Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patients - Wikidata - awgldk - TriplyDB

Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patients

Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patients

http://www.wikidata.org/entity/Q31120190

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CADASIL and CARASIL.Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: update on clinical, diagnostic, and management aspects.CADASIL: Ultrastructural insights into the morphology of granular osmiophilic material.Interpretation of NOTCH3 mutations in the diagnosis of CADASIL.Monogenic causes of stroke: now and the future.CADASIL: Treatment and Management Options.Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in Argentina.Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy.

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Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patients

http://www.wikidata.org/entity/Q31120190

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2013 nî lūn-bûn

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2013 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2013 թվականի հունիսին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patients

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Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patients

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Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patients

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Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patients

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Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patients

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Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patients

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JOURNAL.PONE.0065482

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Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patients

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Daniela Marzioni

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Elisabetta Cartechini

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Luigi Pianese

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Manrico Morroni

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Marina Scarpelli

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Mario Castellucci

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Michele Ragno

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Paolo Di Bella

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P2860

The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

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

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

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

The spectrum of Notch3 mutations in 28 Italian CADASIL families.

Renal involvement in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis.

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

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

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