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Cécile Cieuta‐Walti

Observed names: C Cieuta, C Cieuta-Walti, C. CIEUTA, C. Cieuta, C. Cieuta-Walti, C. Cieuta‐Walti, Cecile Cieuta, Cecile Cieuta Walti, Cecile Cieuta-Walti, Cecile Cieuta‐Walti, Cieuta, Cécile, Cieuta-Walti, Cecile, Cécile Cieuta, Cécile Cieuta-Walti
Observed institutions: Hôpital Necker-Enfants Malades, Université de Sherbrooke, Inserm, Université de Montpellier, Commissariat à l'Énergie Atomique et aux Énergies Alternatives, Centre Hospitalier Universitaire de Sherbrooke, University Medical Center Utrecht, Humboldt-Universität zu Berlin, Hôpital Fleurimont, Centre Hospitalier Universitaire de Tours, Hôpital Gui de Chauliac, Centre Hospitalier de Bigorre, Fondation Jérôme-Lejeune, Hertie Institute for Clinical Brain Research, Hôpital Saint-Vincent-de-Paul, Université Paris Descartes, Université de Montréal, Charité – Universitätsmedizin Berlin, University of Tübingen
ORCID: 0000-0003-3806-4141
Observed ORCID: 0000-0003-3806-4141
OpenAlex ID: A5062392818
Opportunities, barriers, and recommendations in Down syndrome research
2021 · James A. Hendrix, Angelika Amon, et al. · Translational Science of Rare Diseases · 127
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Ictal SPECT in children with epilepsy: comparison with intracranial EEG and relation to postsurgical outcome
2002 · A. Kaminska, C. Chiron, et al. · Brain · 94
Feeding problems and gastrointestinal diseases in Down syndrome
2019 · A. Ravel, C. Mircher, et al. · Archives de Pédiatrie · 93
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study
2018 · Patrick May, Simon Girard, et al. · The Lancet Neurology · 83
Lamotrigine in infantile spasms
1994 · Pierangelo Veggiotti, Cécile Cieuta, et al. · The Lancet · 80
Use of subtraction ictal SPECT co-registered to MRI for optimizing the localization of seizure foci in children.
1999 · P Véra, A Kaminska, et al. · PubMed · 78
Acute Regression in Young People with Down Syndrome
2017 · Clotilde Mircher, Cécile Cieuta-Walti, et al. · Brain Sciences · 77
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Early Clinical and EEG Features of Infantile Spasms in Down Syndrome
1996 · M. L. Silva, C. Cieuta, et al. · Epilepsia · 58
Influence of concurrent antiepileptic medication on the pharmacokinetics of lamotrigine as add‐on therapy in epileptic children
1996 · F. VAUZELLE‐KERVROËDAN, E. REY, et al. · British Journal of Clinical Pharmacology · 52
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Humanized mouse model of Rasmussen’s encephalitis supports the immune-mediated hypothesis
2018 · Hania Kebir, Lionel Carmant, et al. · Journal of Clinical Investigation · 42
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Safety and preliminary efficacy on cognitive performance and adaptive functionality of epigallocatechin gallate (EGCG) in children with Down syndrome. A randomized phase Ib clinical trial (PERSEUS study)
2022 · Cécile Cieuta-Walti, Aida Cuenca-Royo, et al. · Genetics in Medicine · 39
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Functional imaging in the work-up of childhood epilepsy
2001 · L. Hertz-Pannier, C. Chiron, et al. · Child s Nervous System · 33
Cot death and myocarditis
1992 · Caroline Rambaud, Cécile Cieuta, et al. · Cardiology in the Young · 30
Molecular Rescue of Dyrk1A Overexpression Alterations in Mice with Fontup® Dietary Supplement: Role of Green Tea Catechins
2020 · Yuchen Gu, Gautier Moroy, et al. · International Journal of Molecular Sciences · 29
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Epileptiform Asymetries and Treatment Response in Juvenile Myoclonic Epilepsy
2010 · Karine Létourneau, Cécile Cieuta-Walti, et al. · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 26
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Single-photon emission computed tomography: ictal perfusion in childhood epilepsies
1999 · Catherine Chiron, Pierre Vera, et al. · Brain and Development · 26
Early detection and treatment of obstructive sleep apnoea in infants with Down syndrome: a prospective, non-randomised, controlled, interventional study
2024 · Brigitte Fauroux, Silvia Sacco, et al. · The Lancet Regional Health - Europe · 25
Methylomic profiling in trisomy 21 identifies cognition- and Alzheimer’s disease-related dysregulation
2019 · Larissa Haertle, Tobias Müller, et al. · Clinical Epigenetics · 22
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Growth curves for French people with Down syndrome from birth to 20 years of age
2018 · Clotilde Mircher, Laura G. Briceño, et al. · American Journal of Medical Genetics Part A · 18
Pathogenic variants in KCNQ2 cause intellectual deficiency without epilepsy: Broadening the phenotypic spectrum of a potassium channelopathy
2021 · Laura Mary, Elsa Nourisson, et al. · American Journal of Medical Genetics Part A · 16
Anthropometric charts and congenital anomalies in newborns with Down syndrome
2017 · Clotilde Mircher, Jeanne Toulas, et al. · American Journal of Medical Genetics Part A · 15
Further delineation of BCAP31-linked intellectual disability: description of 17 new families with LoF and missense variants
2021 · Sandra Whalen, Marie Shaw, et al. · European Journal of Human Genetics · 14
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Biallelic Loss-of-Function Variants in AIMP1 Cause a Rare Neurodegenerative Disease
2018 · Andrea Accogli, Kether Guerrero, et al. · Journal of Child Neurology · 14
Efficacy and safety of methylphenidate on attention deficit hyperactivity disorder in children with Down syndrome
2021 · M. Roche, C. Mircher, et al. · Journal of Intellectual Disability Research · 13
Thyroid hormone and folinic acid in young children with Down syndrome: the phase 3 ACTHYF trial
2019 · Clotilde Mircher, Silvia Sacco, et al. · Genetics in Medicine · 13
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Works count: 64
Citation count: 1,274
H-index: 19
I10-index: 27
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