MMG PUBLICATIONS

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Results: 4196  publications found.

Ori, .  et al. 0

Alessandra; Villard

Mercedes; Armstrong
Bela; Vignoli - issue: Alexsandra; Pini - volume: Giorgio; Bisgaard - pages: Milena; Craiu.


Virginie, .  et al. 0

Laurent; Peyronnet-Roux

4-difluorobenzamide (ICA73). Immunostaining and mutant mice highlight an important role of Kv7.2-con
- issue: - volume: - pages: .


but only a tendency towards reduction. Finally, .  et al. 0

we did not found any apoptotic neurons in the pons indicating that LC neurons are not dying but are more likely loosing their catecholaminergic phenotype. In conclusion

- issue: - volume: - pages: .


Behav Genet. 2010 Jan, .  et al. 0

Roux JC

10.1007/s10519-009-9303-y
- issue: - volume: - pages: .


Whalen S, .  et al. 0

Fredriksen T

Dubourg C
- issue: Villard L - volume: Goossens M - pages: Philip N.


Raynaud M, .  et al. 0

Bonnefond JP

Chelly J
- issue: - volume: - pages: .


severity of epilepsy, .  et al. 0

and type of seizures were collected. Statistical analysis was done using the IBM SPSS Version 21 software

associated with a milder Rett phenotype
- issue: - volume: - pages: .


, .  et al. 0

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, .  et al. 0

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J Med Genet. 2010 Mar, .  et al. 0

Thienpont B

10.1136/jmg.2009.070573
- issue: - volume: - pages: .


Myers SJ, .  et al. 0

Hongjie Y

Allen J
Hehr U - issue: de Wit MCY - volume: Wilke M - pages: Villard L.


, .  et al. 0

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respectively), .  et al. 0

but not for epilepsy occurrence. SIGNIFICANCE: Various mutations in the MECP2 gene have a different influence on epilepsy

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Frédéric, .  et al. 0

Marie-Thérèse; Barcia

Serge; de Saint-Martin
SCN8A and numerous other genes have been reported - issue: mutations in STXBP1 - volume: KCNQ2 - pages: an expanding field in child neurology.


while three were missense. Three additional patients with BPNH-EDS and a mutation in FLNA are described. No phenotype-genotype correlations could be established, .  et al. 0

but these clinical data sustain the importance of cardiovascular monitoring in FLNA-BPNH patients.;2009-12;04/08/2025 08:04;04/08/2025 08:04;;1394-1398;;12;80;;J Neurol Neurosurg Psychiatry;;;;;;;;eng;;;;;;;Place: England PMID: 19917821

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J Med Genet. 2010 Feb, .  et al. 0

Mignon-Ravix C

10.1136/jmg.2009.069112
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, .  et al. 0

- issue: - volume: - pages: .


Alcaraz G, .  et al. 0

Michon FX

Mignot C
Lesca G - issue: Trauffler A - volume: Badens C - pages: De La Vaissière S.


Julitta, .  et al. 0

Nathalie; Cacciagli

which could evolve to long-lasting attacks without loss of consciousness
- issue: - volume: - pages: no.


regulation of the complement way, .  et al. 0

and co-receptor in transduction signal. Children suffering from this condition exhibit developmental delay with early-onset epilepsy

but abnormalities in electroencephalographic studies were eventually present in all cases. Different type
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