(Q28251354)

22 April 2017

author name string

D Guidetti

1

0 references

B Casali

2

0 references

R L Mazzei

3

0 references

M T Dotti

4

0 references

D. Guidetti

1

1 reference

22 April 2017

B. Casali

2

1 reference

22 April 2017

R.L. Mazzei

3

1 reference

22 April 2017

M.T. Dotti

4

1 reference

22 April 2017

language of work or name

English

0 references

publication date

2006

1 reference

PubMed

January 2006

1 reference

Clinical and Experimental Hypertension

22 April 2017

published in

1 reference

22 April 2017

volume

28

1 reference

22 April 2017

issue

3-4

1 reference

22 April 2017

page(s)

271-277

1 reference

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

22 April 2017

cites work

2 references

https://api.crossref.org/works/10.1080%2F10641960600549223

22 April 2017

https://api.crossref.org/works/10.1080/10641960600549223

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

22 April 2017

2 references

https://api.crossref.org/works/10.1080%2F10641960600549223

22 April 2017

https://api.crossref.org/works/10.1080/10641960600549223

A Novel Mutation in the Notch3 Gene in an Italian Family With Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy

22 April 2017

1 reference

https://api.crossref.org/works/10.1080%2F10641960600549223

Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.

23 May 2017

1 reference

https://api.crossref.org/works/10.1080%2F10641960600549223

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10641960600549223

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10641960600549223

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10641960600549223

CADASIL: a review with proposed diagnostic criteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10641960600549223

Brain stem MRI signal abnormalities in CADASIL.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10641960600549223

A kindred affected by cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). A 2-year neuropsychological follow-up.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10641960600549223

Correlations between clinical findings and magnetization transfer imaging metrics of tissue damage in individuals with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10641960600549223

Early visual function impairment in CADASIL.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10641960600549223

Yield of screening for CADASIL mutations in lacunar stroke and leukoaraiosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10641960600549223

Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10641960600549223

An Italian case of CADASIL with mutation CGC-TCG in codon 1006, exon 19 Notch3 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10641960600549223

10.1080/10641960600549223

21 January 2018

Identifiers

DOI

1 reference