Stroke in children: genetic and metabolic issues. - Wikidata - awgldk - TriplyDB

Stroke in children: genetic and metabolic issues.

Stroke in children: genetic and metabolic issues.

http://www.wikidata.org/entity/Q33929527

about

Pediatric stroke: a review Migrainous infarction: a rare and often overlooked diagnosis.Profile of pediatric hemiparesis.

P2860

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P2860

Stroke in children: genetic and metabolic issues.

http://www.wikidata.org/entity/Q33929527

description

2000 nî lūn-bûn

@nan

2000 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի մայիսին հրատարակված գիտական հոդված

@hy

2000年の論文

@ja

2000年論文

@yue

2000年論文

@zh-hant

2000年論文

@zh-hk

2000年論文

@zh-mo

2000年論文

@zh-tw

2000年论文

@wuu

name

Stroke in children: genetic and metabolic issues.

@ast

Stroke in children: genetic and metabolic issues.

@en

type

label

Stroke in children: genetic and metabolic issues.

@ast

Stroke in children: genetic and metabolic issues.

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prefLabel

Stroke in children: genetic and metabolic issues.

@ast

Stroke in children: genetic and metabolic issues.

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088307380001500507

P1433

Journal of Child Neurology

P1476

Stroke in children: genetic and metabolic issues.

@en

P2093

M G Bialer

http://www.w3.org/2001/XMLSchema#string

P B Kingsley

http://www.w3.org/2001/XMLSchema#string

S G Pavlakis

http://www.w3.org/2001/XMLSchema#string

P2860

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

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

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

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

Familial right ventricular dilated cardiomyopathy

Mendelian etiologies of stroke.

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

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

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

Defective molybdopterin biosynthesis: clinical heterogeneity associated with molybdenum cofactor deficiency.

P304

308-315

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P31

scholarly article

P356

10.1177/088307380001500507

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P433

5

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P478

15

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P577

2000-05-01T00:00:00Z

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P698

10830197

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