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Journal Abstract Search

156 related items for PubMed ID: 18957892

  • 21. A novel MPZ gene mutation in congenital neuropathy with hypomyelination.
    Kochanski A, Drac H, Kabzińska D, Ryniewicz B, Rowińska-Marcińska K, Nowakowski A, Hausmanowa-Petrusewicz I.
    Neurology; 2004 Jun 08; 62(11):2122-3. PubMed ID: 15184631
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  • 23. Expression of mitofusin 2(R94Q) in a transgenic mouse leads to Charcot-Marie-Tooth neuropathy type 2A.
    Cartoni R, Arnaud E, Médard JJ, Poirot O, Courvoisier DS, Chrast R, Martinou JC.
    Brain; 2010 May 08; 133(Pt 5):1460-9. PubMed ID: 20418531
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  • 24. [Congenital hereditary motor and sensory neuropathy].
    Routon MC, Robain O, Mayer M, Jardin L, Ponsot G.
    Rev Neurol (Paris); 1991 May 08; 147(8-9):577-85. PubMed ID: 1962067
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  • 26. Hereditary motor and sensory neuropathy with optic atrophy. Ultrastructural and morphometric observations on nerve fibers, mitochondria, and dense-cored vesicles.
    Sommer C, Schröder JM.
    Arch Neurol; 1989 Sep 08; 46(9):973-7. PubMed ID: 2775013
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  • 28. [Giant axonal neuropathy. Presentation of 2 familial cases].
    Maraví Petri E, García-Bragado F, Martín Ruiz E, Guarch R, Ruiz de Azúa Y, Yoldi ME.
    Neurologia; 1989 Sep 08; 4(1):24-30. PubMed ID: 2698683
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  • 30. Complexity of the Hereditary Motor and Sensory Neuropathies: Clinical and Cellular Characterization of the MPZ p.D90E Mutation.
    Lupo V, Pascual-Pascual SI, Sancho P, Calpena E, Gutiérrez-Molina M, Mateo-Martínez G, Espinós C, Arriola-Pereda G.
    J Child Neurol; 2015 Oct 08; 30(11):1544-8. PubMed ID: 25694466
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  • 31. [A family of hereditary motor and sensory neuropathy with spastic paraplegia (HMSN type V)].
    Murayama T, Nagamatsu M, Sugimura K, Matsuoka Y, Takahashi A.
    Rinsho Shinkeigaku; 1989 Oct 08; 29(10):1272-7. PubMed ID: 2691166
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  • 32. Giant axonal neuropathy in a child with insulin-dependent diabetes mellitus.
    Hoffman WH, Carroll JE, Perry GY, Hartlage PL, Kaminer SJ, Flowers NC, Oh SJ, Kelly DR.
    J Child Neurol; 1995 May 08; 10(3):250-3. PubMed ID: 7642902
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  • 35. Autosomal-recessive and X-linked forms of hereditary motor and sensory neuropathy in childhood.
    Ouvrier R, Geevasingha N, Ryan MM.
    Muscle Nerve; 2007 Aug 08; 36(2):131-43. PubMed ID: 17410579
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  • 36. [Molecular mechanisms of hereditary neuropathy: genotype-phenotype correlation].
    Nakagawa M, Takashima H.
    Rinsho Byori; 2003 Jun 08; 51(6):536-43. PubMed ID: 12884740
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  • 37. Infantile axonal neuropathy in two siblings.
    Quinlivan RM, Robb SA, Hall SM, Honavar M, Hughes RA, Dubowitz V.
    Neuromuscul Disord; 1994 May 08; 4(3):227-32. PubMed ID: 7919970
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  • 38. Ultrastructural changes in peripheral nerve in hereditary motor and sensory neuropathy-Lom.
    King RH, Tournev I, Colomer J, Merlini L, Kalaydjieva L, Thomas PK.
    Neuropathol Appl Neurobiol; 1999 Aug 08; 25(4):306-12. PubMed ID: 10476047
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  • 39. 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 08; 107(2):145-54. PubMed ID: 1564512
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  • 40. [Sensori-motor neuropathy associated with congenital bilateral club feet: histological and ultrastructural study of the sural nerve].
    Yoshimura N, Fukuhara N, Noguchi T.
    No To Shinkei; 1988 Sep 08; 40(9):857-61. PubMed ID: 3190934
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