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THAP11 CAG Repeat Expansion Is Rare or Absent in the Taiwanese Cohort with Cerebellar Ataxia.

• Authors : Hsiao CT; Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan.; Department of Neurology, National Yang Ming Chiao Tung University School of Medicine, Taipei, Taiwan.

Subjects: Cerebellar Ataxia*/Cerebellar Ataxia*/Cerebellar Ataxia*/genetics ; Trinucleotide Repeat Expansion*/Trinucleotide Repeat Expansion*/Trinucleotide Repeat Expansion*/genetics; Humans

• Source: Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2024 May; Vol. 39 (5), pp. 924-925.Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print Cited Medium: Internet ISSN: 1531-8257

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Investigating PUM1 mutations in a Taiwanese cohort with cerebellar ataxia.

• Authors : Lai KL; Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan; Department of Neurology, National Yang-Ming University School of Medicine, Taipei, Taiwan

Subjects: Cerebellar Ataxia/Cerebellar Ataxia/Cerebellar Ataxia/*genetics ; RNA-Binding Proteins/RNA-Binding Proteins/RNA-Binding Proteins/*genetics; Adult

• Source: Parkinsonism & related disorders [Parkinsonism Relat Disord] 2019 Sep; Vol. 66, pp. 220-223. Date of Electronic Publication: 2019 Aug 07.Publisher: Elsevier Science Country of Publication: England NLM ID: 9513583 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Clinical and Genetic Characterization of Autosomal Recessive Spinocerebellar Ataxia Type 16 (SCAR16) in Taiwan.

• Authors : Chiu HH; Department of Neurology, Taipei Veterans General Hospital, Taipei, Taiwan.; Department of Neurology, National Yang-Ming University School of Medicine, Taipei, Taiwan.

Subjects: Cerebellar Ataxia/Cerebellar Ataxia/Cerebellar Ataxia/*genetics ; Gonadotropin-Releasing Hormone/Gonadotropin-Releasing Hormone/Gonadotropin-Releasing Hormone/*deficiency ; Hypogonadism/Hypogonadism/Hypogonadism/*genetics Cerebellar Ataxia and Hypogonadotropic Hypogonadism

• Source: Cerebellum (London, England) [Cerebellum] 2020 Aug; Vol. 19 (4), pp. 544-549.Publisher: Springer Country of Publication: United States NLM ID: 101089443 Publication Model: Print Cited Medium: Internet ISSN: 1473-4230

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Identification of m.3243A>G mitochondrial DNA mutation in patients with cerebellar ataxia.

• Authors : Liao, Nai-Yi; Lai, Kuan-Lin; Liao, Yi-Chu

Subjects: MELAS syndrome; CEREBELLAR ataxia; MITOCHONDRIAL DNATAIWAN

• Source: Journal of the Formosan Medical Association; Oct2023, Vol. 122 Issue 10, p1028-1034, 7p

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Nationwide population-based epidemiologic study on cerebellar ataxia in Taiwan.

• Authors : Tsai TL; Department of Neurology, Changhua Christian Hospital Lukang Branch, Changhua, Taiwan, ROC.; Liu CS

Subjects: Community Health Planning*; Cerebellar Ataxia/Cerebellar Ataxia/Cerebellar Ataxia/*epidemiology; Adolescent

• Source: European neurology [Eur Neurol] 2011; Vol. 66 (4), pp. 215-9. Date of Electronic Publication: 2011 Sep 21.Publisher: Karger Country of Publication: Switzerland NLM ID: 0150760 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1421-9913

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Gluten sensitivity: associated sporadic cerebellar ataxia in Taiwan.

• Authors : Liu CS; Department of Neurology, Vascular and Genomics Center, Changhua Christian Hospital, No. 135, Nanhsiao Street, Changhua 500, Taiwan. ; Soong BW

Subjects: Autoantibodies/Autoantibodies/Autoantibodies/*blood ; Cerebellar Ataxia/Cerebellar Ataxia/Cerebellar Ataxia/*immunology ; Gliadin/Gliadin/Gliadin/*immunology

• Source: Acta neurologica Taiwanica [Acta Neurol Taiwan] 2010 Dec; Vol. 19 (4), pp. 263-9.Publisher: Color Design Country of Publication: China (Republic : 1949- ) NLM ID: 9815355 Publication Model: Print Cited Medium: Print ISSN:

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Findings from Taipei Veterans General Hospital Has Provided New Data on Cerebellar Ataxia (Investigating itm2b-associated Ataxia In a Taiwanese Cerebellar Ataxia Cohort).

• Source: Mental Health Weekly Digest. December 30, 2024, 260.

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Frequency analysis of autosomal dominant cerebellar ataxias in Taiwanese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.

• Authors : Soong B W; Department of Neurology, National Yang-Ming University School of Medicine, Taipei, Taiwan, Republic of China. ; Lu Y C

Subjects: Founder Effect*; Cerebellar Ataxia/Cerebellar Ataxia/Cerebellar Ataxia/*genetics ; Genes, Dominant/Genes, Dominant/Genes, Dominant/*genetics

• Source: Archives of neurology [Arch Neurol] 2001 Jul; Vol. 58 (7), pp. 1105-9.Publisher: American Medical Assn Country of Publication: United States NLM ID: 0372436 Publication Model: Print Cited Medium: Print ISSN:

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A Novel SETX Mutation in a Taiwanese Patient with Autosomal Recessive Cerebellar Ataxia Detected by Targeted Next-Generation Sequencing, and a Literature Review.

• Authors : Chiang, Ping-I¹ (AUTHOR) ; Liao, Ting-Wei² (AUTHOR) ; Chen, Chiung-Mei^2,3 (AUTHOR)

Subjects: *SPINOCEREBELLAR ataxia; *CEREBELLAR ataxia; *NUCLEOTIDE sequencingTAIWAN; SAUDI Arabia

• Source: Brain Sciences (2076-3425). Feb2022, Vol. 12 Issue 2, p173. 1p.

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Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of Taiwan.

• Authors : Tsai, H.-F.^1,2; Liu, C.-S.^3,4; Leu, T.-M.⁵

Subjects: *TRINUCLEOTIDE repeats; *CEREBELLAR ataxia; *POLYMERASE chain reactionTAIWAN

• Source: Acta Neurologica Scandinavica. May2004, Vol. 109 Issue 5, p355-360. 6p.

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