Cieuta‐Walti, Cécile
40  results:
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1

Pathogenic variants in KCNQ2 cause intellectual deficiency ..:

Mary, Laura ; Nourisson, Elsa ; Feger, Claire...
American Journal of Medical Genetics Part A.  185 (2021)  6 - p. 1803-1815 , 2021
 
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2

Psychomotor development in infants and young children with ..:

Sacco, Silvia ; Bouis, Charles ; Gallard, Jennifer...
American Journal of Medical Genetics Part A.  188 (2021)  3 - p. 818-827 , 2021
 
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3

Growth curves for French people with Down syndrome from bir..:

Mircher, Clotilde ; Briceño, Laura G. ; Toulas, Jeanne...
American Journal of Medical Genetics Part A.  176 (2018)  12 - p. 2685-2694 , 2018
 
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4

Anthropometric charts and congenital anomalies in newborns ..:

Mircher, Clotilde ; Toulas, Jeanne ; Cieuta‐Walti, Cécile...
American Journal of Medical Genetics Part A.  173 (2017)  8 - p. 2166-2175 , 2017
 
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5

A novel locus for idiopathic generalized epilepsy in French..:

Kinirons, Peter ; Verlaan, Dominique J. ; Dubé, Marie‐Pierre...
American Journal of Medical Genetics Part A.  146A (2008)  5 - p. 578-584 , 2008
 
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7

Opportunities, barriers, and recommendations in Down syndro..:

Hendrix, James A. ; Amon, Angelika ; Abbeduto, Leonard...
Translational Science of Rare Diseases.  5 (2021)  3-4 - p. 99-129 , 2021
 
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8

Molecular Rescue of Dyrk1A Overexpression Alterations in Mi..:

Gu, Yuchen ; Moroy, Gautier ; Paul, Jean-Louis...
International Journal of Molecular Sciences.  21 (2020)  4 - p. 1404 , 2020
 
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12

Acute regression in young people with Down Syndrome:

Cieuta-Walti, Cécile ; Mircher, Clotilde ; Rebillat, Anne-Sophie...
European Journal of Paediatric Neurology.  21 (2017)  - p. e23 , 2017
 
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14

Safety and preliminary efficacy on cognitive performance an..:

Cieuta-Walti, Cécile ; Cuenca-Royo, Aida ; Langohr, Klaus...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.gim.2022.06.011.  , 2022
 
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