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

140 related items for PubMed ID: 14743366

  • 1. Mutational analysis of neurotensin in familial restless legs syndrome.
    Desautels A, Turecki G, Xiong L, Rochefort D, Montplaisir J, Rouleau GA.
    Mov Disord; 2004 Jan; 19(1):90-4. PubMed ID: 14743366
    [Abstract] [Full Text] [Related]

  • 2. Genetic association studies of neurotensin gene and restless legs syndrome in French Canadians.
    Xiong L, Levchenko A, Montplaisir J, Rivière JB, Thibodeau P, St-Onge J, Gaspar C, Desautels A, Lespérance P, Chouinard S, Turecki G, Rouleau GA.
    Sleep Med; 2008 Mar; 9(3):273-82. PubMed ID: 17644423
    [Abstract] [Full Text] [Related]

  • 3. 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; 21(1):28-33. PubMed ID: 16124010
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 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 26; 30(4):325-9. PubMed ID: 12812056
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity.
    Desautels A, Turecki G, Montplaisir J, Xiong L, Walters AS, Ehrenberg BL, Brisebois K, Desautels AK, Gingras Y, Johnson WG, Lugaresi E, Coccagna G, Picchietti DL, Lazzarini A, Rouleau GA.
    Arch Neurol; 2005 Apr 15; 62(4):591-6. PubMed ID: 15824258
    [Abstract] [Full Text] [Related]

  • 8. Genetics of restless legs syndrome.
    Winkelmann J, Ferini-Strambi L.
    Sleep Med Rev; 2006 Jun 15; 10(3):179-83. PubMed ID: 16624598
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Genetics in restless legs syndrome.
    Ferini-Strambi L, Bonati MT, Oldani A, Aridon P, Zucconi M, Casari G.
    Sleep Med; 2004 May 15; 5(3):301-4. PubMed ID: 15165539
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 12; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 13. Genomic structure and organization of the high grade Myopia-2 locus (MYP2) critical region: mutation screening of 9 positional candidate genes.
    Scavello GS, Paluru PC, Zhou J, White PS, Rappaport EF, Young TL.
    Mol Vis; 2005 Feb 02; 11():97-110. PubMed ID: 15723005
    [Abstract] [Full Text] [Related]

  • 14. 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 02; 55(6):887-91. PubMed ID: 15174026
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. 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]

  • 17. PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome.
    Schormair B, Kemlink D, Roeske D, Eckstein G, Xiong L, Lichtner P, Ripke S, Trenkwalder C, Zimprich A, Stiasny-Kolster K, Oertel W, Bachmann CG, Paulus W, Högl B, Frauscher B, Gschliesser V, Poewe W, Peglau I, Vodicka P, Vávrová J, Sonka K, Nevsimalova S, Montplaisir J, Turecki G, Rouleau G, Gieger C, Illig T, Wichmann HE, Holsboer F, Müller-Myhsok B, Meitinger T, Winkelmann J.
    Nat Genet; 2008 Aug 15; 40(8):946-8. PubMed ID: 18660810
    [Abstract] [Full Text] [Related]

  • 18. 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 15; 68(2):111-6. PubMed ID: 22797413
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. 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 15; 21(8):1189-95. PubMed ID: 16685686
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.