(Q80778342)

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3 January 2020

title

Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 NOTCH3 gene mutation (English)

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3 January 2020

8

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3 January 2020

author name string

M Ragno

1

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3 January 2020

G Cacchiò

2

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3 January 2020

G M Fabrizi

3

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3 January 2020

M Scarcella

4

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3 January 2020

F Silvaggio

5

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3 January 2020

T Cavallaro

6

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3 January 2020

F Taioli

7

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3 January 2020

publication date

10 August 2007

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3 January 2020

published in

Neurological Sciences

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3 January 2020

volume

28

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3 January 2020

issue

4

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3 January 2020

page(s)

181-184

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

3 January 2020

cites work

1 reference

12 December 2020

A two-year clinical follow-up study in 80 CADASIL subjects: progression patterns and implications for clinical trials

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12 December 2020

CADASIL presenting as bipolar disorder.

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12 December 2020

CADASIL with a novel mutation in exon 7 of NOTCH3 (C388Y)

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12 December 2020

Diagnostic strategies in CADASIL

1 reference

12 December 2020

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: phenotypic and mutational spectrum

1 reference

12 December 2020

Spectrum of mutations in biopsy-proven CADASIL: implications for diagnostic strategies

1 reference

12 December 2020

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

1 reference

12 December 2020

Two novel Italian CADASIL families from Central Italy with mutation CGC-TGC at codon 1006 in the exon 19 Notch3 gene

1 reference

12 December 2020

The spectrum of mutations for CADASIL diagnosis

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12 December 2020

The spectrum of Notch3 mutations in 28 Italian CADASIL families

1 reference

12 December 2020

CADASIL: a common form of hereditary arteriopathy causing brain infarcts and dementia

1 reference

12 December 2020

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

1 reference

12 December 2020

CADASIL: neuropsychological findings in three generations of an affected family.

1 reference

12 December 2020

Cognitive profile in CADASIL patients

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12 December 2020

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

1 reference

12 December 2020

Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis

1 reference

12 December 2020

Diagnostic strategies in CADASIL

1 reference

12 December 2020

A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL.

1 reference

12 December 2020

Insidious cognitive decline in CADASIL.

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12 December 2020

Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study

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12 December 2020

10.1007/S10072-007-0817-X

Identifiers

DOI

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3 January 2020

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