These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

151 related items for PubMed ID: 6516797

  • 1. Hereditary motor and sensory neuropathy of demyelinating and remyelinating type in children. Ultrastructural and morphometric studies on sural nerve biopsy specimens from ten sporadic cases.
    Nordborg C, Conradi N, Sourander P, Hagberg B, Westerberg B.
    Acta Neuropathol; 1984; 65(1):1-9. PubMed ID: 6516797
    [Abstract] [Full Text] [Related]

  • 2. Autosomal recessive form of hereditary motor and sensory neuropathy type I.
    Gabreëls-Festen AA, Gabreëls FJ, Jennekens FG, Joosten EM, Janssen-van Kempen TW.
    Neurology; 1992 Sep; 42(9):1755-61. PubMed ID: 1513466
    [Abstract] [Full Text] [Related]

  • 3. Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheaths.
    Gabreëls-Festen AA, Joosten EM, Gabreëls FJ, Stegeman DF, Vos AJ, Busch HF.
    Brain; 1990 Dec; 113 ( Pt 6)():1629-43. PubMed ID: 2276038
    [Abstract] [Full Text] [Related]

  • 4. 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; 86(3):279-83. PubMed ID: 7808799
    [Abstract] [Full Text] [Related]

  • 5. [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; 53(3-B):560-9. PubMed ID: 8585811
    [Abstract] [Full Text] [Related]

  • 6. 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; 32(1):91-122. PubMed ID: 864493
    [Abstract] [Full Text] [Related]

  • 7. Clinicopathologic analysis of 124 biopsy-proven peripheral nerve diseases.
    Hong SM, Ha H, Suh JH, Kim KK, Khang SK, Ro JY, Park SH.
    J Korean Med Sci; 2000 Apr; 15(2):211-6. PubMed ID: 10803700
    [Abstract] [Full Text] [Related]

  • 8. [A gait disorder caused by hereditary motor-sensory neuropathy].
    Sauter R.
    Z Orthop Ihre Grenzgeb; 1990 Apr; 128(2):123-7. PubMed ID: 2140641
    [Abstract] [Full Text] [Related]

  • 9. Four novel cases of periaxin-related neuropathy and review of the literature.
    Marchesi C, Milani M, Morbin M, Cesani M, Lauria G, Scaioli V, Piccolo G, Fabrizi GM, Cavallaro T, Taroni F, Pareyson D.
    Neurology; 2010 Nov 16; 75(20):1830-8. PubMed ID: 21079185
    [Abstract] [Full Text] [Related]

  • 10. Minimal pathologic expression of a mutant gene for hereditary motor and sensory neuropathy.
    Dyck PJ, Karnes JL, Windebank AJ, Sparks M, Stevens JC, O'Brien PC.
    Mayo Clin Proc; 1983 Jul 16; 58(7):419-25. PubMed ID: 6865475
    [Abstract] [Full Text] [Related]

  • 11. Neuropathologic and morphometric studies in hereditary motor and sensory neuropathy type II with neurofilament accumulation.
    Goebel HH, Vogel P, Gabriel M.
    Ital J Neurol Sci; 1986 Jun 16; 7(3):325-32. PubMed ID: 3460975
    [Abstract] [Full Text] [Related]

  • 12. Chronic inflammatory demyelinating polyneuropathy or hereditary motor and sensory neuropathy? Diagnostic value of morphological criteria.
    Gabreëls-Festen AA, Gabreëls FJ, Hoogendijk JE, Bolhuis PA, Jongen PJ, Vingerhoets HM.
    Acta Neuropathol; 1993 Jun 16; 86(6):630-5. PubMed ID: 8310819
    [Abstract] [Full Text] [Related]

  • 13. Hypertrophic Charcot-Marie-Tooth disease. Light and electron microscope studies of the sural nerve.
    Low PA, McLeod JG, Prineas JW.
    J Neurol Sci; 1978 Jan 16; 35(1):93-115. PubMed ID: 624962
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood.
    Ouvrier RA, McLeod JG, Conchin TE.
    Brain; 1987 Feb 15; 110 ( Pt 1)():121-48. PubMed ID: 3467805
    [Abstract] [Full Text] [Related]

  • 16. Inflammatory pathological changes in a 2-year-old boy with Charcot-Marie-Tooth disease.
    Nakai Y, Okumura A, Takada H, Negoro T, Watanabe K, Hattori N, Sobue G.
    Brain Dev; 2001 Jul 15; 23(4):258-60. PubMed ID: 11377008
    [Abstract] [Full Text] [Related]

  • 17. [The nosological situation of hereditary motor and sensory neuropathies (HMSN, Charcot-Marie-Tooth disease, neural muscular atrophy)].
    Warzok R, Wattig B, Schwesinger G, Schneeweiss H, Heydenreich F.
    Zentralbl Allg Pathol; 1990 Jul 15; 136(6):549-62. PubMed ID: 2281721
    [Abstract] [Full Text] [Related]

  • 18. Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease.
    Gabreëls-Festen AA, Hoogendijk JE, Meijerink PH, Gabreëls FJ, Bolhuis PA, van Beersum S, Kulkens T, Nelis E, Jennekens FG, de Visser M, van Engelen BG, Van Broeckhoven C, Mariman EC.
    Neurology; 1996 Sep 15; 47(3):761-5. PubMed ID: 8797476
    [Abstract] [Full Text] [Related]

  • 19. Mutations in the MORC2 gene cause axonal Charcot-Marie-Tooth disease.
    Sevilla T, Lupo V, Martínez-Rubio D, Sancho P, Sivera R, Chumillas MJ, García-Romero M, Pascual-Pascual SI, Muelas N, Dopazo J, Vílchez JJ, Palau F, Espinós C.
    Brain; 2016 Jan 15; 139(Pt 1):62-72. PubMed ID: 26497905
    [Abstract] [Full Text] [Related]

  • 20. Hereditary motor and sensory neuropathy--Lom, a novel demyelinating neuropathy associated with deafness in gypsies. Clinical, electrophysiological and nerve biopsy findings.
    Kalaydjieva L, Nikolova A, Turnev I, Petrova J, Hristova A, Ishpekova B, Petkova I, Shmarov A, Stancheva S, Middleton L, Merlini L, Trogu A, Muddle JR, King RH, Thomas PK.
    Brain; 1998 Mar 15; 121 ( Pt 3)():399-408. PubMed ID: 9549516
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.