(Q33929527)

30 July 2017

1 reference

title

Stroke in children: genetic and metabolic issues (English)

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30 July 2017

S G Pavlakis

1

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30 July 2017

P B Kingsley

series ordinal

2

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30 July 2017

M G Bialer

series ordinal

3

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30 July 2017

language of work or name

1 reference

1 May 2000

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Journal of Child Neurology

30 July 2017

published in

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30 July 2017

volume

15

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30 July 2017

issue

5

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30 July 2017

page(s)

308-315

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Mendelian etiologies of stroke

30 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current concepts

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Familial right ventricular dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

21 January 2018

Familial Atrial Myxoma

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Gorlin's syndrome and the heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Functional methionine synthase deficiency due to cblG disorder: a report of two patients and a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Stroke in Fabry's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Protein C and protein S activity in sickle cell disease and stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Alpha thalassemia and stroke risk in sickle cell anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Hypertensive encephalopathy, reversible occipitoparietal encephalopathy, or reversible posterior leukoencephalopathy: three names for an old syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Prothrombotic disorders in infants and children with cerebral thromboembolism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Prethrombotic disorders in children with arterial ischemic stroke and sinovenous thrombosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Epidemiological features of moyamoya disease in Japan: findings from a nationwide survey.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Metabolic stroke in carbamyl phosphate synthetase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Cerebellar hemorrhage complicating methylmalonic and propionic acidemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Acute basal ganglia infarction in propionic acidemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Atypical presentation and neuropathological studies in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Stroke-like encephalopathy in an infant with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Acute hemiparesis as the presenting sign in a heterozygote for ornithine transcarbamylase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Magnetic resonance spectroscopy: use in monitoring MELAS treatment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Sulfite oxidase deficiency. Biochemical and clinical investigations of a hereditary metabolic disorder in sulfur metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Defective molybdopterin biosynthesis: clinical heterogeneity associated with molybdenum cofactor deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Stroke in purine nucleoside phosphorylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Alternating hemiplegia in childhood: a cross-sectional study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

Preventing Coronary Heart Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500507

10.1177/088307380001500507

21 January 2018

Identifiers

DOI

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30 July 2017

1 reference