(Q45236280)

11 December 2017

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

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11 December 2017

K Nakamura

1

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11 December 2017

Y Sekijima

2

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11 December 2017

K Nakamura

3

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11 December 2017

K Hattori

4

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11 December 2017

K Nagamatsu

5

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11 December 2017

Y Shimizu

6

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11 December 2017

M Yazaki

7

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11 December 2017

A Sakurai

8

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11 December 2017

F Endo

9

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11 December 2017

Y Fukushima

10

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11 December 2017

S-I Ikeda

11

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11 December 2017

language of work or name

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31 May 2013

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European Journal of Neurology

11 December 2017

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11 December 2017

21

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11 December 2017

1

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11 December 2017

49-56

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Cerebrovascular complications of Fabry's disease

11 December 2017

1 reference

Central nervous system involvement in Anderson-Fabry disease: a clinical and MRI retrospective study.

21 January 2018

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Stroke in Fabry disease frequently occurs before diagnosis and in the absence of other clinical events: natural history data from the Fabry Registry

21 January 2018

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Prevalence of lysosomal storage disorders

21 January 2018

1 reference

Newborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset GLA mutation c.936+919G>A (IVS4+919G>A).

21 January 2018

1 reference

High incidence of later-onset fabry disease revealed by newborn screening

21 January 2018

1 reference

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

21 January 2018

1 reference

Prevalence of Anderson-Fabry disease in male patients with late onset hypertrophic cardiomyopathy

21 January 2018

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Prevalence of Fabry disease in patients with cryptogenic stroke: a prospective study.

21 January 2018

1 reference

Frequency of unrecognized Fabry disease among young European-American and African-American men with first ischemic stroke

21 January 2018

1 reference

Mutations of the GLA gene in young patients with stroke: the PORTYSTROKE study--screening genetic conditions in Portuguese young stroke patients

21 January 2018

1 reference

Belgian Fabry study: prevalence of Fabry disease in a cohort of 1000 young patients with cerebrovascular disease.

21 January 2018

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Acute cerebrovascular disease in the young: the Stroke in Young Fabry Patients study

21 January 2018

1 reference

Zurich Fabry study - prevalence of Fabry disease in young patients with first cryptogenic ischaemic stroke or TIA.

21 January 2018

1 reference

Fabry disease in unselected patients with TIA or stroke: population-based study.

21 January 2018

1 reference

Fabry's disease--an important risk factor for stroke.

21 January 2018

1 reference

Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment

21 January 2018

1 reference

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

21 January 2018

1 reference

Novel mutations of the GLA gene in Japanese patients with Fabry disease and their functional characterization by active site specific chaperone.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

1 reference

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

21 January 2018

1 reference

Quantitative analysis of cerebral vasculopathy in patients with Fabry disease.

21 January 2018

1 reference

The cerebral vasculopathy of Fabry disease.

21 January 2018

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21 January 2018

Identifiers

DOI

10.1111/ENE.12214

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11 December 2017

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