BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

311 related articles for article (PubMed ID: 23538602)

  • 41. Analysis of spinocerebellar ataxia type 2 in Gunma Prefecture in Japan: CAG trinucleotide expansion and clinical characteristics.
    Mizushima K; Watanabe M; Abe K; Aoki M; Itoyama Y; Shizuka M; Okamoto K; Shoji M
    J Neurol Sci; 1998 Apr; 156(2):180-5. PubMed ID: 9588855
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group.
    Pujana MA; Corral J; Gratacòs M; Combarros O; Berciano J; Genís D; Banchs I; Estivill X; Volpini V
    Hum Genet; 1999 Jun; 104(6):516-22. PubMed ID: 10453742
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [Molecular and clinical features in spinocerebellar ataxia type 6 (SCA6) in Japanese].
    Ikeuchi T
    Nihon Rinsho; 1999 Apr; 57(4):891-5. PubMed ID: 10222785
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Current concepts in the treatment of hereditary ataxias.
    Braga Neto P; Pedroso JL; Kuo SH; Marcondes Junior CF; Teive HA; Barsottini OG
    Arq Neuropsiquiatr; 2016 Mar; 74(3):244-52. PubMed ID: 27050855
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and spinocerebellar ataxia type 1.
    Hashida H; Goto J; Kurisaki H; Mizusawa H; Kanazawa I
    Ann Neurol; 1997 Apr; 41(4):505-11. PubMed ID: 9124808
    [TBL] [Abstract][Full Text] [Related]  

  • 46. The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice.
    Vural A; Şimşir G; Tekgül Ş; Koçoğlu C; Akçimen F; Kartal E; Şen NE; Lahut S; Ömür Ö; Saner N; Gül T; Bayraktar E; Palvadeau R; Tunca C; Pirkevi Çetinkaya C; Gündoğdu Eken A; Şahbaz I; Kovancılar Koç M; Öztop Çakmak Ö; Hanağası H; Bilgiç B; Eraksoy M; Gündüz A; Apaydın H; Kızıltan G; Özekmekçi S; Siva A; Altıntaş A; Kaya Güleç ZE; Parman Y; Oflazer P; Deymeer F; Durmuş H; Şahin E; Çakar A; Tüfekçioğlu Z; Tektürk P; Çorbalı MO; Tireli H; Akdal G; Yiş U; Hız S; Şengün İ; Bora E; Serdaroğlu G; Erer Özbek S; Ağan K; İnce Günal D; Us Ö; Kurt SG; Aksoy D; Bora Tokçaer A; Elmas M; Gültekin M; Kumandaş S; Acer H; Kaya Özçora GD; Yayla V; Soysal A; Genç G; Güllüoğlu H; Kotan D; Özözen Ayas Z; Şahin HA; Tan E; Topçu M; Topçuoğlu ES; Akbostancı C; Koç F; Ertan S; Elibol B; Başak AN
    Mov Disord; 2021 Jul; 36(7):1676-1688. PubMed ID: 33624863
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Ataxias with autosomal, X-chromosomal or maternal inheritance.
    Finsterer J
    Can J Neurol Sci; 2009 Jul; 36(4):409-28. PubMed ID: 19650351
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Hereditary Ataxias in Cuba: A Nationwide Epidemiological and Clinical Study in 1001 Patients.
    Velázquez-Pérez L; Medrano-Montero J; Rodríguez-Labrada R; Canales-Ochoa N; Campins Alí J; Carrillo Rodes FJ; Rodríguez Graña T; Hernández Oliver MO; Aguilera Rodríguez R; Domínguez Barrios Y; Torres Vega R; Flores Angulo L; Cordero Navarro NY; Sigler Villanueva AA; Gámez Rodríguez O; Sagaró Zambrano I; Navas Napóles NY; García Zacarías J; Serrano Barrera OR; Ramírez Bautista MB; Estupiñán Rodríguez A; Guerra Rondón LA; Vázquez-Mojena Y; González-Zaldivar Y; Almaguer Mederos LE; Leyva-Mérida A;
    Cerebellum; 2020 Apr; 19(2):252-264. PubMed ID: 31981095
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Other autosomal recessive and childhood ataxias.
    De Michele G; Filla A
    Handb Clin Neurol; 2012; 103():343-57. PubMed ID: 21827899
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Hereditary ataxias and paediatric neurology: new movers and shakers enter the field.
    Morrison PJ
    Eur J Paediatr Neurol; 2003; 7(5):217-9. PubMed ID: 14511625
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Distinct phenotypes within autosomal recessive ataxias not linked to already known loci.
    Bouhlal Y; El-Euch-Fayeche G; Amouri R; Hentati F
    Acta Myol; 2005 Oct; 24(2):155-61. PubMed ID: 16550933
    [TBL] [Abstract][Full Text] [Related]  

  • 52. The inherited ataxias: genetic heterogeneity, mutation databases, and future directions in research and clinical diagnostics.
    Hersheson J; Haworth A; Houlden H
    Hum Mutat; 2012 Sep; 33(9):1324-32. PubMed ID: 22689585
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Infantile onset spinocerebellar ataxia 2 (SCA2): a clinical report with review of previous cases.
    Singh A; Faruq M; Mukerji M; Dwivedi MK; Pruthi S; Kapoor S
    J Child Neurol; 2014 Jan; 29(1):139-44. PubMed ID: 24300164
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Dominantly inherited ataxias.
    Gomez CM; Subramony SH
    Semin Pediatr Neurol; 2003 Sep; 10(3):210-22. PubMed ID: 14653409
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [Autosomal recessive cerebellar ataxias. Their classification, genetic features and pathophysiology].
    Espinós-Armero C; González-Cabo P; Palau-Martínez F
    Rev Neurol; 2005 Oct 1-15; 41(7):409-22. PubMed ID: 16193447
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Clinical spectrum of early onset cerebellar ataxia with retained tendon reflexes: an autosomal recessive ataxia not to be missed.
    Pedroso JL; Braga-Neto P; Ricarte IF; Albuquerque MV; Barsottini OG
    Arq Neuropsiquiatr; 2013 Jun; 71(6):345-8. PubMed ID: 23828538
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1.
    Flanigan K; Gardner K; Alderson K; Galster B; Otterud B; Leppert MF; Kaplan C; Ptácek LJ
    Am J Hum Genet; 1996 Aug; 59(2):392-9. PubMed ID: 8755926
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Hereditary ataxias].
    Tallaksen CM
    Tidsskr Nor Laegeforen; 2008 Sep; 128(17):1977-80. PubMed ID: 18787576
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.
    Gros-Louis F; Dupré N; Dion P; Fox MA; Laurent S; Verreault S; Sanes JR; Bouchard JP; Rouleau GA
    Nat Genet; 2007 Jan; 39(1):80-5. PubMed ID: 17159980
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Treatment for speech disorder in Friedreich ataxia and other hereditary ataxia syndromes.
    Vogel AP; Folker J; Poole ML
    Cochrane Database Syst Rev; 2014 Oct; (10):CD008953. PubMed ID: 25348587
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.