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Journal Abstract Search

852 related items for PubMed ID: 18032746

  • 1. 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]

  • 2. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
    Winkelmann J, Lichtner P, Pütz B, Trenkwalder C, Hauk S, Meitinger T, Strom T, Muller-Myhsok B.
    Mov Disord; 2006 Jan 26; 21(1):28-33. PubMed ID: 16124010
    [Abstract] [Full Text] [Related]

  • 3. Childhood-onset restless legs syndrome: clinical and genetic features of 22 families.
    Muhle H, Neumann A, Lohmann-Hedrich K, Lohnau T, Lu Y, Winkler S, Waltz S, Fischenbeck A, Kramer PL, Klein C, Stephani U.
    Mov Disord; 2008 Jun 15; 23(8):1113-21; quiz 1203. PubMed ID: 18381645
    [Abstract] [Full Text] [Related]

  • 4. Family-based association study of the restless legs syndrome loci 2 and 3 in a European population.
    Kemlink D, Polo O, Montagna P, Provini F, Stiasny-Kolster K, Oertel W, de Weerd A, Nevsimalova S, Sonka K, Högl B, Frauscher B, Poewe W, Trenkwalder C, Pramstaller PP, Ferini-Strambi L, Zucconi M, Konofal E, Arnulf I, Hadjigeorgiou GM, Happe S, Klein C, Hiller A, Lichtner P, Meitinger T, Müller-Myshok B, Winkelmann J.
    Mov Disord; 2007 Jan 15; 22(2):207-12. PubMed ID: 17133505
    [Abstract] [Full Text] [Related]

  • 5. Linkage analysis of the candidate genes of familial restless legs syndrome.
    Li J, Hu LD, Wang WJ, Chen YG, Kong XY.
    Yi Chuan Xue Bao; 2003 Apr 15; 30(4):325-9. PubMed ID: 12812056
    [Abstract] [Full Text] [Related]

  • 6. Autosomal dominant restless legs syndrome maps to chromosome 20p13 (RLS-5) in a Dutch kindred.
    Sas AM, Di Fonzo A, Bakker SL, Simons EJ, Oostra BA, Maat-Kievit AJ, Boon AJ, Bonifati V.
    Mov Disord; 2010 Aug 15; 25(11):1715-22. PubMed ID: 20645405
    [Abstract] [Full Text] [Related]

  • 7. RLS3: fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity.
    Liebetanz KM, Winkelmann J, Trenkwalder C, Pütz B, Dichgans M, Gasser T, Müller-Myhsok B.
    Neurology; 2006 Jul 25; 67(2):320-1. PubMed ID: 16864828
    [Abstract] [Full Text] [Related]

  • 8. Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13.
    Kemlink D, Plazzi G, Vetrugno R, Provini F, Polo O, Stiasny-Kolster K, Oertel W, Nevsimalova S, Sonka K, Högl B, Frauscher B, Hadjigeorgiou GM, Pramstaller PP, Lichtner P, Meitinger T, Müller-Myshok B, Winkelmann J, Montagna P.
    Neurogenetics; 2008 May 25; 9(2):75-82. PubMed ID: 18193462
    [Abstract] [Full Text] [Related]

  • 9. Restless legs syndrome: epidemiological and clinicogenetic study in a South Tyrolean population isolate.
    Vogl FD, Pichler I, Adel S, Pinggera GK, Bracco S, De Grandi A, Volpato CB, Aridon P, Mayer T, Meitinger T, Klein C, Casari G, Pramstaller PP.
    Mov Disord; 2006 Aug 25; 21(8):1189-95. PubMed ID: 16685686
    [Abstract] [Full Text] [Related]

  • 10. A novel locus for restless legs syndrome on chromosome 13q.
    Balaban H, Bayrakli F, Kartal U, Pinarbasi E, Topaktas S, Kars HZ.
    Eur Neurol; 2012 Aug 25; 68(2):111-6. PubMed ID: 22797413
    [Abstract] [Full Text] [Related]

