Publications by authors named "Sebastien Lebon"

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Acute disseminated encephalomyelitis mimicking brain tumor: about 2 pediatric cases: ADEM mimicking brain tumor.
Francesca Albertini, Mériam Koob, Stephane Darteyre, Sébastien Lebon

Arch Pediatr· October 2025

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The genetic and phenotypic spectrum of GABRB1-related disorders.
Charissa Millevert, Anthony Sze Hon Kan, Moritz Hanke, Mahmoud Koko, Maryam Erfanian Omidvar, Sébastien Lebon

Brain· June 2025

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Prenatal Diagnosis of Okur-Chung Syndrome: Ultrasound Findings and Implications of CSNK2A1 and KCNQ5 Variants.
Chiara Kratochwila, Joanna Sichitiu, Sébastien Lebon, Camille Kumps, Léo Pomar

Matern Fetal Med· April 2025

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Tuberous sclerosis: a survey in the canton of Vaud, Switzerland.
Olivia Hagon-Nicod, Florence Fellmann, Jan Novy, Sébastien Lebon, Christian Wider

Front Med (Lausanne)· December 2024

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Inflammatory Type Focal Cerebral Arteriopathy of the Posterior Circulation in Children: A Comparative Cohort Study.
Nedelina Slavova, Robin Muenger, Iciar Sanchez-Albisua, Maria Regényi, Gabriela Oesch, Sébastien Lebon

Stroke· April 2024

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Seizures in Children with Influenza during the 2022-2023 Winter Season, a Case Series.
Francesca Peranzoni, Carine Martins, Sébastien Lebon, Pierre Alex Crisinel, Marie-Helena Perez

Clin Pract· January 2024

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Prenatal Diagnosis of Gómez-López-Hernández Syndrome.
Leo Pomar, Wawrzyniec Rieder, Estelle Dubruc, Fabienne Giuliano, Isis Atallah, Sébastien Lebon

Fetal Diagn Ther· July 2023

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Developmental disorder and spastic paraparesis in two sisters with a TCF7L2 truncating variant inherited from a mosaic mother.
Beryl Royer-Bertrand, Sébastien Lebon, Ailsa Craig, Johanna Maeder, Laureane Mittaz-Crettol

Am J Med Genet A· June 2023

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Treatment-emergent adverse events and antiseizure medication actual drug load.
Tiffany Prétat, Irene Aícua-Rapún, Pascal André, Sebastien Lebon, Andrea O Rossetti

Epilepsy Behav· December 2022

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Prenatal diagnosis of Aicardi syndrome based on a suggestive imaging pattern: A multicenter case-series.
Léo Pomar, José Ochoa, Sara Cabet, Thierry A G M Huisman, Dario Paladini, Sébastien Lebon

Prenat Diagn· April 2022

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Biallelic variants in cause a severe neurodevelopmental disorder with microcephaly, bilateral cataract, epilepsy and simplified gyration.
Maria Lisa Dentici, Viola Alesi, Mathieu Quinodoz, Barbara Robens, Andrea Guerin, Sébastien Lebon

J Med Genet· March 2022

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Structural brain abnormalities in epilepsy with myoclonic atonic seizures.
Solange Denervaud, Christian Korff, Joël Fluss, Judith Kalser, Eliane Roulet-Perez, Sébastien Lebon

Epilepsy Res· November 2021

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Pediatric Encephalopathy: Clinical, Biochemical and Cellular Insights into the Role of Gln52 of and for the Dominant Disease.
Gonzalo P Solis, Tatyana V Kozhanova, Alexey Koval, Svetlana S Zhilina, Tatyana I Mescheryakova, Sébastien Lebon

Cells· October 2021

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De novo variants in CACNA1E found in patients with intellectual disability, developmental regression and social cognition deficit but no seizures.
Beryl Royer-Bertrand, Marine Jequier Gygax, Katarina Cisarova, Jill A Rosenfeld, Jennifer A Bassetti, Sebastien Lebon

Mol Autism· October 2021

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Exposure to alirocumab during the first trimester of pregnancy: A case report.
Yann Vuignier, Floriane Beaud, Christophe Kosinski, Alice Panchaud, Sébastien Lebon

Birth Defects Res· September 2021

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Agenesis of the Corpus Callosum with Facial Dysmorphism and Intellectual Disability in Sibs Associated with Compound Heterozygous Variants.
Sébastien Lebon, Mathieu Quinodoz, Virginie G Peter, Carole Gengler, Gaëlle Blanchard

Genes (Basel)· September 2021

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LBSL: Case Series and DARS2 Variant Analysis in Early Severe Forms With Unexpected Presentations.
Menno D Stellingwerff, Sonia Figuccia, Emanuele Bellacchio, Karin Alvarez, Claudia Castiglioni, Sebastien Lebon

Neurol Genet· April 2021

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Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome.
Silvia Masnada, Anna Pichiecchio, Manuela Formica, Filippo Arrigoni, Paola Borrelli, Sebastien Lebon

Neurology· March 2021

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Sultiame pharmacokinetic profile in plasma and erythrocytes after single oral doses: A pilot study in healthy volunteers.
Kim Dao, Paul Thoueille, Laurent A Decosterd, Thomas Mercier, Monia Guidi, Sébastien Lebon

Pharmacol Res Perspect· February 2020

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Childhood neurodegeneration associated with a specific UBTF variant: a new case report and review of the literature.
Filipa Bastos, Mathieu Quinodoz, Marie-Claude Addor, Beryl Royer-Bertrand, Heidi Fodstad, Sebastien Lebon

BMC Neurol· January 2020

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Clinical Reasoning: Rapidly progressive gait disorder and cranial nerves involvement in a 9-year-old boy.
Alexandra Lipp, Cécile Adam, Jean-Philippe Brouland, Mahmoud Messerer, Jean-Baptiste Armengaud, Sébastien Lebon

Neurology· January 2020

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Midazolam as a first-line treatment for neonatal seizures: Retrospective study.
Kim Dao, Eric Giannoni, Manuel Diezi, Eliane Roulet-Perez, Sebastien Lebon

Pediatr Int· May 2018

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Autosomal recessive primary microcephaly due to ASPM mutations: An update.
Pascaline Létard, Séverine Drunat, Yoann Vial, Sarah Duerinckx, Anais Ernault, Sébastien Lebon

Hum Mutat· March 2018

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Periinsular anterior quadrantotomy: technical note.
Giulia Cossu, Sebastien Lebon, Margitta Seeck, Etienne Pralong, Mahmoud Messerer

J Neurosurg Pediatr· February 2018

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[Pediatrics - New classification of seizures and epilepsies].
Sébastien Lebon, Éliane Roulet-Perez

Rev Med Suisse· January 2018

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