(Q28255796)

9

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Marie-Germaine Bousser

10

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Anne Joutel

object named as

A Joutel

Elisabeth Tournier-Lasserve

1

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object named as

E Tournier-Lasserve

12

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author name string

K Vahedi

2

0 references

C Corpechot

3

0 references

A Troesch

4

0 references

H Chabriat

5

0 references

C Vayssière

6

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J Maciazek

8

0 references

J F Bach

Chronic familial vascular encephalopathy

11

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language of work or name

English

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publication date

22 November 1997

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published in

The Lancet

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volume

350

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page(s)

1511-5

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issue

9090

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cites work

1 reference

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7 January 2021

Hereditary multi-infarct dementia

1 reference

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

1 reference

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Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.

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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12

1 reference

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7 January 2021

Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study.

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Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

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7 January 2021

Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

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7 January 2021

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

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Specific truncations of Drosophila Notch define dominant activated and dominant negative forms of the receptor.

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Specific EGF repeats of Notch mediate interactions with Delta and serrate: Implications for notch as a multifunctional receptor

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7 January 2021

BRCA1Mutations in a Population-Based Sample of Young Women with Breast Cancer

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7 January 2021

Epidermal growth factor-like modules

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7 January 2021

Delta, a Drosophila neurogenic gene, is transcriptionally complex and encodes a protein related to blood coagulation factors and epidermal growth factor of vertebrates.

1 reference

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7 January 2021

The gene Serrate encodes a putative EGF-like transmembrane protein essential for proper ectodermal development in Drosophila melanogaster.

1 reference

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7 January 2021

Developmental signaling. Vertebrate ligands for Notch.

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Constitutive activation of fibroblast growth factor receptor-2 by a point mutation associated with Crouzon syndrome.

1 reference

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7 January 2021

Activation of RET as a dominant transforming gene by germline mutations of MEN2A and MEN2B

1 reference

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7 January 2021

Mutations altering the structure of epidermal growth factor-like coding sequences at the Drosophila Notch locus

1 reference

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7 January 2021

Cell-autonomous role of Notch, an epidermal growth factor homologue, in sensory organ differentiation in Drosophila

1 reference

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7 January 2021

10.1016/S0140-6736(97)08083-5

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1473408

1473408

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference