Fatal outcome in a case of pontocerebellar hypoplasia type 2. (Q41924384)

14 October 2017

title

Fatal outcome in a case of pontocerebellar hypoplasia type 2. (English)

1 reference

14 October 2017

Grellner W

1

1 reference

14 October 2017

Rohde K

series ordinal

2

1 reference

14 October 2017

Wilske J

series ordinal

3

1 reference

14 October 2017

publication date

1 September 2000

1 reference

Forensic Science International

14 October 2017

published in

1 reference

14 October 2017

volume

113

1 reference

14 October 2017

issue

1-3

1 reference

14 October 2017

page(s)

165-172

1 reference

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

14 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, and extrapyramidal dyskinesia (pontocerebellar hypoplasia type 2): compiled data from 10 pedigrees

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

Inherited syndrome of microcephaly, dyskinesia and pontocerebellar hypoplasia: a systemic atrophy with early onset

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

Genetic disorders and cerebellar structural abnormalities in childhood

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

MR findings in pontocerebellar hypoplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

Pontocerebellar hypoplasia with microcephaly and dyskinesia: report of two cases.

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

[Olivo-ponto-cerebral hypoplasia--case report of a neurodegenerative disease manifesting at birth with a fatal outcome]

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

Three siblings of fatal infantile encephalopathy with olivopontocerebellar hypoplasia and microcephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

Lissencephaly with pontocerebellar hypoplasia.

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

A syndrome of autosomal recessive pontocerebellar hypoplasia with white matter abnormalities and protracted course in two brothers

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

Familial infantile olivopontocerebellar atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

Congenital pontocerebellar atrophy in three patients: clinical, radiologic and etiologic considerations.

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

Congenital olivopontocerebellar atrophy: report of two siblings with paleo- and neocerebellar atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

Pontocerebellar hypoplasia associated with infantile motor neuron disease (Norman's disease).

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

Amyotrophic cerebellar hypoplasia: a specific form of infantile spinal atrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

Anterior horn cell disease associated with pontocerebellar hypoplasia in infants

1 reference

https://api.crossref.org/works/10.1016%2FS0379-0738%2800%2900270-X

7 January 2021

10.1016/S0379-0738(00)00270-X

Identifiers

DOI

1 reference

14 October 2017

1 reference