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

PUBMED FOR HANDHELDS

Journal Abstract Search

391 related items for PubMed ID: 11992570

  • 1. Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.
    Brkanac Z, Fernandez M, Matsushita M, Lipe H, Wolff J, Bird TD, Raskind WH.
    Am J Med Genet; 2002 May 08; 114(4):450-7. PubMed ID: 11992570
    [Abstract] [Full Text] [Related]

  • 2. Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p.
    Stevanin G, Bouslam N, Thobois S, Azzedine H, Ravaux L, Boland A, Schalling M, Broussolle E, Dürr A, Brice A.
    Ann Neurol; 2004 Jan 08; 55(1):97-104. PubMed ID: 14705117
    [Abstract] [Full Text] [Related]

  • 3. Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6.
    Yu GY, Howell MJ, Roller MJ, Xie TD, Gomez CM.
    Ann Neurol; 2005 Mar 08; 57(3):349-54. PubMed ID: 15732118
    [Abstract] [Full Text] [Related]

  • 4. Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21.
    Verbeek DS, Schelhaas JH, Ippel EF, Beemer FA, Pearson PL, Sinke RJ.
    Hum Genet; 2002 Oct 08; 111(4-5):388-93. PubMed ID: 12384780
    [Abstract] [Full Text] [Related]

  • 5. 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 08; 128(Pt 12):2797-810. PubMed ID: 16311270
    [Abstract] [Full Text] [Related]

  • 6. Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3.
    Verbeek DS, van de Warrenburg BP, Wesseling P, Pearson PL, Kremer HP, Sinke RJ.
    Brain; 2004 Nov 08; 127(Pt 11):2551-7. PubMed ID: 15306549
    [Abstract] [Full Text] [Related]

  • 7. Hereditary motor and sensory neuropathy with proximal dominancy in the lower extremities, urinary disturbance, and paroxysmal dry cough.
    Miura S, Shibata H, Kida H, Noda K, Tomiyasu K, Yamamoto K, Iwaki A, Ayabe M, Aizawa H, Taniwaki T, Fukumaki Y.
    J Neurol Sci; 2008 Oct 15; 273(1-2):88-92. PubMed ID: 18662816
    [Abstract] [Full Text] [Related]

  • 8. A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34.
    Thiffault I, Rioux MF, Tetreault M, Jarry J, Loiselle L, Poirier J, Gros-Louis F, Mathieu J, Vanasse M, Rouleau GA, Bouchard JP, Lesage J, Brais B.
    Brain; 2006 Sep 15; 129(Pt 9):2332-40. PubMed ID: 16672289
    [Abstract] [Full Text] [Related]

  • 9. The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3.
    Nicholson GA, Dawkins JL, Blair IP, Kennerson ML, Gordon MJ, Cherryson AK, Nash J, Bananis T.
    Nat Genet; 1996 May 15; 13(1):101-4. PubMed ID: 8673084
    [Abstract] [Full Text] [Related]

  • 10. [Spinocerebellar ataxia 1--clinical study of 17 patients in a large pedigree].
    Sasaki H, Wakisaka A, Koyama T, Hamada T, Shima K, Tashiro K, Hashimoto K, Miyagishi T.
    No To Shinkei; 1993 Jun 15; 45(6):502-8. PubMed ID: 8363844
    [Abstract] [Full Text] [Related]

  • 11. An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
    Waters MF, Fee D, Figueroa KP, Nolte D, Müller U, Advincula J, Coon H, Evidente VG, Pulst SM.
    Neurology; 2005 Oct 11; 65(7):1111-3. PubMed ID: 16135769
    [Abstract] [Full Text] [Related]

  • 12. A new type of hereditary motor and sensory neuropathy linked to chromosome 3.
    Takashima H, Nakagawa M, Nakahara K, Suehara M, Matsuzaki T, Higuchi I, Higa H, Arimura K, Iwamasa T, Izumo S, Osame M.
    Ann Neurol; 1997 Jun 11; 41(6):771-80. PubMed ID: 9189038
    [Abstract] [Full Text] [Related]

  • 13. Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region.
    Hellenbroich Y, Bubel S, Pawlack H, Opitz S, Vieregge P, Schwinger E, Zühlke C.
    J Neurol; 2003 Jun 11; 250(6):668-71. PubMed ID: 12796826
    [Abstract] [Full Text] [Related]

  • 14. [Autosomal dominant cortical cerebellar atrophy (ADCCA) linked to chromosome 16q].
    Ishikawa K.
    Rinsho Shinkeigaku; 2001 Dec 11; 41(12):1117-9. PubMed ID: 12235813
    [Abstract] [Full Text] [Related]

  • 15. A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p.
    Vahedi K, Joutel A, Van Bogaert P, Ducros A, Maciazeck J, Bach JF, Bousser MG, Tournier-Lasserve E.
    Ann Neurol; 1995 Mar 11; 37(3):289-93. PubMed ID: 7695228
    [Abstract] [Full Text] [Related]

  • 16. Confirmation of a hereditary motor and sensory neuropathy IIC locus at chromosome 12q23-q24.
    McEntagart ME, Reid SL, Irrthum A, Douglas JB, Eyre KE, Donaghy MJ, Anderson NE, Rahman N.
    Ann Neurol; 2005 Feb 11; 57(2):293-7. PubMed ID: 15668982
    [Abstract] [Full Text] [Related]

  • 17. Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?
    Lohmann-Hedrich K, Neumann A, Kleensang A, Lohnau T, Muhle H, Djarmati A, König IR, Pramstaller PP, Schwinger E, Kramer PL, Ziegler A, Stephani U, Klein C.
    Neurology; 2008 Feb 26; 70(9):686-94. PubMed ID: 18032746
    [Abstract] [Full Text] [Related]

  • 18. A novel form of distal hereditary motor neuronopathy maps to chromosome 9p21.1-p12.
    Christodoulou K, Zamba E, Tsingis M, Mubaidin A, Horani K, Abu-Sheik S, El-Khateeb M, Kyriacou K, Kyriakides T, Al-Qudah AK, Middleton L.
    Ann Neurol; 2000 Dec 26; 48(6):877-84. PubMed ID: 11117544
    [Abstract] [Full Text] [Related]

  • 19. A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia.
    Cader MZ, Steckley JL, Dyment DA, McLachlan RS, Ebers GC.
    Neurology; 2005 Jul 12; 65(1):156-8. PubMed ID: 16009908
    [Abstract] [Full Text] [Related]

  • 20. Familial Behr syndrome-like phenotype with autosomal dominant inheritance.
    Felicio AC, Godeiro-Junior C, Alberto LG, Pinto AP, Sallum JM, Teive HG, Barsottini OG.
    Parkinsonism Relat Disord; 2008 Jul 12; 14(4):370-2. PubMed ID: 17977780
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 20.