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Results: 4167  publications found.

c.1265G>A (p.R422H), .  et al. 0

c.1264C>T (p.R422C)

it emerges that the TUBA1A related lissencephaly spectrum ranges from perisylvian pachygyria
- issue: mental retardation and diplegia/tetraplegia. CONCLUSIONS: Our data highlight the presence of consistent a - volume: - pages: these features appear to be specific to TUBA1A related lissencephaly. In addition.

and the Agaricomycetes, .  et al. 0

that may be facultative plant symbionts

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Epilepsia. 2016 May, .  et al. 0

Devaux J

10.1111/epi.13366
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J Physiol. 2022 May, .  et al. 0

Biba-Maazou N

10.1113/JP282536
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Fontés M, .  et al. 0

Saugier-Veber P

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Adeline, .  et al. 0

Laurent; Roux

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, .  et al. 0

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, .  et al. 0

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J Genet. 2016 Mar, .  et al. 0

Lacoste C

10.1007/s12041-016-0619-0
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Epilepsia. 2023 Jun, .  et al. 0

Mignon-Ravix C

10.1111/epi.17603
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Le Fur Y, .  et al. 0

Villard L

- issue: - volume: - pages: .

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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