(Q28268718)

4

0 references

Anne Joutel

object named as

A Joutel

Elisabeth Tournier-Lasserve

2

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object named as

E Tournier-Lasserve

1

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Mark Lathrop

5

object named as

G M Lathrop

0 references

author name string

J Melki

3

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H Chabriat

6

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J L Mas

7

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E A Cabanis

8

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M Baudrimont

9

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J Maciazek

Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy

10

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language of work or name

English

0 references

publication date

March 1993

0 references

published in

Nature Genetics

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volume

3

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issue

3

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page(s)

256-9

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cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-256

A familial disorder with subcortical ischemic strokes, dementia, and leukoencephalopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-256

A second-generation linkage map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-256

Criteria for the diagnosis of ischemic vascular dementia proposed by the State of California Alzheimer's Disease Diagnostic and Treatment Centers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-256

Cerebral blood flow in dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-256

Infarcts of undetermined cause: the NINCDS Stroke Data Bank

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-256

7 January 2021

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-256

7 January 2021

Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-256

7 January 2021

Chronic familial vascular encephalopathy

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-256

7 January 2021

Hereditary multi-infarct dementia

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-256

7 January 2021

Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-256

7 January 2021

Slowly progressive familial dementia with recurrent strokes and white matter hypodensities on CT scan

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-256

7 January 2021

Amyloid beta protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch)

1 reference

https://api.crossref.org/works/10.1038%2FNG0393-256

7 January 2021