  • 11. Restless legs syndrome: an update on genetics and future perspectives.
    Pichler I, Hicks AA, Pramstaller PP.
    Clin Genet; 2008 Apr 25; 73(4):297-305. PubMed ID: 18070136
    [Abstract] [Full Text] [Related]

  • 12. A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13.
    Levchenko A, Provost S, Montplaisir JY, Xiong L, St-Onge J, Thibodeau P, Rivière JB, Desautels A, Turecki G, Dubé MP, Rouleau GA.
    Neurology; 2006 Sep 12; 67(5):900-1. PubMed ID: 16966564
    [Abstract] [Full Text] [Related]

  • 13. Autosomal-dominant locus for Restless Legs Syndrome in French-Canadians on chromosome 16p12.1.
    Levchenko A, Montplaisir JY, Asselin G, Provost S, Girard SL, Xiong L, Lemyre E, St-Onge J, Thibodeau P, Desautels A, Turecki G, Gaspar C, Dubé MP, Rouleau GA.
    Mov Disord; 2009 Jan 15; 24(1):40-50. PubMed ID: 18946881
    [Abstract] [Full Text] [Related]

  • 14. Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome.
    Winkelmann J, Lichtner P, Schormair B, Uhr M, Hauk S, Stiasny-Kolster K, Trenkwalder C, Paulus W, Peglau I, Eisensehr I, Illig T, Wichmann HE, Pfister H, Golic J, Bettecken T, Pütz B, Holsboer F, Meitinger T, Müller-Myhsok B.
    Mov Disord; 2008 Feb 15; 23(3):350-8. PubMed ID: 18058820
    [Abstract] [Full Text] [Related]

  • 15. Genetic aspects of restless legs syndrome.
    Dhawan V, Ali M, Chaudhuri KR.
    Postgrad Med J; 2006 Oct 15; 82(972):626-9. PubMed ID: 17068272
    [Abstract] [Full Text] [Related]

  • 16. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.
    Le Ber I, Camuzat A, Berger E, Hannequin D, Laquerrière A, Golfier V, Seilhean D, Viennet G, Couratier P, Verpillat P, Heath S, Camu W, Martinaud O, Lacomblez L, Vercelletto M, Salachas F, Sellal F, Didic M, Thomas-Anterion C, Puel M, Michel BF, Besse C, Duyckaerts C, Meininger V, Campion D, Dubois B, Brice A, French Research Network on FTD/FTD-MND.
    Neurology; 2009 May 12; 72(19):1669-76. PubMed ID: 19433740
    [Abstract] [Full Text] [Related]

  • 17. Genetics of restless legs syndrome.
    Winkelmann J, Ferini-Strambi L.
    Sleep Med Rev; 2006 Jun 12; 10(3):179-83. PubMed ID: 16624598
    [Abstract] [Full Text] [Related]

  • 18. The 14q restless legs syndrome locus in the French Canadian population.
    Levchenko A, Montplaisir JY, Dubé MP, Riviere JB, St-Onge J, Turecki G, Xiong L, Thibodeau P, Desautels A, Verlaan DJ, Rouleau GA.
    Ann Neurol; 2004 Jun 12; 55(6):887-91. PubMed ID: 15174026
    [Abstract] [Full Text] [Related]

  • 19. Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p.
    Chen S, Ondo WG, Rao S, Li L, Chen Q, Wang Q.
    Am J Hum Genet; 2004 May 12; 74(5):876-85. PubMed ID: 15077200
    [Abstract] [Full Text] [Related]

  • 20. Identification of a novel locus on 2q for autosomal dominant high-grade myopia.
    Paluru PC, Nallasamy S, Devoto M, Rappaport EF, Young TL.
    Invest Ophthalmol Vis Sci; 2005 Jul 12; 46(7):2300-7. PubMed ID: 15980214
    [Abstract] [Full Text] [Related]

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