al. Normalization of short-chain acylcoenzyme A dehydrogenase after riboflavin treatment in girl with multiple acycoenzyme A dehydrogenase-deficient myopathy. Ann Neurol, 1989,25∶479~484.
  • 10[10]Vergani L, Barile M, Angelini C, et al. Riboflavin therapy: biochemical heterogeneity in tow adult lipid storage myopathies. Brain, 1999,122∶2401~2411.

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二级引证文献7

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