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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

116 related items for PubMed ID: 8935304

  • 41. A Dejerine-Sottas neuropathy family with a gene mapped on chromosome 8.
    Ionasescu VV, Kimura J, Searby CC, Smith WL, Ross MA, Ionasescu R.
    Muscle Nerve; 1996 Mar; 19(3):319-23. PubMed ID: 8606695
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  • 42. Sensory neuropathy with onion-bulb formation. Report of a case with onset in infancy.
    Koto A, Horoupian DS, Spiro A, Suzuki K, Torch WC.
    Am J Dis Child; 1978 Apr; 132(4):379-81. PubMed ID: 645656
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  • 43. [Hereditary neuropathy with liability to pressure palsy].
    Eisenberg E, Baron S, Ludicer R.
    Harefuah; 1989 Apr 02; 116(7):345-7. PubMed ID: 2737556
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  • 44. [Optic atrophy, sensorineural deafness and sensory neuropathy].
    Monge Argiles JA, Alom Poveda J, Espinosa Martínez J, Pérez Arroyo M, Roca Estelles MJ.
    Neurologia; 1994 Feb 02; 9(2):69-71. PubMed ID: 8204252
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  • 55. Muscle and intramuscular nerve pathology in congenital hypomyelination neuropathy.
    Nara T, Akashi M, Nonaka I, Nakanishi Y, Hamano S, Ochiai Y, Tsuzura S.
    J Neurol Sci; 1995 Apr 02; 129(2):170-4. PubMed ID: 7608732
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  • 56. 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 02; 36(5):466-72. PubMed ID: 8546006
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  • 57. [A case of hereditary motor and sensory neuropathy type I with optic atrophy, neural deafness and pyramidal tract signs].
    Saito T, Nishioka M, Ogino M, Endo K, Kowa H.
    Rinsho Shinkeigaku; 1993 May 02; 33(5):519-24. PubMed ID: 8365058
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  • 58. Effect of an R69C mutation in the myelin protein zero gene on myelination and ion channel subtypes.
    Bai Y, Ianokova E, Pu Q, Ghandour K, Levinson R, Martin JJ, Ceuterick-de Groote C, Mazanec R, Seeman P, Shy ME, Li J.
    Arch Neurol; 2006 Dec 02; 63(12):1787-94. PubMed ID: 17172621
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