(Q48696636)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11732774%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

title

Congenital hydranencephalic-hydrocephalic syndrome with proliferative vasculopathy: a possible relation with mitochondrial dysfunction (English)

1 reference

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4 December 2019

10

1 reference

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4 December 2019

author name string

M Castro-Gago

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11732774%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

E Pintos-Martínez

2

1 reference

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4 December 2019

J Forteza-Vila

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11732774%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

M Iglesias-Diz

4

1 reference

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4 December 2019

R Ucieda-Somoza

5

1 reference

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4 December 2019

I Silva-Villar

6

1 reference

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4 December 2019

J Codesido-López

7

1 reference

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4 December 2019

A Viso-Lorenzo

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11732774%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

Y Campos

9

1 reference

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4 December 2019

J Eirís-Puñal

11

1 reference

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4 December 2019

publication date

1 November 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11732774%20AND%20SRC:MED&resulttype=core&format=json

Journal of Child Neurology

4 December 2019

published in

1 reference

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4 December 2019

volume

16

1 reference

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4 December 2019

issue

11

1 reference

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4 December 2019

page(s)

858-862

1 reference

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"Infantile hydranencephaly"--a report of five cases of infarction of both cerebral hemispheres in infancy.

4 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1177%2F08830738010160111401

The familial syndrome of proliferative vasculopathy and hydranencephaly-hydrocephaly: immunocytochemical and ultrastructural evidence for endothelial proliferation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738010160111401

Autosomal recessive hydrocephalus with aqueductal stenosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738010160111401

Lethal neonatal deficiency of carnitine palmitoyltransferase II associated with dysgenesis of the brain and kidneys.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738010160111401

Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers. II. Morphology and pathogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738010160111401

Cerebral dysgenesis and lactic acidemia: an MRI/MRS phenotype associated with pyruvate dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738010160111401

Autopsy findings in pyruvate dehydrogenase E1alpha deficiency: case report.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738010160111401

Congenital hydranencephalic-hydrocephalic syndrome associated with mitochondrial dysfunction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738010160111401

Diffuse meningocerebral angiodysplasia and renal agenesis: a case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738010160111401

Mitochondrial angiopathy in a family with MELAS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738010160111401

10.1177/08830738010160111401

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11732774%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

1 reference