(Q41926344)

14 October 2017

Three siblings of fatal infantile encephalopathy with olivopontocerebellar hypoplasia and microcephaly (English)

1 reference

14 October 2017

0 references

1 reference

Hashimoto K

1

1 reference

14 October 2017

Takeuchi Y

2

1 reference

14 October 2017

Kida Y

3

1 reference

14 October 2017

Hasegawa H

4

1 reference

14 October 2017

Kantake M

5

1 reference

14 October 2017

Sasaki A

6

1 reference

14 October 2017

Asanuma K

7

1 reference

14 October 2017

Isumi H

8

1 reference

14 October 2017

Takashima S

9

1 reference

14 October 2017

1 April 1998

1 reference

14 October 2017

Brain and Development

1 reference

14 October 2017

20

1 reference

14 October 2017

3

1 reference

14 October 2017

169-174

1 reference

Fatal infantile encephalopathy with olivopontocerebellar hypoplasia and micrencephaly. Report of three siblings

14 October 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900014-X

7 January 2021

Hypoplasia ponto-neocerebellaris (author's transl)

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900014-X

7 January 2021

Congenital Spongy Degeneration of the Brain (Van Bogaert – Bertrand) Associated with Micrencephaly and Ponto – Cerebellar Atrophy (Contributions to the Pathology of Glial Dystrophy of Intrauterin Origin)

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900014-X

7 January 2021

Pontocerebellar hypoplasias. An overview of a group of inherited neurodegenerative disorders with fetal onset

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900014-X

7 January 2021

Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900014-X

7 January 2021

Familial olivopontocerebellar atrophy with neonatal onset: a recessively inherited syndrome with systemic and biochemical abnormalities.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900014-X

7 January 2021

Cerebellar hypoplasia associated with systemic degeneration in early life

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900014-X

7 January 2021

Disruption of the Hox-1.6 homeobox gene results in defects in a region corresponding to its rostral domain of expression

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900014-X

7 January 2021

Subtle Cerebellar Phenotype in Mice Homozygous for a Targeted Deletion of the En-2 Homeobox

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900014-X

7 January 2021

The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900014-X

7 January 2021

10.1016/S0387-7604(98)00014-X

Identifiers

DOI

1 reference

14 October 2017

1 reference