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Journal Abstract Search

141 related items for PubMed ID: 7421358

  • 21. [Electron microscopic studies of the sural nerve in a typical Charcot-Marie-Tooth disease].
    Mizutani T, Furukawa T.
    Rinsho Shinkeigaku; 1976 Jun; 16(6):451-6. PubMed ID: 986283
    [No Abstract] [Full Text] [Related]

  • 22. Hypertrophic nerve roots in a case of Roussy-Lévy syndrome.
    Haubrich C, Krings T, Senderek J, Züchner S, Schröder JM, Noth J, Töpper R.
    Neuroradiology; 2002 Nov; 44(11):933-7. PubMed ID: 12428130
    [Abstract] [Full Text] [Related]

  • 23. [Renaut's bodies and familial neuropathy of the Dejerine-Sottas type. Apropos of 2 anatomo-clinical cases].
    Pasquier B, Couderc P, Pasquier D.
    Sem Hop; 2002 Nov; 51(31-34):2103-7. PubMed ID: 52195
    [Abstract] [Full Text] [Related]

  • 24. Charcot-Marie-Tooth disease with sensorineural hearing loss--an autosomal dominant trait.
    Kousseff BG, Hadro TA, Treiber DL, Wollner T, Morris C.
    Birth Defects Orig Artic Ser; 1982 Nov; 18(3B):223-8. PubMed ID: 7139106
    [No Abstract] [Full Text] [Related]

  • 25. [Autopsy case of Charcot-Marie-Tooth disease with optic nerve atrophy and degeneration of the spinal tract. A family with muscular atrophy, ataxia, retinal degeneration and diabetes mellitus].
    Oguchi K, Tsubaki T, Ikuta F.
    Rinsho Shinkeigaku; 1977 Jan; 17(1):52-7. PubMed ID: 557401
    [No Abstract] [Full Text] [Related]

  • 26. Peripheral nerve extracellular matrix remodeling in Charcot-Marie-Tooth type I disease.
    Palumbo C, Massa R, Panico MB, Di Muzio A, Sinibaldi P, Bernardi G, Modesti A.
    Acta Neuropathol; 2002 Sep; 104(3):287-96. PubMed ID: 12172915
    [Abstract] [Full Text] [Related]

  • 27. [Delerium patterns in Déjerine-Sottas disease].
    Barcia D, Muñóz R.
    Actas Luso Esp Neurol Psiquiatr Cienc Afines; 1980 Sep; 8(5):337-46. PubMed ID: 7457222
    [No Abstract] [Full Text] [Related]

  • 28. [Contribution of morphological studies of the peripheral nerve to a better comprehension of Charcot-Marie-Tooth atrophy and Roussy-Levy hereditary areflexic dystaxia].
    Lapresle J.
    Acquis Med Recent; 1980 Sep; ():91-6. PubMed ID: 7395444
    [No Abstract] [Full Text] [Related]

  • 29. Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X.
    Kleopa KA, Zamba-Papanicolaou E, Alevra X, Nicolaou P, Georgiou DM, Hadjisavvas A, Kyriakides T, Christodoulou K.
    Neurology; 2006 Feb 14; 66(3):396-402. PubMed ID: 16476939
    [Abstract] [Full Text] [Related]

  • 30. [Hypertrophic polyneuropathy].
    Nyberg-Hansen R.
    Tidsskr Nor Laegeforen; 1974 Aug 10; 94(21-22):1302-5. PubMed ID: 4409748
    [No Abstract] [Full Text] [Related]

  • 31. The peroneal muscular atrophy syndrome. Clinical, genetic, electrophysiological and nerve biopsy studies. Part 2. Observations on pathological changes in sural nerve biopsies.
    Madrid R, Bradley WG, Davis CJ.
    J Neurol Sci; 1977 May 10; 32(1):91-122. PubMed ID: 864493
    [Abstract] [Full Text] [Related]

  • 32. Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations.
    Sivakumar K, Kyriakides T, Puls I, Nicholson GA, Funalot B, Antonellis A, Sambuughin N, Christodoulou K, Beggs JL, Zamba-Papanicolaou E, Ionasescu V, Dalakas MC, Green ED, Fischbeck KH, Goldfarb LG.
    Brain; 2005 Oct 10; 128(Pt 10):2304-14. PubMed ID: 16014653
    [Abstract] [Full Text] [Related]

  • 33. A brief review of inherited hypertrophic neuropathy.
    Dyck PJ.
    Birth Defects Orig Artic Ser; 1971 Feb 10; 7(2):66-71. PubMed ID: 4950914
    [No Abstract] [Full Text] [Related]

  • 34. Clinical, electrophysiological and molecular genetic studies in a family with X-linked dominant Charcot-Marie-Tooth neuropathy presenting a novel mutation in GJB1 Promoter and a rare polymorphism in LITAF/SIMPLE.
    Beauvais K, Furby A, Latour P.
    Neuromuscul Disord; 2006 Jan 10; 16(1):14-8. PubMed ID: 16373087
    [Abstract] [Full Text] [Related]

  • 35. [Familial fibula amyotrophies of neurogenic origin].
    Vallat JM, Vital C.
    Cah Med; 1971 Jun 30; 12(10):803-15. PubMed ID: 4107838
    [No Abstract] [Full Text] [Related]

  • 36. [Charcot-Marie-Tooth disease. Study of sural nerve biopsy in 41 patients].
    Freitas MR, Nascimento OJ, Chimelli L, de Freitas GR.
    Arq Neuropsiquiatr; 1995 Sep 30; 53(3-B):560-9. PubMed ID: 8585811
    [Abstract] [Full Text] [Related]

  • 37. [Peroneal atrophy in Tunisia. Study of 70 cases, pure or associated with other heredodegenerative diseases].
    Ben Hamida M, Letaief F, Ben Hamida C, Samoud S.
    J Neurol Sci; 1981 Jun 30; 50(3):335-56. PubMed ID: 7264702
    [Abstract] [Full Text] [Related]

  • 38. Malignant melanoma and Charcot-Marie-Tooth disease.
    Greene MH, Mead GD, Reimer RR, Bergfeld WF, Fraumeni JF.
    Am J Med Genet; 1980 Jun 30; 5(1):69-71. PubMed ID: 7395902
    [Abstract] [Full Text] [Related]

  • 39. [Report of 9 cases of hereditary neuromuscular atrophy and investigation of its genetic patterns].
    Li ZX.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1983 Aug 30; 16(4):210-2. PubMed ID: 6641396
    [No Abstract] [Full Text] [Related]

  • 40. Hypertrophic form of peroneal muscular atrophy (PMA): unusual nerve conduction results.
    Streib EW, Sun SF, Kimberling W, Smith SA.
    Muscle Nerve; 1984 Jan 30; 7(1):32-4. PubMed ID: 6700627
    [Abstract] [Full Text] [Related]

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