Sebastien B. Lebon

Lausanne, VD, Switzerland

Last Updated: 09/26/2026

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Found 52 publications

Altered structural connectivity in epilepsy with myoclonic atonic seizures.

Altered structural connectivity in epilepsy with myoclonic atonic seizures.

Journal: Epilepsy research
Published: December 19, 2025

Acute disseminated encephalomyelitis mimicking brain tumor: about 2 pediatric cases: ADEM mimicking brain tumor.

Acute disseminated encephalomyelitis mimicking brain tumor: about 2 pediatric cases: ADEM mimicking brain tumor.

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
Published: March 06, 2025

The genetic and phenotypic spectrum of GABRB1-related disorders.

The genetic and phenotypic spectrum of GABRB1-related disorders.

Journal: Brain : a journal of neurology
Published: December 19, 2024

Comprehensive genetic diagnosis and therapeutic perspectives in 155 children with developmental and epileptic encephalopathy.

Comprehensive genetic diagnosis and therapeutic perspectives in 155 children with developmental and epileptic encephalopathy.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: November 18, 2024

Prenatal diagnosis of Blake's pouch cyst: from natural history to management.

Prenatal diagnosis of Blake's pouch cyst: from natural history to management.

Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: November 11, 2024

Tuberous sclerosis: a survey in the canton of Vaud, Switzerland.

Tuberous sclerosis: a survey in the canton of Vaud, Switzerland.

Journal: Frontiers in medicine
Published: October 18, 2024

Prenatal Diagnosis of Warsaw Breakage Syndrome: Fetal Compound Heterozygous Variants in the DDX11 Gene Associated With Growth Restriction, Cerebral, and Extra-Cerebral Malformations.

Prenatal Diagnosis of Warsaw Breakage Syndrome: Fetal Compound Heterozygous Variants in the DDX11 Gene Associated With Growth Restriction, Cerebral, and Extra-Cerebral Malformations.

Journal: Prenatal diagnosis
Published: July 23, 2024

Prenatal Diagnosis of Okur-Chung Syndrome: Ultrasound Findings and Implications of CSNK2A1 and KCNQ5 Variants.

Prenatal Diagnosis of Okur-Chung Syndrome: Ultrasound Findings and Implications of CSNK2A1 and KCNQ5 Variants.

Journal: Maternal-fetal medicine (Wolters Kluwer Health, Inc.)
Published: July 23, 2024

Inflammatory Type Focal Cerebral Arteriopathy of the Posterior Circulation in Children: A Comparative Cohort Study.

Inflammatory Type Focal Cerebral Arteriopathy of the Posterior Circulation in Children: A Comparative Cohort Study.

Journal: Stroke
Published: March 06, 2024

Seizures in Children with Influenza during the 2022-2023 Winter Season, a Case Series.

Seizures in Children with Influenza during the 2022-2023 Winter Season, a Case Series.

Journal: Clinics and practice
Published: November 28, 2023

How to differentiate PHACES syndrome from Blake's pouch cyst in first half of pregnancy.

How to differentiate PHACES syndrome from Blake's pouch cyst in first half of pregnancy.

Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: February 11, 2023

Prenatal Diagnosis of Gómez-López-Hernández Syndrome.

Prenatal Diagnosis of Gómez-López-Hernández Syndrome.

Journal: Fetal diagnosis and therapy
Published: January 20, 2023
Showing 1-12 of 52

Last Updated: 09/26/2026