MMG PUBLICATIONS

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Results: 4196  publications found.

the sequential appearance of the in vivo deficits in this mouse line. The observed deficits initially concern major parameters (such as body weight), .  et al. 0

and are followed by involuntary and sensitive defects (reflexes). Subsequently

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Andrew K., .  et al. 0

Véronique; Burnet

Laura B. K.; Moncla
- issue: neuropharmacology - volume: immunohistochemistry - pages: Gérard";Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice.;The Journal of neuroscience : the official journal of the Society for Neuroscience;;1529-2401 0270-6474;10.1523/JNEUROSCI.4373-05.2005;;"Rett syndrome is a severe X-linked .

and white-matter changes, .  et al. 0

which together define an X-linked syndrome. In the primary fibroblasts of affected individuals

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Rev Neurol (Paris). 2016 Mar, .  et al. 0

Milh M

10.1016/j.neurol.2016.02.005
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Desbordes de Cepoy P, .  et al. 0

Aeby A

Riquet A
Van Gils J - issue: Vermersch AI - volume: Altuzarra C - pages: Valton L.

Villard L, .  et al. 0

Roux JC.;"Behav Brain Res. 2011 Jan 1;216(1):313-20. doi: 10.1016/j.bbr.2010.08.011. Epub 2010 Aug 14.";Pratte M;Behav Brain Res;2011;18/08/2010;;;10.1016/j.bbr.2010.08.011

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Angus, .  et al. 0

Bruria; Pineda

Ana; Mari
Francesca; Ravn - issue: Anne-Marie; Mejaški Bošnjak - volume: Vlatka; Polgár - pages: Giorgio; Djuric.

even in Mecp2-/y mice that showed a normal breathing pattern. Between 1 and 2 months of age, .  et al. 0

all unanesthetized Mecp2-/y mice showed breathing disturbances that worsened until fatal respiratory arrest at approximately 2 months of age. During their last week of life

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, .  et al. 0

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Epilepsia. 2015 Dec, .  et al. 0

Di Meglio C

10.1111/epi.13214
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, .  et al. 0

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Popp B, .  et al. 0

Tamer C

Hellenbroich Y
Villard L - issue: von Spiczak S - volume: Tönnies H - pages: Rauch A.

, .  et al. 0

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, .  et al. 0

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Hum Mutat. 2015 Dec, .  et al. 0

Grozeva D

10.1002/humu.22901
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GABRG2): A cohort study, .  et al. 0

review of literature

L
Lesca G - issue: Ward - volume: Spitz MA - pages: Porter LF.

Louboutin JP, .  et al. 0

Recan D

Fontes M.;"Eur J Hum Genet. 2000 Feb;8(2):125-9. doi: 10.1038/sj.ejhg.5200432.";Villard L;Eur J Hum Genet;2000;11/04/2000;;;10.1038/sj.ejhg.5200432
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, .  et al. 0

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E., .  et al. 0

C.; McMahon

O.; Novara
and epilepsy associated with 5q14.3-q15 deletion.;Neurology;;1526-632X 0028-3878;10.1212/01.wnl.0000336339.08878.2d;;BACKGROUND: Periventricular heterotopia (PH) is an etiologically heterogeneous disorder characterized by nodules of neurons ectopically p - issue: I. E.; Guerrini - volume: R.";Periventricular heterotopia - pages: H. R.; Moncla.

, .  et al. 0

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