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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 16389595)

  • 41. Genetic background of apparently idiopathic sporadic cerebellar ataxia.
    Schöls L; Szymanski S; Peters S; Przuntek H; Epplen JT; Hardt C; Riess O
    Hum Genet; 2000 Aug; 107(2):132-7. PubMed ID: 11030410
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [Gene diagnosis and CAG repeat analysis of spinocerebellar ataxia cases of Guangxi region].
    Tan JQ; Wang P; Hu QP; Li SF; Shu W; Ma J; Fang L; Hua R; Ding Y; Yuan ZG
    Yi Chuan; 2009 Jun; 31(6):605-10. PubMed ID: 19586860
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Frequency analysis and clinical characterization of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Korean patients.
    Lee WY; Jin DK; Oh MR; Lee JE; Song SM; Lee EA; Kim GM; Chung JS; Lee KH
    Arch Neurol; 2003 Jun; 60(6):858-63. PubMed ID: 12810491
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Prevalence and Characteristics of Periodic Limb Movements during Sleep in Korean Adult Patients with Restless Legs Syndrome.
    Shin JW; Koo YS; Lee BU; Shin WC; Lee SK; Cho YW; Jung KY
    J Clin Sleep Med; 2016 Aug; 12(8):1089-97. PubMed ID: 27306390
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Relative contribution of SCA2, SCA3 and SCA17 in Korean patients with parkinsonism and ataxia.
    Yun JY; Lee WW; Kim HJ; Kim JS; Kim JM; Kim HJ; Kim SY; Kim JY; Park SS; Kim YK; Kim SE; Jeon BS
    Parkinsonism Relat Disord; 2011 Jun; 17(5):338-42. PubMed ID: 21334959
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Intermediate CAG repeat lengths (53,54) for MJD/SCA3 are associated with an abnormal phenotype.
    van Alfen N; Sinke RJ; Zwarts MJ; Gabreëls-Festen A; Praamstra P; Kremer BP; Horstink MW
    Ann Neurol; 2001 Jun; 49(6):805-7. PubMed ID: 11409435
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Clinical characteristics and frequency of the hereditary restless legs syndrome in a population of 300 patients.
    Winkelmann J; Wetter TC; Collado-Seidel V; Gasser T; Dichgans M; Yassouridis A; Trenkwalder C
    Sleep; 2000 Aug; 23(5):597-602. PubMed ID: 10947027
    [TBL] [Abstract][Full Text] [Related]  

  • 48. MEIS1 variant as a determinant of autonomic imbalance in Restless Legs Syndrome.
    Thireau J; Farah C; Molinari N; Bouilloux F; Torreilles L; Winkelmann J; Scholz S; Richard S; Dauvilliers Y; Marmigère F
    Sci Rep; 2017 Apr; 7():46620. PubMed ID: 28425489
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A spinocerebellar ataxia family with expanded alleles in the TATA-binding protein gene and ataxin-3 gene.
    Xu Q; Li Q; Wang J; Jiang H; Shen L; Li X; Tang B
    Int J Neurosci; 2010 Feb; 120(2):159-61. PubMed ID: 20199210
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Molecular genetic diagnosis and clinical analysis of spinocerebellar ataxia type 7].
    Xie QY; Liang XL; Li XH; Feng YQ
    Di Yi Jun Yi Da Xue Xue Bao; 2004 Jan; 24(1):62-5. PubMed ID: 14724100
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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; 23(8):1113-21; quiz 1203. PubMed ID: 18381645
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Genetic testing for spinocerebellar ataxias in patients diagnosed as Parkinson's disease in Bangladesh.
    Rahman MS; Sarkar MA; Rahman MF; Paul SK; Nagai SY; Uddin MJ; Toda T
    Mymensingh Med J; 2015 Jan; 24(1):44-51. PubMed ID: 25725667
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Gamma-aminobutyric acid (GABA) receptors genes polymorphisms and risk for restless legs syndrome.
    Jiménez-Jiménez FJ; Esguevillas G; Alonso-Navarro H; Zurdo M; Turpín-Fenoll L; Millán-Pascual J; Adeva-Bartolomé T; Cubo E; Navacerrada F; Amo G; Rojo-Sebastián A; Rubio L; Díez-Fairén M; Pastor P; Calleja M; Plaza-Nieto JF; Pilo-de-la-Fuente B; Arroyo-Solera M; García-Albea E; Agúndez JAG; García-Martín E
    Pharmacogenomics J; 2018 Jul; 18(4):565-577. PubMed ID: 29720720
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Spectral analysis of sleep EEG in patients with restless legs syndrome.
    Hornyak M; Feige B; Voderholzer U; Riemann D
    Clin Neurophysiol; 2005 Jun; 116(6):1265-72. PubMed ID: 15978488
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Leg movements during wakefulness in restless legs syndrome: time structure and relationships with periodic leg movements during sleep.
    Ferri R; Manconi M; Plazzi G; Bruni O; Cosentino FI; Ferini-Strambi L; Zucconi M
    Sleep Med; 2012 May; 13(5):529-35. PubMed ID: 22341907
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Restless legs syndrome and periodic limb movements during sleep in the Multi-Ethnic Study of Atherosclerosis.
    Doan TT; Koo BB; Ogilvie RP; Redline S; Lutsey PL
    Sleep; 2018 Aug; 41(8):. PubMed ID: 29860522
    [TBL] [Abstract][Full Text] [Related]  

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

  • 58. Identification of 46 CAG repeats within PPP2R2B as probably the shortest pathogenic allele for SCA12.
    Dong Y; Wu JJ; Wu ZY
    Parkinsonism Relat Disord; 2015 Apr; 21(4):398-401. PubMed ID: 25634432
    [TBL] [Abstract][Full Text] [Related]  

  • 59. SCA2 trinucleotide expansion in German SCA patients.
    Riess O; Laccone FA; Gispert S; Schöls L; Zühlke C; Vieira-Saecker AM; Herlt S; Wessel K; Epplen JT; Weber BH; Kreuz F; Chahrokh-Zadeh S; Meindl A; Lunkes A; Aguiar J; Macek M; Krebsová A; Macek M; Bürk K; Tinschert S; Schreyer I; Pulst SM; Auburger G
    Neurogenetics; 1997 May; 1(1):59-64. PubMed ID: 10735276
    [TBL] [Abstract][Full Text] [Related]  

  • 60. The solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene, SLC1A2, rs3794087 variant and assessment risk for restless legs syndrome.
    Jiménez-Jiménez FJ; Alonso-Navarro H; Martínez C; Zurdo M; Turpín-Fenoll L; Millán-Pascual J; Adeva-Bartolomé T; Cubo E; Navacerrada F; Rojo-Sebastián A; Rubio L; Calleja M; Plaza-Nieto JF; Pilo-de-la-Fuente B; Arroyo-Solera M; García-Martín E; Agúndez JA
    Sleep Med; 2014 Feb; 15(2):266-8. PubMed ID: 24424098
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.