MMG PUBLICATIONS

Use the tool below to browse our publications by keywords or/and by team or/and by year.

Follow then the link to consult a publication on PUBMED website.



Search publications





Results: 4167  publications found.

L., .  et al. 0

C.; Cardoso

spastic paraplegia and skewed pattern of X inactivation;;;;;;;eng;;;;;PubMed;;PMID: 10417298 PMCID: PMC1377954
- issue: - volume: - pages: .

hypotonia, .  et al. 0

functional gastrointestinal abnormalities

- issue: - volume: - pages: .

this study, .  et al. 0

through secretomic analysis

- issue: - volume: - pages: .

M., .  et al. 0

P.; Villard

- issue: - volume: - pages: .

Proud V, .  et al. 0

Chiaroni P

- issue: - volume: - pages: .

Epilepsia. 2024 May, .  et al. 0

Cetica V

10.1111/epi.17939
- issue: - volume: - pages: .

A. M., .  et al. 0

M.; Colleaux

- issue: - volume: - pages: .

, .  et al. 0

- issue: - volume: - pages: .

p.(Thr493Asn) and p.(Gly496Arg), .  et al. 0

were located in the transmembrane domains S3 and S6 of Kv10.1 and one

- issue: - volume: - pages: .

Al Aqeel AI, .  et al. 0

Alhashem A

Doummar D
Issa MY - issue: Keren B - volume: Kuechler A - pages: Horn D.

Hum Mol Genet. 2024 Feb 28, .  et al. 0

Khosrowabadi E

10.1093/hmg/ddad203
- issue: - volume: - pages: .

, .  et al. 0

- issue: - volume: - pages: .

Beate, .  et al. 0

Aida I.; Alhashem

Nathalie; Doummar
Samira; Issa - issue: Kiely; Keren - volume: Boris; Kuechler - pages: Delphine; Horn.

, .  et al. 0

- issue: - volume: - pages: .

Valence S, .  et al. 0

Villard L

L
- issue: - volume: - pages: .

N. J., .  et al. 0

L.; Fontés

- issue: - volume: - pages: .

consisting of multiple proteins including UNC80 and UNC79. The predominant neuronal expression pattern and its function suggest an important role in neuronal function and disease. So far, .  et al. 0

biallelic NALCN and UNC80 variants have been described in a small number of individuals leading to infantile hypotonia

hypotonia
- issue: - volume: - pages: .

Lucas, .  et al. 0

Frédéric G.; N'guetta


- issue: - volume: - pages: .

Abidi A, .  et al. 0

Cacciagli P

- issue: - volume: - pages: .

D., .  et al. 0

W. T.; Chiurazzi

E. C.; Kooy
1997;American Journal of Medical Genetics;;0148-7299;;;;02/04/1999;07/03/2016 15:23;07/03/2016 15:23;;221-236;;4;83;;Am. J. Med. Genet.;;;;;;;;eng;;;;;PubMed;;PMID: 10208154 - issue: L.; Willems - volume: P. J.";Eighth International workshop on the fragile X syndrome and X-linked mental retardation - pages: C.; Tranebjaerg.