HERNS. A rare, hereditary, multisystemic disease with cerebral microangiopathy (Q30988241)

28 June 2017

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title

HERNS. A rare, hereditary, multisystemic disease with cerebral microangiopathy (English)

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28 June 2017

Seifried C

1

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28 June 2017

Sitzer M

series ordinal

2

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28 June 2017

Jen J

series ordinal

3

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28 June 2017

Auburger G

series ordinal

4

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28 June 2017

language of work or name

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1 October 2005

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28 June 2017

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28 June 2017

volume

76

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28 June 2017

issue

10

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28 June 2017

page(s)

1191-2, 1194-5

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A new cause of hereditary small vessel disease: angiopathy of retina and brain

28 June 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00115-005-1910-0

Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00115-005-1910-0

The Ocular Manifestations in Fabry's Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00115-005-1910-0

Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00115-005-1910-0

Cerebroretinal vasculopathy mimicking a brain tumor: a case of a rare hereditary syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00115-005-1910-0

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00115-005-1910-0

Treatment of radiation-induced nervous system injury with heparin and warfarin

21 January 2018

1 reference

12 December 2020

Cerebroretinal vasculopathy and leukoencephalopathy mimicking a brain tumor. Report of two early-onset cases with Fanconi's anemia-like phenotypes suggesting an autosomal-recessive inheritance pattern.

1 reference

12 December 2020

Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3

1 reference

12 December 2020

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

1 reference

12 December 2020

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval

1 reference

12 December 2020

Cerebroretinal vasculopathy. A new hereditary syndrome

1 reference

12 December 2020

Hereditäre okklusive zerebroretinale Vaskulopathie bei zwei Schwestern12

1 reference

12 December 2020

10.1007/S00115-005-1910-0

Identifiers

DOI

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Dimensions Publication ID

28 June 2017

1005038655

0 references

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