(Q44368315)

English

"CADASIL coma" in an Italian homozygous CADASIL patient: comparison with clinical and MRI findings in age-matched heterozygous patients with the same G528C NOTCH3 mutation

scientific article published on 10 April 2013

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

"CADASIL coma" in an Italian homozygous CADASIL patient: comparison with clinical and MRI findings in age-matched heterozygous patients with the same G528C NOTCH3 mutation (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

1 reference

based on heuristic

inferred from title

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based on heuristic

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based on heuristic

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Cristina Miceli

object named as

Cristina Miceli

8

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object named as

Marco Onofrj

10

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object named as

Luigi Trojano

11

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author name string

Michele Ragno

1

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Europe PubMed Central

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2 December 2017

Luigi Pianese

2

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Europe PubMed Central

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2 December 2017

Manrico Morroni

3

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Europe PubMed Central

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2 December 2017

Gabriella Cacchiò

4

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

Antonio Manca

5

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Europe PubMed Central

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2 December 2017

Fabio Di Marzio

6

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Europe PubMed Central

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2 December 2017

Serena Silvestri

7

1 reference

Europe PubMed Central

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2 December 2017

Maria Scarcella

9

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2 December 2017

publication date

10 April 2013

1 reference

Europe PubMed Central

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2 December 2017

Neurological Sciences

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Europe PubMed Central

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2 December 2017

34

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Europe PubMed Central

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2 December 2017

11

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2 December 2017

1947-1953

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Europe PubMed Central

PubMed publication ID

2 December 2017

https://scigraph.springernature.com/pub.10.1007/s10072-013-1418-5

0 references

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

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1418-5

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1418-5

21 January 2018

CADASIL: a monogenic condition causing stroke and subcortical vascular dementia

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1418-5

21 January 2018

Carotid atherosclerotic markers in CADASIL.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1418-5

21 January 2018

Neuromuscular implications in CADASIL.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1418-5

21 January 2018

Multi-organ investigation in 16 CADASIL families from central Italy sharing the same R1006C mutation.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1418-5

21 January 2018

Simultaneous impairment of intracranial and peripheral artery vasoreactivity in CADASIL patients.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1418-5

21 January 2018

"CADASIL coma": an underdiagnosed acute encephalopathy

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1418-5

21 January 2018

Clinical spectrum of CADASIL and the effect of cardiovascular risk factors on phenotype: study in 200 consecutively recruited individuals

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1418-5

21 January 2018

Interobserver agreement for the assessment of handicap in stroke patients.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1418-5

21 January 2018

A semiquantative rating scale for the assessment of signal hyperintensities on magnetic resonance imaging.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1418-5

21 January 2018

High recurrence of the R1006C NOTCH3 mutation in central Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1418-5

21 January 2018

Investigation of the single case in neuropsychology: confidence limits on the abnormality of test scores and test score differences.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1418-5

21 January 2018

Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASIL

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1418-5

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1418-5

21 January 2018

Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/23572112

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/23572112

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reversible coma with raised intracranial pressure: an unusual clinical manifestation of CADASIL

1 reference

https://pubmed.ncbi.nlm.nih.gov/23572112

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The International Classification of Headache Disorders: 2nd edition

1 reference

https://pubmed.ncbi.nlm.nih.gov/23572112

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygosity for a NOTCH3 mutation in a 65-year-old CADASIL patient with mild symptoms: a family report

1 reference

https://pubmed.ncbi.nlm.nih.gov/23572112

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal involvement in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): report of a case with a six-year follow-up.

1 reference

https://pubmed.ncbi.nlm.nih.gov/23572112

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The phenotypic spectrum of CADASIL: clinical findings in 102 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/23572112

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10072-013-1418-5

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

ResearchGate publication ID

0 references

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