Paediatric stroke: genetic insights into disease mechanisms and treatment targets (Q37846935)

24 August 2017

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title

Paediatric stroke: genetic insights into disease mechanisms and treatment targets (English)

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24 August 2017

Yanick J Crow

2

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author name string

Pinki Munot

series ordinal

1

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24 August 2017

Vijeya Ganesan

series ordinal

3

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24 August 2017

publication date

1 March 2011

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24 August 2017

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24 August 2017

volume

10

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24 August 2017

issue

3

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24 August 2017

page(s)

264-274

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Risk of stroke in children: ethnic and gender disparities.

24 August 2017

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Candidate gene polymorphisms do not differ between newborns with stroke and normal controls.

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7 January 2021

A dominantly inherited mutation in collagen IV A1 (COL4A1) causing childhood onset stroke without porencephaly.

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7 January 2021

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7 January 2021

Prevalence of symptomatic intracranial aneurysm and ischaemic stroke in pseudoxanthoma elasticum

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7 January 2021

Elastosis perforans serpiginosa-like pseudoxanthoma elasticum in a child with severe Moya Moya disease.

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7 January 2021

Genetic variants promoting smooth muscle cell proliferation can result in diffuse and diverse vascular diseases: evidence for a hyperplastic vasculomyopathy

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7 January 2021

Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease

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7 January 2021

De novo ACTA2 mutation causes a novel syndrome of multisystemic smooth muscle dysfunction

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7 January 2021

ACTA2 is not a major disease-causing gene for moyamoya disease

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7 January 2021

Molecular targets for emerging anti-tumor therapies for neurofibromatosis type 1.

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7 January 2021

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7 January 2021

The vascular lesions of neurofibromatosis

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7 January 2021

Genetic and cellular evidence of vascular inflammation in neurofibromin-deficient mice and humans

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7 January 2021

Nf1+/- mice have increased neointima formation via hyperactivation of a Gleevec sensitive molecular pathway

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7 January 2021

Williams-Beuren syndrome.

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7 January 2021

Stroke in Williams syndrome

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7 January 2021

Ischemic stroke and intracranial multifocal cerebral arteriopathy in Williams syndrome

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7 January 2021

An autopsied case of Williams syndrome complicated by moyamoya disease

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7 January 2021

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7 January 2021

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7 January 2021

An overview of Notch3 function in vascular smooth muscle cells

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7 January 2021

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7 January 2021

Childhood-onset CADASIL: clinical, imaging, and neurocognitive features

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Cerebral arterial stenoses and stroke: novel features of Aicardi-Goutières syndrome caused by the Arg164X mutation in SAMHD1 are associated with altered cytokine expression

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7 January 2021

Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response

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7 January 2021

Mutations in the pericentrin (PCNT) gene cause primordial dwarfism

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7 January 2021

Majewski osteodysplastic primordial dwarfism type II (MOPD II): expanding the vascular phenotype

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7 January 2021

A Novel Role for the Centrosomal Protein, Pericentrin, in Regulation of Insulin Secretory Vesicle Docking in Mouse Pancreatic β-cells

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7 January 2021

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7 January 2021

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7 January 2021

Cerebral infarction in Menkes’ disease

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7 January 2021

Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome

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7 January 2021

Ischemic stroke in an adolescent with arterial tortuosity syndrome

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7 January 2021

Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome

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7 January 2021

Glucose transporter 10 and arterial tortuosity syndrome: the vitamin C connection

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7 January 2021

Making sense of latent TGFbeta activation

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7 January 2021

Fabry disease - Vascular manifestations

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7 January 2021

Mutations of the GLA gene in young patients with stroke: the PORTYSTROKE study--screening genetic conditions in Portuguese young stroke patients

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7 January 2021

Cystathionine beta-synthase mutations in homocystinuria

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7 January 2021

Stroke in young patients with hyperhomocysteinemia due to cystathionine beta-synthase deficiency

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7 January 2021

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7 January 2021

Histopathology of the brain vascular network in moyamoya disease

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7 January 2021

Smooth muscle cell proliferation and localization of macrophages and T cells in the occlusive intracranial major arteries in moyamoya disease

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7 January 2021

Associations of Moyamoya patients with HLA class I and class II alleles in the Korean population

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7 January 2021

Human leukocyte antigen in patients with moyamoya disease

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7 January 2021

Analysis of class II genes of human leukocyte antigen in patients with moyamoya disease

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7 January 2021

Diffuse and uncontrolled vascular smooth muscle cell proliferation in rapidly progressing pediatric moyamoya disease

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7 January 2021

Moyamoya disease: current concepts and future perspectives

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7 January 2021

Familial occurrence of moyamoya disease

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7 January 2021

Autosomal dominant moyamoya disease maps to chromosome 17q25.3.

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7 January 2021

Pathophysiology and genetic factors in moyamoya disease

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7 January 2021

A hereditary moyamoya syndrome with multisystemic manifestations.

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7 January 2021

Role of COL4A1 in small-vessel disease and hemorrhagic stroke

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7 January 2021

Biomarkers of hypercoagulability and inflammation in childhood-onset arterial ischemic stroke.

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7 January 2021

Risk of recurrent childhood arterial ischemic stroke in a population-based cohort: the importance of cerebrovascular imaging

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7 January 2021

Predictors of cerebral arteriopathy in children with arterial ischemic stroke: results of the International Pediatric Stroke Study

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7 January 2021

Endothelial response to childhood infection: The role of mannose-binding lectin (MBL)

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7 January 2021

Varicella zoster virus vasculopathies: diverse clinical manifestations, laboratory features, pathogenesis, and treatment

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7 January 2021

The role of statins in the prevention of ischemic stroke

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7 January 2021

10.1016/S1474-4422(10)70327-6

Identifiers

DOI

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24 August 2017

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