(Q51986799)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10073437%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

title

Congenital hydranencephalic-hydrocephalic syndrome associated with mitochondrial dysfunction (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10073437%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10073437%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

author name string

M Castro-Gago

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10073437%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

A Alonso

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10073437%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

E Pintos-Martínez

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10073437%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

A Beiras-Iglesias

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10073437%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

Y Campos

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10073437%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

M I Novo-Rodríguez

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10073437%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

J Eirís-Puñal

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10073437%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

publication date

1 February 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10073437%20AND%20SRC:MED&resulttype=core&format=json

Journal of Child Neurology

11 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10073437%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

volume

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10073437%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10073437%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

page(s)

131-135

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10073437%20AND%20SRC:MED&resulttype=core&format=json

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

11 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400213

Autosomal recessive hydrocephalus with aqueductal stenosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400213

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%2F088307389901400213

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%2F088307389901400213

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%2F088307389901400213

Autopsy findings in pyruvate dehydrogenase E1alpha deficiency: case report.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400213

Cytochrome c oxidase deficiency in Leigh syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400213

Pyruvate dehydrogenase complex activity in normal and deficient fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400213

Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the E1 alpha subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400213

Pyruvate dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400213

Mitochondrial angiopathy in a family with MELAS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389901400213

10.1177/088307389901400213

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10073437%20AND%20SRC:MED&resulttype=core&format=json

release_z6pu7fzcyrdvbj7yicwyi2g2vi

11 November 2019

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/z6pu7fzcyrdvbj7yicwyi2g2vi

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference