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PUBMED FOR HANDHELDS

Journal Abstract Search


293 related items for PubMed ID: 15358725

  • 1. Molecular genetics of distal hereditary motor neuropathies.
    Irobi J, De Jonghe P, Timmerman V.
    Hum Mol Genet; 2004 Oct 01; 13 Spec No 2():R195-202. PubMed ID: 15358725
    [Abstract] [Full Text] [Related]

  • 2. [Molecular genetics of inherited neuropathies].
    Takashima H.
    Rinsho Shinkeigaku; 2006 Jan 01; 46(1):1-18. PubMed ID: 16541790
    [Abstract] [Full Text] [Related]

  • 3. A molecular genetic update of inherited distal motor neuropathies.
    Irobi-Devolder J.
    Verh K Acad Geneeskd Belg; 2008 Jan 01; 70(1):25-46. PubMed ID: 18512357
    [Abstract] [Full Text] [Related]

  • 4. [The genetics of type 1 Charcot-Marie-Tooth disease, the hereditary focal neuropathies and the hereditary distal motor neuropathies].
    Sevilla T.
    Rev Neurol; 2008 Jan 01; 30(1):71-9. PubMed ID: 10743001
    [Abstract] [Full Text] [Related]

  • 5. Disease mechanisms in hereditary sensory and autonomic neuropathies.
    Verpoorten N, De Jonghe P, Timmerman V.
    Neurobiol Dis; 2006 Feb 01; 21(2):247-55. PubMed ID: 16183296
    [Abstract] [Full Text] [Related]

  • 6. [From gene to disease; Charcot-Marie-Tooth disease or the hereditary motor and sensory neuropathies].
    Verhamme C, Baas F.
    Ned Tijdschr Geneeskd; 2005 Jul 02; 149(27):1505-9. PubMed ID: 16032995
    [Abstract] [Full Text] [Related]

  • 7. Unraveling the genetics of distal hereditary motor neuronopathies.
    Irobi J, Dierick I, Jordanova A, Claeys KG, De Jonghe P, Timmerman V.
    Neuromolecular Med; 2006 Jul 02; 8(1-2):131-46. PubMed ID: 16775372
    [Abstract] [Full Text] [Related]

  • 8. Recessively transmitted predominantly motor neuropathies.
    Parman Y, Battaloğlu E.
    Handb Clin Neurol; 2013 Jul 02; 115():847-61. PubMed ID: 23931818
    [Abstract] [Full Text] [Related]

  • 9. Charcot-Marie-Tooth disease: a clinico-genetic confrontation.
    Barisic N, Claeys KG, Sirotković-Skerlev M, Löfgren A, Nelis E, De Jonghe P, Timmerman V.
    Ann Hum Genet; 2008 May 02; 72(Pt 3):416-41. PubMed ID: 18215208
    [Abstract] [Full Text] [Related]

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  • 11. [Distal hereditary motor neuropathy].
    Devic P, Petiot P.
    Rev Neurol (Paris); 2011 Nov 02; 167(11):781-90. PubMed ID: 21529868
    [Abstract] [Full Text] [Related]

  • 12. Charcot-Marie-Tooth disease and related peripheral neuropathies.
    De Jonghe P, Timmerman V, Nelis E, Martin JJ, Van Broeckhoven C.
    J Peripher Nerv Syst; 1997 Nov 02; 2(4):370-87. PubMed ID: 10975746
    [Abstract] [Full Text] [Related]

  • 13. Hereditary motor-sensory neuropathies. Charcot-Marie-Tooth syndrome.
    Bird TD.
    Neurol Clin; 1989 Feb 02; 7(1):9-23. PubMed ID: 2646524
    [Abstract] [Full Text] [Related]

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  • 15. Molecular genetics of inherited peripheral neuropathies: who are the actors?
    Meuleman J, Timmerman V, Nelis E, De Jonghe P.
    Acta Neurol Belg; 2000 Sep 02; 100(3):171-80. PubMed ID: 11098291
    [Abstract] [Full Text] [Related]

  • 16. Distal Hereditary Motor Neuropathy Type II (Distal HMN Type II): Phenotype and Molecular Genetics.
    Timmerman V, Beuten J, Irobi J, De Jonghe P, Martin JJ, VAN Broeckhoven C.
    Ann N Y Acad Sci; 1999 Oct 02; 883(1):60-64. PubMed ID: 29086966
    [Abstract] [Full Text] [Related]

  • 17. [Distal hereditary motor neuropathy type II with mutation in heat shock protein 27 gene. A case report].
    Nishibayashi M, Kokubun N, Nakamura A, Hirata K, Yamamoto M, Sobue G.
    Rinsho Shinkeigaku; 2007 Jan 02; 47(1):50-2. PubMed ID: 17491338
    [Abstract] [Full Text] [Related]

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  • 19. 2nd Workshop of the European CMT Consortium: 53rd ENMC International Workshop on Classification and Diagnostic Guidelines for Charcot-Marie-Tooth Type 2 (CMT2-HMSN II) and Distal Hereditary Motor Neuropathy (distal HMN-Spinal CMT) 26-28 September 1997, Naarden, The Netherlands.
    Neuromuscul Disord; 1998 Aug 02; 8(6):426-31. PubMed ID: 9713862
    [No Abstract] [Full Text] [Related]

  • 20. Autosomal dominant hereditary sensory neuropathy with chronic cough and gastro-oesophageal reflux: clinical features in two families linked to chromosome 3p22-p24.
    Spring PJ, Kok C, Nicholson GA, Ing AJ, Spies JM, Bassett ML, Cameron J, Kerlin P, Bowler S, Tuck R, Pollard JD.
    Brain; 2005 Dec 02; 128(Pt 12):2797-810. PubMed ID: 16311270
    [Abstract] [Full Text] [Related]


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