Caroline Lacoste

Place Amélie Raba Léon
Bordeaux, 33076, France

Last Updated: 09/26/2026

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Found 26 publications

Burst-Suppression EEG in Early Infantile Developmental and Epileptic Encephalopathies: Phenotype, Genotype, and Outcome.

Burst-Suppression EEG in Early Infantile Developmental and Epileptic Encephalopathies: Phenotype, Genotype, and Outcome.

Journal: Neurology
Published: May 26, 2026

Study protocol FRENCH-ARRIVE: labor induction in low-risk nulliparous women at 39 weeks of gestation to reduce cesarean births: a randomized trial of induction versus expectant management in France.

Study protocol FRENCH-ARRIVE: labor induction in low-risk nulliparous women at 39 weeks of gestation to reduce cesarean births: a randomized trial of induction versus expectant management in France.

Journal: BMC pregnancy and childbirth
Published: February 09, 2026

Oral ivermectin versus 5% permethrin cream to treat children and adults with classic scabies: multicentre, assessor blinded, cluster randomised clinical trial.

Oral ivermectin versus 5% permethrin cream to treat children and adults with classic scabies: multicentre, assessor blinded, cluster randomised clinical trial.

Journal: BMJ (Clinical research ed.)
Published: January 06, 2026

Prostaglandins versus transcervical balloon for induction of labor for fetal growth restriction: study protocol for a randomized, multicenter, open-label, superiority trial (PROBIN).

Prostaglandins versus transcervical balloon for induction of labor for fetal growth restriction: study protocol for a randomized, multicenter, open-label, superiority trial (PROBIN).

Journal: BMC pregnancy and childbirth
Published: January 05, 2026

Molecular and clinical descriptions of patients with GABAA receptor gene variants (GABRA1, GABRB2, GABRB3, GABRG2): A cohort study, review of literature, and genotype-phenotype correlation.

Molecular and clinical descriptions of patients with GABAA receptor gene variants (GABRA1, GABRB2, GABRB3, GABRG2): A cohort study, review of literature, and genotype-phenotype correlation.

Journal: Epilepsia
Published: February 10, 2022

The EPIGENE network: A French initiative to harmonize and improve the nationwide diagnosis of monogenic epilepsies.

The EPIGENE network: A French initiative to harmonize and improve the nationwide diagnosis of monogenic epilepsies.

Journal: European journal of medical genetics
Published: May 05, 2021

Novel partial loss-of-function variants in the tyrosyl-tRNA synthetase 1 (YARS1) gene involved in multisystem disease.

Novel partial loss-of-function variants in the tyrosyl-tRNA synthetase 1 (YARS1) gene involved in multisystem disease.

Journal: European journal of medical genetics
Published: July 08, 2020

Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients.

Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 04, 2018

IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients.

IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: April 17, 2018

Clinical study of 19 patients with SCN8A-related epilepsy: Two modes of onset regarding EEG and seizures.

Clinical study of 19 patients with SCN8A-related epilepsy: Two modes of onset regarding EEG and seizures.

Journal: Epilepsia
Published: April 13, 2018

Loss-of-Function Mutations in UNC45A Cause a Syndrome Associating Cholestasis, Diarrhea, Impaired Hearing, and Bone Fragility.

Loss-of-Function Mutations in UNC45A Cause a Syndrome Associating Cholestasis, Diarrhea, Impaired Hearing, and Bone Fragility.

Journal: American journal of human genetics
Published: October 25, 2017

Missense mutation of TTC7A mimicking tricho-hepato-enteric (SD/THE) syndrome in a patient with very-early onset inflammatory bowel disease.

Missense mutation of TTC7A mimicking tricho-hepato-enteric (SD/THE) syndrome in a patient with very-early onset inflammatory bowel disease.

Journal: European journal of medical genetics
Published: March 17, 2017
Showing 1-12 of 26

Last Updated: 09/26/2026