Product
Help
Pricing
About
Jobs
Log in
Get started
Author
Add to collection
Marie Laure Moutard
Observed name:
Moutard, Marie Laure
Institutions:
Hôpital Armand-Trousseau,
Assistance Publique – Hôpitaux de Paris
Observed institutions:
Inserm,
Hôpital Armand-Trousseau,
Assistance Publique – Hôpitaux de Paris,
Hôpital Saint-Vincent-de-Paul,
NeuroDiderot,
Université Pierre-et-Marie-Curie
show all 6
OpenAlex ID:
A5111626470
MRI of the fetal posterior fossa
2004
·
Catherine Adamsbaum
, Marie Laure Moutard
, et al.
·
Pediatric Radiology
·
204
Outcomes Associated With Isolated Agenesis of the Corpus Callosum: A Meta-analysis
2016
·
Francesco D’Antonio
, Giorgio Pagani
, et al.
·
PEDIATRICS
·
182
PDF
GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex
2010
·
Nadia Bahi-Buisson
, Karine Poirier
, et al.
·
Brain
·
148
PDF
LIS1-Related Isolated Lissencephaly
2009
·
Yoann Saillour
, Nathalie Carion
, et al.
·
Archives of Neurology
·
108
PDF
Spectrum of epilepsy in terminal 1p36 deletion syndrome
2007
·
Nadia Bahi‐Buisson
, Eva Guttierrez‐Delicado
, et al.
·
Epilepsia
·
66
The location of DCX mutations predicts malformation severity in X-linked lissencephaly
2008
·
Pierre-Louis Leger
, Isabelle Souville
, et al.
·
Neurogenetics
·
47
Severe Relapse of Epilepsy after Vigabatrin Withdrawal: For How Long Should We Treat Symptomatic Infantile Spasms?
2007
·
Judith Kröll‐Seger
, Anna Kaminska
, et al.
·
Epilepsia
·
35
PDF
CDK5RAP2 primary microcephaly is associated with hypothalamic, retinal and cochlear developmental defects
2020
·
Hala Nasser
, Liza Vera
, et al.
·
Journal of Medical Genetics
·
27
PDF
PAK3 mutations responsible for severe intellectual disability and callosal agenesis inhibit cell migration
2019
·
Kévin Duarte
, Solveig Heide
, et al.
·
Neurobiology of Disease
·
24
PDF
Inherited microdeletion in Xp21.3–22.1 involved in non‐specific mental retardation
1998
·
Vincent des Portes
, Alain Carrié
, et al.
·
Clinical Genetics
·
14
Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients (Genetics in Medicine, (2019), 21, 4, (837-849), 10.1038/s41436-018-0268-1)
2019
·
Mignot, Cyril
, McMahon, Aoife C.
, et al.
·
Utrecht University Repository (Utrecht University)
Whole exome sequencing in non progressive congenital ataxia consanguineous families: 3 genes lumping with early infantile epileptic encephalopathies
2017
·
Stéphanie Valence
, Catherine Garel
, et al.
·
European Journal of Paediatric Neurology
Show more works
View as search
Works count:
12
Citation count:
855
H-index:
10
I10-index:
10
Year
Topic
Type