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多轴空病患者一例临床和病理特征分析 被引量:1

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出处 《中华神经科杂志》 CAS CSCD 北大核心 2006年第3期202-203,共2页 Chinese Journal of Neurology
基金 国家自然科学基金资助项目(30370510) 博士学科点专项科研基金资助项目(20030558058) 中国博士后科学基金资助项目(2005037172)
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参考文献4

  • 1Engel AG,Gomez MR.Congenital myopathy associated with multisegmental degeneration of the muscle fibres.Trans Am Neurol Assoc,1966,91:222-223.
  • 2Engel AG,Gomez MR,Groover RV.Multicore disease.A recently recognized congenital myopathy associated with multifocal degeneration of muscle fibers.Mayo Clin Proc,1971,46:666-681.
  • 3Fardeau M,Tome FMS.Congenital myopathies.In:Engel AG,Franzini-Armstrong C,eds.Myology.2nd ed.New York:McGraw-Hill,1994.1505-1507.
  • 4Vallat JM,de Lumley L,Loubet A,et al.Coexistence of minicores,cores,and rods in the same muscle biopsy.A new example of mixed congenital myopathy.Acta Neuropathol (Berl),1982,58:229-232.

同被引文献14

  • 1Engel AG,Gomez MR. Congenital myopathy associated with multisegmental degeneration of the muscle fibres[J].Transactions of the American Neurological Association,1966.222-223.
  • 2Jungbluth H,Sewry CA,Muntoni F. Core myopathies[J].Seminars in Pediatric Neurology,2011.239-249.
  • 3Sharma MC,Gulati S,Sarkar C. Multi-minicore disease:A rare form of myopathy[J].Neurology India,2007.50-53.
  • 4Jungbluth H,Sewry C,Brown SC. Minicore myopathy in children:a clinical and histopathological study of 19 cases[J].Neuromuscular Disorders,2000.264-273.
  • 5Ferreiro A,Estournet B,Chateau D. Multi-minicore disease searching for boundaries:phenotype analysis of 38 cases[J].Annals of Neurology,2000.745-757.
  • 6Nadaj-Pakleza A,Fidzia(n)ska A,Ryniewicz B. Multi-minicore myopathy:a clinical and histopath-ological study of 17 cases[J].Folia Neuropathologica,2007.56-65.
  • 7Sriram KB,Thornton A,Antic R. Spontaneous mode noninvasive ventilation fails to treat respiratory failure in a patient with Multi-mincore disease:a case report[J].Cases J,2008.93.
  • 8Vijayakanthi N,Saha A,Dubey NK. Multiminicore disease with respiratory failure[J].Pediatric Neurology,2011.295-298.
  • 9Treves S,Jungbluth H,Muntoni F. Congenital muscle disorders with cores:the ryanodine receptor calcium channel paradigm[J].Current Opinion in Pharmacology,2008.319-326.
  • 10Pandey R,Chandratre S,Roberts A. Central core myopathy with RYR1 mutation masks 5q spinal muscular atrophy[J].European Journal of Neurology,2011.70-73.

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