(Q36012553)

11 August 2017

0 references

Familial hypertrophic obstructive cardiomyopathy with the GLA E66Q mutation and zebra body (English)

1 reference

hypertrophic obstructive cardiomyopathy

11 August 2017

0 references

8

Hitoshi Suzuki

1 reference

11 August 2017

Masayoshi Oikawa

1

1 reference

11 August 2017

Nobuo Sakamoto

2

1 reference

11 August 2017

Atsushi Kobayashi

3

1 reference

11 August 2017

Satoshi Suzuki

4

1 reference

11 August 2017

Akiomi Yoshihisa

5

1 reference

11 August 2017

Takayoshi Yamaki

6

1 reference

11 August 2017

Kazuhiko Nakazato

7

1 reference

11 August 2017

Shu-Ichi Saitoh

9

1 reference

11 August 2017

Yuichirou Kiko

10

1 reference

11 August 2017

Hajime Nakano

11

1 reference

11 August 2017

Takeharu Hayashi

12

1 reference

11 August 2017

Akinori Kimura

13

1 reference

11 August 2017

Yasuchika Takeishi

14

1 reference

11 August 2017

language of work or name

1 reference

10 May 2016

1 reference

BMC Cardiovascular Disorders

11 August 2017

1 reference

11 August 2017

16

1 reference

11 August 2017

83

1 reference

https://scigraph.springernature.com/pub.10.1186/s12872-016-0262-y

11 August 2017

0 references

cites work

Molecular genetics and pathogenesis of cardiomyopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4862085

Anderson-Fabry disease and other lysosomal storage disorders

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4862085

The frequency of Fabry disease with the E66Q variant in the α-galactosidase A gene in Japanese dialysis patients: a case report and a literature review

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4862085

Drug-induced phospholipidosis: are there functional consequences?

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4862085

Point mutations in the upstream region of the ?-galactosidase A gene exon 6 in an atypical variant of Fabry disease

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4862085

Chloroquine-induced lipidosis mimicking Fabry disease

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4862085

Role of the p.E66Q variant of GLA in the progression of chronic kidney disease

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4862085

p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small-vessel occlusion in elderly Japanese males

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4862085

Fabry disease: biochemical, pathological and structural studies of the α-galactosidase A with E66Q amino acid substitution.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4862085

Mutations of the GLA gene in Korean patients with Fabry disease and frequency of the E66Q allele as a functional variant in Korean newborns.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4862085

Prevalence and cardiovascular features of Japanese hemodialysis patients with Fabry disease.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4862085

Progressive renal insufficiency associated with amiodarone-induced phospholipidosis

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4862085

Prevalence and distribution of sarcomeric gene mutations in Japanese patients with familial hypertrophic cardiomyopathy

23 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27160240

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/S12872-016-0262-Y

1 reference

Dimensions Publication ID

11 August 2017

0 references

1 reference

11 August 2017

1 reference