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 *

132 related articles for article (PubMed ID: 31132534)

  • 1. Screening for spinocerebellar ataxia type 36 (SCA36) in the Greek population.
    Katsimpouris D; Kartanou C; Breza M; Panas M; Koutsis G; Karadima G
    J Neurol Sci; 2019 Jul; 402():131-132. PubMed ID: 31132534
    [No Abstract]   [Full Text] [Related]  

  • 2. Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes.
    Aydin G; Dekomien G; Hoffjan S; Gerding WM; Epplen JT; Arning L
    BMC Neurol; 2018 Jan; 18(1):3. PubMed ID: 29316893
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Recent advances in clinical and genetic research of spinocerebellar ataxia type 36].
    Zeng S; Tang B; Wang J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Dec; 32(6):886-9. PubMed ID: 26663071
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Spinocerebellar ataxia 36 (SCA36): «Costa da Morte ataxia».
    Arias M; García-Murias M; Sobrido MJ
    Neurologia; 2017; 32(6):386-393. PubMed ID: 25593102
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Spinocerebellar ataxia type 36 (nicknamed Asidan)].
    Abe K; Ikeda Y
    Brain Nerve; 2012 Aug; 64(8):937-41. PubMed ID: 22868885
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical features of SCA36: a novel spinocerebellar ataxia with motor neuron involvement (Asidan).
    Ikeda Y; Ohta Y; Kobayashi H; Okamoto M; Takamatsu K; Ota T; Manabe Y; Okamoto K; Koizumi A; Abe K
    Neurology; 2012 Jul; 79(4):333-41. PubMed ID: 22744658
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.
    Tang B; Liu C; Shen L; Dai H; Pan Q; Jing L; Ouyang S; Xia J
    Arch Neurol; 2000 Apr; 57(4):540-4. PubMed ID: 10768629
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spinocerebellar ataxia type 10: Frequency of epilepsy in a large sample of Brazilian patients.
    Teive HA; Munhoz RP; Raskin S; Arruda WO; de Paola L; Werneck LC; Ashizawa T
    Mov Disord; 2010 Dec; 25(16):2875-8. PubMed ID: 20818609
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and Genetic Evaluation of Spinocerebellar Ataxia Type 10 in 16 Brazilian Families.
    Domingues BMD; Nascimento FA; Meira AT; Moro A; Raskin S; Ashizawa T; Teive HAG
    Cerebellum; 2019 Oct; 18(5):849-854. PubMed ID: 31377949
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population.
    Alonso E; Martínez-Ruano L; De Biase I; Mader C; Ochoa A; Yescas P; Gutiérrez R; White M; Ruano L; Fragoso-Benítez M; Ashizawa T; Bidichandani SI; Rasmussen A
    Mov Disord; 2007 May; 22(7):1050-3. PubMed ID: 17427938
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical phenotype of Brazilian families with spinocerebellar ataxia 10.
    Teive HA; Roa BB; Raskin S; Fang P; Arruda WO; Neto YC; Gao R; Werneck LC; Ashizawa T
    Neurology; 2004 Oct; 63(8):1509-12. PubMed ID: 15505178
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The hereditary spinocerebellar ataxias in Japan.
    Sasaki H; Yabe I; Tashiro K
    Cytogenet Genome Res; 2003; 100(1-4):198-205. PubMed ID: 14526181
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Suppression of the yeast elongation factor Spt4 ortholog reduces expanded SCA36 GGCCUG repeat aggregation and cytotoxicity.
    Furuta N; Tsukagoshi S; Hirayanagi K; Ikeda Y
    Brain Res; 2019 May; 1711():29-40. PubMed ID: 30610877
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier?
    Matsuura T; Fang P; Pearson CE; Jayakar P; Ashizawa T; Roa BB; Nelson DL
    Am J Hum Genet; 2006 Jan; 78(1):125-9. PubMed ID: 16385455
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Post-zygotic de novo trinucleotide repeat expansion at spinocerebellar ataxia type 7 locus: evidence from an Indian family.
    Mittal U; Roy S; Jain S; Srivastava AK; Mukerji M
    J Hum Genet; 2005; 50(3):155-157. PubMed ID: 15750685
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Estimation of survival in spinocerebellar ataxia type 2 Cuban patients.
    Almaguer-Mederos LE; Aguilera Rodríguez R; González Zaldivar Y; Almaguer Gotay D; Cuello Almarales D; Laffita Mesa J; Vázquez Mojena Y; Zayas Feria P; Auburger G; Gispert S; Velásquez Pérez L
    Clin Genet; 2013 Mar; 83(3):293-4. PubMed ID: 22758789
    [No Abstract]   [Full Text] [Related]  

  • 18. Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestry.
    Bushara K; Bower M; Liu J; McFarland KN; Landrian I; Hutter D; Teive HA; Rasmussen A; Mulligan CJ; Ashizawa T
    PLoS One; 2013; 8(11):e81342. PubMed ID: 24278426
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Spinocerebellar ataxia type 10 in Peru: the missing link in the Amerindian origin of the disease.
    Leonardi L; Marcotulli C; McFarland KN; Tessa A; DiFabio R; Santorelli FM; Pierelli F; Ashizawa T; Casali C
    J Neurol; 2014 Sep; 261(9):1691-4. PubMed ID: 24935856
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Long-range PCR for the diagnosis of spinocerebellar ataxia type 10.
    Kurosaki T; Matsuura T; Ohno K; Ueda S
    Neurogenetics; 2008 May; 9(2):151-2. PubMed ID: 18197441
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.