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Cieuta‐Walti, Cécile
40
results:
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Online (40)
Mediatypes
Articles (Online) (13)
OpenAccess-fulltext (27)
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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
Link:
https://doi.org/10.1002/..
?
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
Link:
https://doi.org/10.1002/..
?
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
Link:
https://doi.org/10.1002/..
?
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
Link:
https://doi.org/10.1002/..
?
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
Link:
https://doi.org/10.1002/..
?
6
Safety and preliminary efficacy on cognitive performance an..:
Cieuta-Walti, Cécile
;
Cuenca-Royo, Aida
;
Langohr, Klaus
...
Genetics in Medicine. 24 (2022) 10 - p. 2004-2013 , 2022
Link:
https://doi.org/10.1016/..
?
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
Link:
https://doi.org/10.3233/..
?
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
Link:
https://doi.org/10.3390/..
?
9
Methylomic profiling in trisomy 21 identifies cognition- an..:
Haertle, Larissa
;
Müller, Tobias
;
Lardenoije, Roy
...
Clinical Epigenetics. 11 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/..
?
10
Biallelic Loss-of-Function Variants in AIMP1 Cause a Rare N..:
Accogli, Andrea
;
Guerrero, Kether
;
D'Agostino, Maria Daniela
...
Journal of Child Neurology. 34 (2018) 2 - p. 74-80 , 2018
Link:
https://doi.org/10.1177/..
?
11
Acute Regression in Young People with Down Syndrome:
Mircher, Clotilde
;
Cieuta-Walti, Cécile
;
Marey, Isabelle
...
Brain Sciences. 7 (2017) 6 - p. 57 , 2017
Link:
https://doi.org/10.3390/..
?
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
Link:
https://doi.org/10.1016/..
?
13
Ictal and interictal substraction ECD-SPECT in refractory c..:
Cieuta-Walti, Cécile
;
Kaminska, Anna
;
Chiron, Catherine
...
Pediatric Research. 41 (1997) - p. 289-289 , 1997
Link:
https://doi.org/10.1203/..
?
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
Link:
https://cnrs.hal.science..
?
15
Safety and preliminary efficacy on cognitive performance an..:
Cieuta-Walti, Cécile
;
Cuenca-Royo, Aida
;
Langohr, Klaus
...
https://doi.org/10.1016/j.gim.2022.06.011. , 2022
Link:
https://hdl.handle.net/1..
1-15