(Q48106115)

English

Congenital pontocerebellar atrophy and telencephalic defects in three siblings: a new subtype

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17628812

Congenital pontocerebellar atrophy and telencephalic defects in three siblings: a new subtype (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17628812

1 reference

based on heuristic

inferred from title

4

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17628812

author name string

Jules G Leroy

1

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17628812

Gilles Lyon

2

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17628812

Catherine Fallet

3

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17628812

Claudine De Praeter

5

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17628812

Caroline Van Den Broecke

6

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17628812

Piet Vanhaesebrouck

7

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17628812

publication date

13 July 2007

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17628812

Acta Neuropathologica

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17628812

114

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17628812

4

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17628812

387-399

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17628812

https://scigraph.springernature.com/pub.10.1007/s00401-007-0248-z

0 references

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/10.1007%2FS00401-007-0248-Z

21 January 2018

CEREBELLO-THALAMO-SPINAL DEGENERATION IN INFANCY: AN UNUSUAL VARIANT OF WERDNIG-HOFFMANN DISEASE.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-007-0248-Z

21 January 2018

A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-007-0248-Z

21 January 2018

Identifiers

10.1007/S00401-007-0248-Z

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17628812

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17628812

ResearchGate publication ID

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