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Journal Abstract Search

171 related items for PubMed ID: 7603395

  • 21. Vincristine treatment revealing asymptomatic hereditary motor sensory neuropathy type 1A.
    Mercuri E, Poulton J, Buck J, Broadbent V, Bamford M, Jungbluth H, Manzur AY, Muntoni F.
    Arch Dis Child; 1999 Nov; 81(5):442-3. PubMed ID: 10519723
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  • 22. Vincristine treatment triggering the expression of asymptomatic Charcot-Marie-Tooth disease.
    Neumann Y, Toren A, Rechavi G, Seifried B, Shoham NG, Mandel M, Kenet G, Sharon N, Sadeh M, Navon R.
    Med Pediatr Oncol; 1996 Apr; 26(4):280-3. PubMed ID: 8600343
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  • 24. Severe vincristine-induced polyneuropathy in a teenager with anaplastic medulloblastoma and undiagnosed Charcot-Marie-Tooth disease.
    Aghajan Y, Yoon JM, Crawford JR.
    BMJ Case Rep; 2017 Apr 24; 2017():. PubMed ID: 28438772
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  • 28. Hypertrophic motor and sensory neuropathy type I (Charcot-Marie-Tooth disease): ultrastructural study of sural nerve biopsy in members of a family.
    Calore EE, Alonso Neto JL, Cavaliere MJ, Perez NM, Russo DH, Wakamatsu A, Maeda MY, Kitamura C.
    Pathologica; 1994 Jun 24; 86(3):279-83. PubMed ID: 7808799
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  • 30. Mild phenotype of Charcot-Marie-Tooth disease type 4B1.
    Murakami T, Kutoku Y, Nishimura H, Hayashi M, Abe A, Hayasaka K, Sunada Y.
    J Neurol Sci; 2013 Nov 15; 334(1-2):176-9. PubMed ID: 23962696
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  • 32. Screening for Charcot-Marie-Tooth type 1A and hereditary neuropathy with liability to pressure palsy in archival nerve biopsy samples by direct-double-differential PCR.
    Beckmann A, Schröder JM.
    Acta Neuropathol; 2000 Nov 15; 100(5):459-63. PubMed ID: 11045666
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  • 33. Charcot-Marie-Tooth (CMT) disease 1A with superimposed inflammatory polyneuropathy in children.
    Desurkar A, Lin JP, Mills K, Al-Sarraj S, Jan W, Jungbluth H, Wraige E.
    Neuropediatrics; 2009 Apr 15; 40(2):85-8. PubMed ID: 19809938
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  • 34. Early onset Charcot-Marie-Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2-related neuropathy.
    Tufano M, Cappuccio G, Terrone G, Manganelli F, Pisciotta C, Geroldi A, Capponi S, Del Giudice E.
    J Peripher Nerv Syst; 2015 Dec 15; 20(4):415-8. PubMed ID: 26307494
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  • 35. [From gene to disease; Charcot-Marie-Tooth disease or the hereditary motor and sensory neuropathies].
    Verhamme C, Baas F.
    Ned Tijdschr Geneeskd; 2005 Jul 02; 149(27):1505-9. PubMed ID: 16032995
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  • 37. Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review.
    Berciano J, García A, Gallardo E, Peeters K, Pelayo-Negro AL, Álvarez-Paradelo S, Gazulla J, Martínez-Tames M, Infante J, Jordanova A.
    J Neurol; 2017 Aug 02; 264(8):1655-1677. PubMed ID: 28364294
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  • 38. X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic study.
    Birouk N, LeGuern E, Maisonobe T, Rouger H, Gouider R, Tardieu S, Gugenheim M, Routon MC, Léger JM, Agid Y, Brice A, Bouche P.
    Neurology; 1998 Apr 02; 50(4):1074-82. PubMed ID: 9566397
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