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Journal Abstract Search

247 related items for PubMed ID: 15696785

  • 21. Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy.
    Plante-Bordeneuve V, Said G.
    Muscle Nerve; 2002 Nov; 26(5):608-21. PubMed ID: 12402282
    [Abstract] [Full Text] [Related]

  • 22. Autosomal-recessive and X-linked forms of hereditary motor and sensory neuropathy in childhood.
    Ouvrier R, Geevasingha N, Ryan MM.
    Muscle Nerve; 2007 Aug; 36(2):131-43. PubMed ID: 17410579
    [Abstract] [Full Text] [Related]

  • 23. [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; 40(9):857-61. PubMed ID: 3190934
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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 Sep; 147(8-9):577-85. PubMed ID: 1962067
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  • 25. Hereditary motor and sensory neuropathy type II followed in the next two generations by a clinically distal motor neuropathy.
    Selby G.
    Clin Exp Neurol; 1989 Sep; 26():65-72. PubMed ID: 2642140
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  • 26. A rare genetic disorder in the differential diagnosis of the entrapment neuropathies: hereditary neuropathy with liability to pressure palsies.
    Koc F, Güzel R, Benlidayi IC, Yerdelen D, Güzel I, Sarica Y.
    J Clin Rheumatol; 2006 Apr; 12(2):78-82. PubMed ID: 16601541
    [Abstract] [Full Text] [Related]

  • 27. [A patient of Charcot-Marie-tooth disease with rigid spine and respiratory failure].
    Takamure M, Nakamuro T, Sugie K, Suzumura A, Takayanagi T.
    Rinsho Shinkeigaku; 2000 May; 40(5):433-8. PubMed ID: 11002724
    [Abstract] [Full Text] [Related]

  • 28. [A case of hereditary motor and sensory neuropathy with pyramidal tract sign, optic nerve atrophy and mental retardation].
    Adachi T, Imaoka K, Shirasawa A, Yamaguchi S, Kobayashi S.
    Rinsho Shinkeigaku; 1998 Dec; 38(12):1037-41. PubMed ID: 10349345
    [Abstract] [Full Text] [Related]

  • 29. [Hereditary neuropathy with liability to pressure palsies in childhood].
    de las Cuevas I, Arteaga R, García A, Herranz JL.
    Rev Neurol; 1998 Dec; 31(1):38-41. PubMed ID: 10948581
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  • 31. The application of nerve conduction and clinical studies to genetic counseling in hereditary motor and sensory neuropathy type I.
    Berciano J, Combarros O, Calleja J, Polo JM, Leno C.
    Muscle Nerve; 1989 Apr; 12(4):302-6. PubMed ID: 2770783
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  • 35. Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1.
    Tazir M, Vallat JM, Bomont P, Zemmouri R, Sindou P, Assami S, Nouioua S, Hammadouche T, Grid D, Koenig M.
    Neuromuscul Disord; 2002 Nov; 12(9):849-52. PubMed ID: 12398836
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  • 37. [Clinical report of hereditary motor and sensory neuropathy with proximal dominance in Shiga prefecture].
    Takahashi M, Mitsui Y, Yorifuji S, Nakamura Y, Tsukamoto Y, Nishimoto K.
    Rinsho Shinkeigaku; 2007 Sep; 47(9):571-6. PubMed ID: 18018614
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  • 38. Hereditary neuropathy with liability to pressure palsies in a Turkish patient (HNPP): a rare cause of entrapment neuropathies in young adults.
    Celik Y, Kilinçer C, Hamamcioğlu MK, Balci K, Birgili B, Cobanoğlu S, Utku U.
    Turk Neurosurg; 2008 Jan; 18(1):82-4. PubMed ID: 18382985
    [Abstract] [Full Text] [Related]

  • 39. Congenital giant axonal neuropathy.
    Kinney RB, Gottfried MR, Hodson AK, Autilio-Gambetti L, Graham DG.
    Arch Pathol Lab Med; 1985 Jul; 109(7):639-41. PubMed ID: 2990373
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