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 *

202 related articles for article (PubMed ID: 18325672)

  • 81. Mapping of autosomal dominant cerebellar ataxia without the pathogenic PPP2R2B mutation to the locus for spinocerebellar ataxia 12.
    Sato K; Yabe I; Fukuda Y; Soma H; Nakahara Y; Tsuji S; Sasaki H
    Arch Neurol; 2010 Oct; 67(10):1257-62. PubMed ID: 20937954
    [TBL] [Abstract][Full Text] [Related]  

  • 82. Spinocerebellar ataxias in Brazil--frequencies and modulating effects of related genes.
    de Castilhos RM; Furtado GV; Gheno TC; Schaeffer P; Russo A; Barsottini O; Pedroso JL; Salarini DZ; Vargas FR; de Lima MA; Godeiro C; Santana-da-Silva LC; Toralles MB; Santos S; van der Linden H; Wanderley HY; de Medeiros PF; Pereira ET; Ribeiro E; Saraiva-Pereira ML; Jardim LB;
    Cerebellum; 2014 Feb; 13(1):17-28. PubMed ID: 23943520
    [TBL] [Abstract][Full Text] [Related]  

  • 83. Two young sisters with spinocerebellar ataxia type 2 showing different clinical progression of disease.
    Yiş U; Dirik E; Kurul SH; Eken AG; Başak AN
    Cerebellum; 2009 Jun; 8(2):127-9. PubMed ID: 19023636
    [TBL] [Abstract][Full Text] [Related]  

  • 84. Amyotrophic lateral sclerosis and spinocerebellar ataxia type 2 in a family with full CAG repeat expansions of ATXN2.
    Tazen S; Figueroa K; Kwan JY; Goldman J; Hunt A; Sampson J; Gutmann L; Pulst SM; Mitsumoto H; Kuo SH
    JAMA Neurol; 2013 Oct; 70(10):1302-4. PubMed ID: 23959108
    [TBL] [Abstract][Full Text] [Related]  

  • 85. Genomic organisation of the spinocerebellar ataxia type 7 (SCA7) gene responsible for autosomal dominant cerebellar ataxia with retinal degeneration.
    Michalík A; Del-Favero J; Mauger C; Löfgren A; Van Broeckhoven C
    Hum Genet; 1999 Nov; 105(5):410-7. PubMed ID: 10598805
    [TBL] [Abstract][Full Text] [Related]  

  • 86. Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese families.
    Basri R; Yabe I; Soma H; Sasaki H
    J Hum Genet; 2007; 52(10):848-855. PubMed ID: 17805477
    [TBL] [Abstract][Full Text] [Related]  

  • 87. Bidirectional expression of the SCA8 expansion mutation: one mutation, two genes.
    Ikeda Y; Daughters RS; Ranum LP
    Cerebellum; 2008; 7(2):150-8. PubMed ID: 18418692
    [TBL] [Abstract][Full Text] [Related]  

  • 88. Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion.
    Obayashi M; Stevanin G; Synofzik M; Monin ML; Duyckaerts C; Sato N; Streichenberger N; Vighetto A; Desestret V; Tesson C; Wichmann HE; Illig T; Huttenlocher J; Kita Y; Izumi Y; Mizusawa H; Schöls L; Klopstock T; Brice A; Ishikawa K; Dürr A
    J Neurol Neurosurg Psychiatry; 2015 Sep; 86(9):986-95. PubMed ID: 25476002
    [TBL] [Abstract][Full Text] [Related]  

  • 89. Metabolic and Organelle Morphology Defects in Mice and Human Patients Define Spinocerebellar Ataxia Type 7 as a Mitochondrial Disease.
    Ward JM; Stoyas CA; Switonski PM; Ichou F; Fan W; Collins B; Wall CE; Adanyeguh I; Niu C; Sopher BL; Kinoshita C; Morrison RS; Durr A; Muotri AR; Evans RM; Mochel F; La Spada AR
    Cell Rep; 2019 Jan; 26(5):1189-1202.e6. PubMed ID: 30699348
    [TBL] [Abstract][Full Text] [Related]  

  • 90. Spinocerebellar ataxia type 7 with
    Park JY; Wy SY; Joo K; Woo SJ
    Ophthalmic Genet; 2019 Jun; 40(3):282-285. PubMed ID: 31269856
    [No Abstract]   [Full Text] [Related]  

