(Q41924721)

14 October 2017

title

Pontocerebellar hypoplasia type 2 (PCH2): report of two siblings (English)

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14 October 2017

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Coppola G

1

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14 October 2017

Muras I

series ordinal

2

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14 October 2017

Pascotto A

series ordinal

3

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14 October 2017

publication date

1 May 2000

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14 October 2017

published in

Brain and Development

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14 October 2017

volume

22

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14 October 2017

issue

3

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14 October 2017

page(s)

188-192

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

14 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900093-0

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%2800%2900093-0

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%2FS0387-7604%2800%2900093-0

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%2FS0387-7604%2800%2900093-0

7 January 2021

Cerebellar hypoplasia associated with systemic degeneration in early life

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900093-0

7 January 2021

Hypoplasia ponto-neocerebellaris (author's transl)

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900093-0

7 January 2021

Ponto-cerebellar hypoplasia with dystonia: clinico-pathological findings in a sporadic case

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900093-0

7 January 2021

10.1016/S0387-7604(00)00093-0

Identifiers

DOI

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14 October 2017

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