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: 4196  publications found.

the white matter abnormalities showed a peculiar evolution from severe hypomyelination at 4 months to patchy lesions later in childhood. Taken as a whole, .  et al. 0

these observations collectively d

- issue: - volume: - pages: .

Frank, .  et al. 0

Stephan; Villard

indicative of a universal dynamical regime for gyrokinetics
- issue: - volume: - pages: .

Epilepsy Res. 2015 Mar, .  et al. 0

Poulat AL

10.1016/j.eplepsyres.2015.01.008
- issue: - volume: - pages: .

Perrin L, .  et al. 0

Piton A

Lewis-Smith D
- issue: - volume: - pages: Depienne C. "Front Cell Dev Biol. 2022 Dec 8;10:1019715. doi: 10.3389/fcell.2022.1019715. eCollection 2022." Parenti I Front C.

Moncla A, .  et al. 0

Milh M

- issue: - volume: - pages: .

, .  et al. 0

- issue: - volume: - pages: .

, .  et al. 0

- issue: - volume: - pages: .

, .  et al. 0

- issue: - volume: - pages: .

Mol Neurobiol. 2015 Aug, .  et al. 0

El Waly B

10.1007/s12035-014-8919-y
- issue: - volume: - pages: .

Christodoulou J, .  et al. 0

Clarke AJ

Renieri A
- issue: - volume: - pages: .

Clancy K, .  et al. 0

Gardiner K.;"Gene. 1998 Mar 27;210(1):17-24. doi: 10.1016/s0378-1119(98)00032-8.";Villard L;Gene;1998;23/05/1998;;;10.1016/s0378-1119(98)00032-8

- issue: - volume: - pages: .

R., .  et al. 0

D.; De Filippis

A.; Chabrol
A.";Novel FOXG1 mutations associated with the congenital variant of Rett syndrome;Journal of Medical Genetics;;1468-6244;10.1136/jmg.2009.067884;;BACKGROUND: Rett syndrome is a severe neurodevelopmental disorder representing one of the most common geneti - issue: E.; Mari - volume: F.; Ariani - pages: A.; Pineda.

Laurent", .  et al. 0

the rate-limiting enzyme in catecholamine synthesis

- issue: - volume: - pages: .

, .  et al. 0

- issue: - volume: - pages: .

Am J Hum Genet. 2014 Jul 3, .  et al. 0

Thevenon J

10.1016/j.ajhg.2014.06.006
- issue: - volume: - pages: .

, .  et al. 0

- issue: - volume: - pages: .

Vanni N, .  et al. 0

Cacciagli P

Villard L
- issue: - volume: - pages: .

Spain and Latvia. Clinical data have been compared with the two previously reported patients with mutations in FOXG1. In all cases hypotonia, .  et al. 0

irresponsiveness and irritability were present in the neonatal period. At birth

- issue: - volume: - pages: .

AM (-35%) of Mecp2-/y mice and to a lesser extent in the PG (-11%) and AM (-18%) in Mecp2+/- mice. We evaluated in vivo the chemoreflex sensitivity of Mecp2-/y mice using whole-body plethysmography to record the breathing of Mecp2-/y mice in normoxia and in response to acute hypoxia (10% O(2)). Our results show that the hypoxic ventilatory response is significantly increased in Mecp2-/y mice (+50%) demonstrating in vivo disturbances of the chemoafferent pathway. In conclusion, .  et al. 0

our results offer new insights to better understand the mechanisms leading to autonomic dysfunction in RS.;05/12/2008;07/03/2016 15:17;23/06/2020 08:44;;82-86;;1;447;;Neurosci. Lett.;;;;;;;;eng;;;;;PubMed;;PMID: 18834926

- issue: - volume: - pages: .

, .  et al. 0

- issue: - volume: - pages: .