(Q53207188)

English

Severity and progression rate of cerebellar ataxia in 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA) in the endemic Nagano Area of Japan.

scientific article published in March 2009

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

Severity and progression rate of cerebellar ataxia in 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA) in the endemic Nagano Area of Japan. (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

cerebellar ataxia

1 reference

based on heuristic

inferred from title

Katsuya Nakamura

8

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

13

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

author name string

Kunihiro Yoshida

1

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

Yusaku Shimizu

2

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

Hiroshi Morita

3

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

Tomomi Okano

4

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

Haruya Sakai

5

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

Takako Ohata

6

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

Naomichi Matsumoto

7

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

Ko-ichi Tazawa

9

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

Shinji Ohara

10

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

Kenichi Tabata

11

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

Atsushi Inoue

12

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

Yasuhiro Shimojima

14

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

Takeshi Hattori

15

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

Masao Ushiyama

16

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

Shu-ichi Ikeda

17

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

publication date

1 March 2009

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

8

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

1

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

46-51

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

https://scigraph.springernature.com/pub.10.1007/s12311-008-0062-8

0 references

Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional features of autosomal-dominant cerebellar ataxia in Nagano: clinical and molecular genetic analysis of 86 families

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dominant spinocerebellar ataxias: a molecular approach to classification, diagnosis, pathogenesis and the future

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Type I (transthyretin Met30) familial amyloid polyneuropathy in Japan: early- vs late-onset form

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Late-onset familial amyloid polyneuropathy type I (transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan. Clinicopathological and genetic features

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor dom

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inter-rater reliability of the International Cooperative Ataxia Rating Scale (ICARS).

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spinocerebellar ataxia type 6. Molecular and clinical features of 35 Japanese patients including one homozygous for the CAG repeat expansion

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Scale for the assessment and rating of ataxia: development of a new clinical scale

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and genetic epidemiological study of 16q22.1-linked autosomal dominant cerebellar ataxia in western Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical features and classification of inherited ataxias.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese families

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene on SCA4 locus causes dominantly inherited pure cerebellar ataxia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The hereditary spinocerebellar ataxias in Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18855094

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S12311-008-0062-8

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/18855094

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q53207188&oldid=1521576891"