(Q41562385)

3 October 2017

Prevalence of Fabry disease in dialysis patients: Japan Fabry disease screening study (J-FAST). (English)

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3 October 2017

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Osamu Saito

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3 October 2017

Eiji Kusano

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Tetsu Akimoto

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3 October 2017

Yasushi Asano

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3 October 2017

Teruo Kitagawa

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3 October 2017

Ken Suzuki

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3 October 2017

Nobuyuki Ishige

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3 October 2017

Takashi Akiba

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3 October 2017

Akira Saito

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3 October 2017

Eiji Ishimura

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3 October 2017

Motoshi Hattori

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3 October 2017

Akira Hishida

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3 October 2017

Chu Guili

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3 October 2017

Hiroki Maruyama

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3 October 2017

Masahisa Kobayashi

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3 October 2017

Touya Ohashi

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3 October 2017

Ichiro Matsuda

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3 October 2017

Yoshikatsu Eto

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3 October 2017

22 July 2015

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3 October 2017

10

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Clinical and experimental nephrology

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published in

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3 October 2017

20

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3 October 2017

284-293

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3 October 2017

2

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https://scigraph.springernature.com/pub.10.1007/s10157-015-1146-7

3 October 2017

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cites work

Fabry's Disease: Alpha-Galactosidase Deficiency

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Fabry disease peripheral blood immune cells release inflammatory cytokines: role of globotriaosylceramide

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Renal disease in Fabry patients

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Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10157-015-1146-7

alpha-Galactosidase A deficiency in Dutch patients on dialysis: a critical appraisal of screening for Fabry disease.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10157-015-1146-7

Significance of screening for Fabry disease among male dialysis patients

21 January 2018

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A nationwide blood spot screening study for Fabry disease in the Czech Republic haemodialysis patient population.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10157-015-1146-7

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

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10157-015-1146-7

Two-tier approach for the detection of alpha-galactosidase A deficiency in a predominantly female haemodialysis population.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10157-015-1146-7

Frequency of Fabry disease in male and female haemodialysis patients in Spain

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10157-015-1146-7

Screening of male dialysis patients for fabry disease by plasma globotriaosylsphingosine

21 January 2018

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Overview of regular dialysis treatment in Japan (as of 31 December 2009).

21 January 2018

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Non-invasive high-risk screening for Fabry disease hemizygotes and heterozygotes

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10157-015-1146-7

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

21 January 2018

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Anderson-Fabry disease: a multiorgan disease

21 January 2018

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Enzyme therapy in Fabry disease: differential in vivo plasma clearance and metabolic effectiveness of plasma and splenic alpha-galactosidase A isozymes

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10157-015-1146-7

Long-term outcome of enzyme-replacement therapy in advanced Fabry disease: evidence for disease progression towards serious complications

21 January 2018

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Consequences of a global enzyme shortage of agalsidase beta in adult Dutch Fabry patients

21 January 2018

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Enzyme replacement therapy for Fabry disease: lessons from two alpha-galactosidase A orphan products and one FDA approval

21 January 2018

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Diagnosis of Fabry disease: usefulness of the clinical investigation

21 January 2018

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Newborn screening for Fabry disease in Japan: prevalence and genotypes of Fabry disease in a pilot study

21 January 2018

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12 December 2020

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

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12 December 2020

Fabry disease in patients with end-stage renal failure: the potential benefits of screening

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12 December 2020

Results of a nationwide screening for Anderson-Fabry disease among dialysis patients

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12 December 2020

Fabry disease: detection of undiagnosed hemodialysis patients and identification of a "renal variant" phenotype

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12 December 2020

No accumulation of globotriaosylceramide in the heart of a patient with the E66Q mutation in the α-galactosidase A gene

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12 December 2020

Identification of Fabry's disease by the screening of alpha-galactosidase A activity in male and female hemodialysis patients.

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12 December 2020

Identification of a novel mutation and prevalence study for fabry disease in Japanese dialysis patients

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12 December 2020

Replacement Therapy for Inherited Enzyme Deficiency

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12 December 2020

High-throughput screening identified disease-causing mutants and functional variants of α-galactosidase A gene in Japanese male hemodialysis patients

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12 December 2020

Fabry disease in hemodialysis patients in southern Brazil: prevalence study and clinical report

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12 December 2020

Fabry's disease: enzymatic diagnosis of hemizygotes and heterozygotes. Alpha-galactosidase activities in plasma, serum, urine, and leukocytes

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12 December 2020

Enzyme replacement therapy for Fabry's disease

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12 December 2020

Differential assay for lysosomal alpha-galactosidases in human tissues and its application to Fabry's disease

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12 December 2020

10.1007/S10157-015-1146-7

Identifiers

DOI

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3 October 2017

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