(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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Antithrombotic treatments, outcomes, and prognostic factors in acute childhood-onset arterial ischaemic stroke: a multicentre, observational, cohort study

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7 January 2021

Pediatric stroke in the United States and the impact of risk factors

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7 January 2021

The 5-year direct medical cost of neonatal and childhood stroke in a population-based cohort

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7 January 2021

Childhood Posterior Circulation Arterial Ischemic Stroke

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7 January 2021

Investigation of risk factors in children with arterial ischemic stroke

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7 January 2021

Clinical and radiological recurrence after childhood arterial ischemic stroke

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7 January 2021

Evolution of cerebral arteriopathies in childhood arterial ischemic stroke

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7 January 2021

Diagnosis and management of pediatric arterial ischemic stroke.

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7 January 2021

The association of CTLA-4 and CD28 gene polymorphisms with idiopathic ischemic stroke in the paediatric population.

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7 January 2021

Genetic polymorphisms of Chinese patients with ischemic stroke and concurrent stenoses of extracranial and intracranial vessels.

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7 January 2021

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

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7 January 2021

TNF-alpha -308G/A and IL-6 -174 G/C polymorphisms in the Turkish pediatric stroke patients

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7 January 2021

Genetic risk factors for arterial ischemic stroke in children: a possible MTHFR and eNOS gene-gene interplay?

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7 January 2021

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

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7 January 2021

Vascular development: genetic mechanisms and links to vascular disease

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7 January 2021

Inherited metabolic disorders and cerebral infarction.

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7 January 2021

COL4A1 mutations and hereditary angiopathy, nephropathy, aneurysms, and muscle cramps

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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

COL4A1 mutation in a patient with sporadic, recurrent intracerebral hemorrhage

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7 January 2021

Mutations in ABCC6 cause pseudoxanthoma elasticum

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7 January 2021

Pseudoxanthoma elasticum: molecular genetics and putative pathomechanisms

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7 January 2021

Pseudoxanthoma elasticum.

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https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Prevalence of symptomatic intracranial aneurysm and ischaemic stroke in pseudoxanthoma elasticum

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Cerebral arteriopathy in children with neurofibromatosis type 1.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Venous aneurysm, arterial dysplasia, and near-fatal hemorrhages in neurofibromatosis type 1

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https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

The vascular lesions of neurofibromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Williams-Beuren syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Stroke in Williams syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Ischemic stroke and intracranial multifocal cerebral arteriopathy in Williams syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

An autopsied case of Williams syndrome complicated by moyamoya disease

1 reference

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7 January 2021

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

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7 January 2021

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a genetic cause of cerebral small vessel disease

1 reference

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7 January 2021

An overview of Notch3 function in vascular smooth muscle cells

1 reference

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7 January 2021

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy resulting in stroke in an 11-year-old male.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

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7 January 2021

The prevalence of cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) in the west of Scotland

1 reference

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7 January 2021

Intracranial vascular abnormalities in patients with Alagille syndrome

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7 January 2021

Vascular anomalies in Alagille syndrome: a significant cause of morbidity and mortality

1 reference

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7 January 2021

Renovascular hypertension and vascular anomalies in Alagille syndrome

1 reference

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7 January 2021

Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease.

1 reference

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7 January 2021

Intracerebral large artery disease in Aicardi-Goutières syndrome implicates SAMHD1 in vascular homeostasis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Mutations in the pericentrin (PCNT) gene cause primordial dwarfism

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Molecular diagnosis of Menkes disease: genotype-phenotype correlation.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

1 reference

7 January 2021

Cerebral infarction in Menkes’ disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Ischemic stroke in an adolescent with arterial tortuosity syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Making sense of latent TGFbeta activation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Fabry disease - Vascular manifestations

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Cystathionine beta-synthase mutations in homocystinuria

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

1 reference

7 January 2021

Histopathology of the brain vascular network in moyamoya disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Human leukocyte antigen in patients with moyamoya disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Moyamoya disease: current concepts and future perspectives

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Familial occurrence of moyamoya disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Pathophysiology and genetic factors in moyamoya disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

A hereditary moyamoya syndrome with multisystemic manifestations.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

Role of COL4A1 in small-vessel disease and hemorrhagic stroke

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

The role of statins in the prevention of ischemic stroke

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970327-6

7 January 2021

10.1016/S1474-4422(10)70327-6

Identifiers

DOI

1 reference

24 August 2017

1 reference