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Journal Abstract Search

167 related items for PubMed ID: 1857496

  • 41. Chronic inflammatory demyelinating polyneuropathy in two siblings.
    Gabreëls-Festen AA, Hageman AT, Gabreëls FJ, Joosten EM, Renier WO, Weemaes CM, ter Laak HJ.
    J Neurol Neurosurg Psychiatry; 1986 Feb; 49(2):152-6. PubMed ID: 3456424
    [Abstract] [Full Text] [Related]

  • 42. Andermann syndrome can be a phenocopy of hereditary motor and sensory neuropathy--report of a discordant sibship with a compound heterozygous mutation of the KCC3 gene.
    Rudnik-Schöneborn S, Hehr U, von Kalle T, Bornemann A, Winkler J, Zerres K.
    Neuropediatrics; 2009 Jun; 40(3):129-33. PubMed ID: 20020398
    [Abstract] [Full Text] [Related]

  • 43. Congenital hypomyelinating neuropathy: two patients with long-term follow-up.
    Phillips JP, Warner LE, Lupski JR, Garg BP.
    Pediatr Neurol; 1999 Mar; 20(3):226-32. PubMed ID: 10207934
    [Abstract] [Full Text] [Related]

  • 44. Hypertrophic neuropathy with complete conduction block-- hereditary motor and sensory neuropathy type III.
    Yim SY, Lee IY, Moon HW, Rah UW, Kim SH, Shim C, Joo HJ.
    Yonsei Med J; 1995 Nov; 36(5):466-72. PubMed ID: 8546006
    [Abstract] [Full Text] [Related]

  • 45. MRI of peripheral nerves and pathology of sural nerves in hereditary motor and sensory neuropathy type III.
    Tachi N, Kozuka N, Ohya K, Chiba S, Naganuma M.
    Neuroradiology; 1995 Aug; 37(6):496-9. PubMed ID: 7477868
    [Abstract] [Full Text] [Related]

  • 46. Giant axonal neuropathy: report of two siblings with endocrinological and histological studies.
    Takebe Y, Koide N, Takahashi G.
    Neuropediatrics; 1981 Nov; 12(4):392-404. PubMed ID: 6801537
    [Abstract] [Full Text] [Related]

  • 47. 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; 25(4):306-12. PubMed ID: 10476047
    [Abstract] [Full Text] [Related]

  • 48. 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; 30(11):1544-8. PubMed ID: 25694466
    [Abstract] [Full Text] [Related]

  • 49. Hereditary motor and sensory neuropathy with myelin outfolding: clinical, genetic and neuropathological study of three cases.
    Schenone A, Abbruzzese M, Uccelli A, Mandich P, James R, Bellone E, Giunchedi M, Rolando S, Capello E, Mandich R [corrected to Mandich P].
    J Neurol Sci; 1994 Mar; 122(1):20-7. PubMed ID: 8195799
    [Abstract] [Full Text] [Related]

  • 50. Hereditary motor and sensory neuropathy with calf muscle enlargement.
    Sakashita Y, Sakato S, Komai K, Takamori M.
    J Neurol Sci; 1992 Nov; 113(1):118-22. PubMed ID: 1469450
    [Abstract] [Full Text] [Related]

  • 51. [A case of hereditary motor and sensory neuropathy (HMSN) with excessive myelin outfolding with autosomal recessive inheritance].
    Ohnishi A, Narazaki O, Hanai T.
    J UOEH; 1998 Dec 01; 20(4):345-52. PubMed ID: 9883484
    [Abstract] [Full Text] [Related]

  • 52. Sural nerve pathology in TFG-associated motor neuron disease with sensory neuropathy.
    Li J, Meng L, Wu R, Xie Z, Gang Q, Zhang W, Wang Z, Yuan Y.
    Neuropathology; 2019 Jun 01; 39(3):194-199. PubMed ID: 30957313
    [Abstract] [Full Text] [Related]

  • 53. Hereditary motor and sensory neuropathy Lom type in an Italian Gypsy family.
    Merlini L, Villanova M, Sabatelli P, Trogu A, Malandrini A, Yanakiev P, Maraldi NM, Kalaydjieva L.
    Neuromuscul Disord; 1998 May 01; 8(3-4):182-5. PubMed ID: 9631399
    [Abstract] [Full Text] [Related]

  • 54. Hereditary motor and sensory neuropathy type 1 (HMSN1) associated with cranial neuropathy: an autopsy case report.
    Takase Y, Takahashi K, Takada K, Tatsumi H, Tabuchi Y.
    Acta Neurol Scand; 1990 Dec 01; 82(6):368-73. PubMed ID: 2291397
    [Abstract] [Full Text] [Related]

  • 55. 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 01; 121 ( Pt 3)():399-408. PubMed ID: 9549516
    [Abstract] [Full Text] [Related]

  • 56. Autosomal dominant HMSN with proximal involvement: new Brazilian cases.
    Patroclo CB, Lino AM, Marchiori PE, Brotto MW, Hirata MT.
    Arq Neuropsiquiatr; 2009 Sep 01; 67(3B):892-6. PubMed ID: 19838524
    [Abstract] [Full Text] [Related]

  • 57. A case of progressive hypertrophic neuropathy in childhood with facial diplegia (Dejerine-Sottas disease).
    Sunwoo IN, Kim JS, Chi JG, Suh YL.
    Yonsei Med J; 1988 Sep 01; 29(3):278-85. PubMed ID: 3195160
    [No Abstract] [Full Text] [Related]

  • 58. Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding in two siblings.
    Barbieri F, Santangelo R, Capparelli G, Ciccarelli A, Crisci C.
    Can J Neurol Sci; 1994 Feb 01; 21(1):29-33. PubMed ID: 8180900
    [Abstract] [Full Text] [Related]

  • 59. Hereditary motor and sensory neuropathies. Present status of types I, II and III.
    Gabreëls-Festen AA, Gabreëls FJ, Jennekens FG.
    Clin Neurol Neurosurg; 1993 Jun 01; 95(2):93-107. PubMed ID: 8344020
    [No Abstract] [Full Text] [Related]

  • 60. Mutations in the 5' region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelin.
    Houlden H, King RH, Wood NW, Thomas PK, Reilly MM.
    Brain; 2001 May 01; 124(Pt 5):907-15. PubMed ID: 11335693
    [Abstract] [Full Text] [Related]

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