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Journal Abstract Search

157 related items for PubMed ID: 1513466

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  • 5. A cohort study of Han Chinese MFN2-related Charcot-Marie-Tooth 2A.
    Lv H, Wang L, Zhang W, Wang Z, Zuo Y, Liu J, Yuan Y.
    J Neurol Sci; 2015 Nov 15; 358(1-2):153-7. PubMed ID: 26382835
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  • 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
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  • 11. 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
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  • 12. [A gait disorder caused by hereditary motor-sensory neuropathy].
    Sauter R.
    Z Orthop Ihre Grenzgeb; 1990 Jul 16; 128(2):123-7. PubMed ID: 2140641
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  • 13. 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 16; 110 ( Pt 1)():121-48. PubMed ID: 3467805
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  • 14. Intermediate nerve conduction velocities define X-linked Charcot-Marie-Tooth neuropathy families.
    Nicholson G, Nash J.
    Neurology; 1993 Dec 16; 43(12):2558-64. PubMed ID: 8255457
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  • 15. Nerve and muscle biopsy in a case of hereditary motor and sensory neuropathy type III with basal lamina onion bulbs.
    Bornemann A, Hansen FJ, Schmalbruch H.
    Neuropathol Appl Neurobiol; 1996 Feb 16; 22(1):77-81. PubMed ID: 8866786
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  • 16. Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I).
    Gabreëls-Festen AA, Joosten EM, Gabreëls FJ, Jennekens FG, Janssen-van Kempen TW.
    J Neurol Sci; 1992 Feb 16; 107(2):145-54. PubMed ID: 1564512
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  • 17. 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
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  • 18. [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 Jan 16; 136(6):549-62. PubMed ID: 2281721
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  • 19. Genotype-phenotype correlations in Charcot-Marie-Tooth disease type 2 caused by mitofusin 2 mutations.
    Calvo J, Funalot B, Ouvrier RA, Lazaro L, Toutain A, De Mas P, Bouche P, Gilbert-Dussardier B, Arne-Bes MC, Carrière JP, Journel H, Minot-Myhie MC, Guillou C, Ghorab K, Magy L, Sturtz F, Vallat JM, Magdelaine C.
    Arch Neurol; 2009 Dec 16; 66(12):1511-6. PubMed ID: 20008656
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  • 20. [A family of hereditary motor and sensory neuropathy type I with a new type of myelin P0 mutation].
    Ohnishi A, Ohnari K, Hashimoto T, Hayasaka K, Yoshimura T, Fukushima Y.
    Rinsho Shinkeigaku; 1994 Jun 16; 34(6):546-51. PubMed ID: 7525134
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