  • 91. Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14.
    Chelban V; Wiethoff S; Fabian-Jessing BK; Haridy NA; Khan A; Efthymiou S; Becker EBE; O'Connor E; Hersheson J; Newland K; Hojland AT; Gregersen PA; Lindquist SG; Petersen MB; Nielsen JE; Nielsen M; Wood NW; Giunti P; Houlden H
    Mov Disord; 2018 Jul; 33(7):1119-1129. PubMed ID: 29603387
    [TBL] [Abstract][Full Text] [Related]  

  • 92. Molecular spectrum, family screening and genetic counselling of Spinocerebellar Ataxia (SCA) cases in an Indian scenario.
    Vishwakarma P; Agarwal S; Dean DD; Muthuswamy S; Mandal K
    J Neurogenet; 2021; 35(4):370-380. PubMed ID: 34159894
    [TBL] [Abstract][Full Text] [Related]  

  • 93. Focal dystonia as a presenting sign of spinocerebellar ataxia 17.
    Hagenah JM; Zühlke C; Hellenbroich Y; Heide W; Klein C
    Mov Disord; 2004 Feb; 19(2):217-20. PubMed ID: 14978680
    [TBL] [Abstract][Full Text] [Related]  

  • 94. Clinical and molecular correlations in spinocerebellar ataxia type 6: a study of 24 Dutch families.
    Sinke RJ; Ippel EF; Diepstraten CM; Beemer FA; Wokke JH; van Hilten BJ; Knoers NV; van Amstel HK; Kremer HP
    Arch Neurol; 2001 Nov; 58(11):1839-44. PubMed ID: 11708993
    [TBL] [Abstract][Full Text] [Related]  

  • 95. [Frequency analysis of autosomal dominant spinocerebellar ataxias in Han population in the Chinese mainland and clinical and molecular characterization of spinocerebellar ataxia type 6].
    Jiang H; Tang B; Xu B; Zhao GH; Shen L; Tang JG; Li QH; Xia K
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):1-4. PubMed ID: 15696468
    [TBL] [Abstract][Full Text] [Related]  

  • 96. Spinocerebellar ataxia type 7 (SCA7): first report of a systematic neuropathological study of the brain of a patient with a very short expanded CAG-repeat.
    Rüb U; Brunt ER; Gierga K; Seidel K; Schultz C; Schöls L; Auburger G; Heinsen H; Ippel PF; Glimmerveen WF; Wittebol-Post D; Arai K; Deller T; de Vos RA
    Brain Pathol; 2005 Oct; 15(4):287-95. PubMed ID: 16389941
    [TBL] [Abstract][Full Text] [Related]  

  • 97. An expanded CAG repeat sequence in spinocerebellar ataxia type 7.
    Lindblad K; Savontaus ML; Stevanin G; Holmberg M; Digre K; Zander C; Ehrsson H; David G; Benomar A; Nikoskelainen E; Trottier Y; Holmgren G; Ptacek LJ; Anttinen A; Brice A; Schalling M
    Genome Res; 1996 Oct; 6(10):965-71. PubMed ID: 8908515
    [TBL] [Abstract][Full Text] [Related]  

  • 98. Comparison of an expanded ataxia interactome with patient medical records reveals a relationship between macular degeneration and ataxia.
    Kahle JJ; Gulbahce N; Shaw CA; Lim J; Hill DE; Barabási AL; Zoghbi HY
    Hum Mol Genet; 2011 Feb; 20(3):510-27. PubMed ID: 21078624
    [TBL] [Abstract][Full Text] [Related]  

  • 99. Autosomal dominant spinocerebellar ataxias: an Asian perspective.
    Tan EK
    Can J Neurol Sci; 2003 Nov; 30(4):361-7. PubMed ID: 14672269
    [TBL] [Abstract][Full Text] [Related]  

  • 100. Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine disease.
    Wallenius J; Kafantari E; Jhaveri E; Gorcenco S; Ameur A; Karremo C; Dobloug S; Karrman K; de Koning T; Ilinca A; Landqvist Waldö M; Arvidsson A; Persson S; Englund E; Ehrencrona H; Puschmann A
    Am J Hum Genet; 2024 Jan; 111(1):82-95. PubMed ID: 38035881
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.