(Q48180963)

English

4H syndrome: a rare cause of leukodystrophy.

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

4H syndrome: a rare cause of leukodystrophy. (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

2

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

author name string

Olivier Outteryck

1

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

Patrice Jissendi

3

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

Odile Boespflug-Tanguy

4

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

Lucie Hopes

5

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

Dimitri Renard

6

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

Joël Ferri

7

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

Patrick Vermersch

8

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

Pierre Labauge

9

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

publication date

30 May 2010

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

Journal of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

257

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

10

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

1759-1761

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

https://scigraph.springernature.com/pub.10.1007/s00415-010-5598-0

0 references

Leukoencephalopathy with ataxia, hypodontia, and hypomyelination.

1 reference

https://api.crossref.org/works/10.1007%2FS00415-010-5598-0

21 January 2018

Peripheral and central hypomyelination with hypogonadotropic hypogonadism and hypodontia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20512583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Leukodystrophy associated with oligodontia in a large inbred family: fortuitous association or new entity?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20512583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diffuse cerebral hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20512583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Central hypomyelination, hypogonadotrophic hypogonadism and hypodontia: a new leukodystrophy]

1 reference

https://pubmed.ncbi.nlm.nih.gov/20512583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypomyelination, hypogonadotropic hypogonadism, hypodontia - First Polish patient.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20512583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00415-010-5598-0

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/20512583

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