These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


184 related items for PubMed ID: 8659534

  • 1. Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2B.
    Vance JM, Speer MC, Stajich JM, West S, Wolpert C, Gaskell P, Lennon F, Tim RM, Rozear M, Othmane KB.
    Am J Hum Genet; 1996 Jul; 59(1):258-62. PubMed ID: 8659534
    [No Abstract] [Full Text] [Related]

  • 2. Hereditary sensory neuropathies.
    Houlden H, Blake J, Reilly MM.
    Curr Opin Neurol; 2004 Oct; 17(5):569-77. PubMed ID: 15367861
    [Abstract] [Full Text] [Related]

  • 3. Classifications of neurogenetic diseases: An increasingly complex problem.
    Vallat JM, Goizet C, Tazir M, Couratier P, Magy L, Mathis S.
    Rev Neurol (Paris); 2016 Oct; 172(6-7):339-49. PubMed ID: 27240993
    [Abstract] [Full Text] [Related]

  • 4. Charcot-Marie-Tooth disease (hereditary motor sensory neuropathies) and hereditary sensory and autonomic neuropathies.
    Bertorini T, Narayanaswami P, Rashed H.
    Neurologist; 2004 Nov; 10(6):327-37. PubMed ID: 15518599
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Evidence for linkage of type I hereditary motor and sensory neuropathy to the Duffy locus on chromosome 1.
    Guiloff RJ, Thomas PK, Contreras M, Armitage S, Schwarz G, Sedgwick EM.
    Ann Hum Genet; 1982 Jan 01; 46(1):25-7. PubMed ID: 6954871
    [No Abstract] [Full Text] [Related]

  • 7. Sorting out the inherited neuropathies.
    Reilly MM.
    Pract Neurol; 2007 Apr 01; 7(2):93-105. PubMed ID: 17430873
    [No Abstract] [Full Text] [Related]

  • 8. Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I loci.
    Auer-Grumbach M, Wagner K, Timmerman V, De Jonghe P, Hartung HP.
    Neurology; 2000 Jan 11; 54(1):45-52. PubMed ID: 10636124
    [Abstract] [Full Text] [Related]

  • 9. Diagnosis and new treatments in genetic neuropathies.
    Reilly MM, Shy ME.
    J Neurol Neurosurg Psychiatry; 2009 Dec 11; 80(12):1304-14. PubMed ID: 19917815
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. [Genetics of neuropathies].
    Gess B, Schirmacher A, Young P.
    Nervenarzt; 2013 Feb 11; 84(2):157-65. PubMed ID: 23325310
    [Abstract] [Full Text] [Related]

  • 14. [Hereditary sensory and motor neuropathy and hereditary sensory and autonomic neuropathies: recent advances].
    Stojkovic T.
    Rev Neurol (Paris); 2011 Dec 11; 167(12):948-50. PubMed ID: 22100327
    [Abstract] [Full Text] [Related]

  • 15. [The genetics of type 1 Charcot-Marie-Tooth disease, the hereditary focal neuropathies and the hereditary distal motor neuropathies].
    Sevilla T.
    Rev Neurol; 2011 Dec 11; 30(1):71-9. PubMed ID: 10743001
    [Abstract] [Full Text] [Related]

  • 16. [Hereditary neuropathies].
    Mellgren SI, Vedeler C.
    Tidsskr Nor Laegeforen; 2003 Sep 25; 123(18):2585-7. PubMed ID: 14714050
    [Abstract] [Full Text] [Related]

  • 17. [Molecular genetic diagnosis of Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies].
    Aarskog NK, Vedeler CA.
    Tidsskr Nor Laegeforen; 2002 Feb 10; 122(4):382-5. PubMed ID: 11915667
    [Abstract] [Full Text] [Related]

  • 18. Genetic evaluation of inherited motor/sensory neuropathy.
    Chance PF.
    Suppl Clin Neurophysiol; 2004 Feb 10; 57():228-42. PubMed ID: 16106622
    [Abstract] [Full Text] [Related]

  • 19. Genetically determined neuropathies.
    Reilly MM.
    J Neurol; 1998 Jan 10; 245(1):6-13. PubMed ID: 9457622
    [Abstract] [Full Text] [Related]

  • 20. A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotype.
    De Jonghe P, Timmerman V, Nelis E, De Vriendt E, Löfgren A, Ceuterick C, Martin JJ, Van Broeckhoven C.
    Arch Neurol; 1999 Oct 10; 56(10):1283-8. PubMed ID: 10520946
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 10.