Cerebral ischemia: a frequent complication of large traumatic epidural hematoma in infants

Autor: Matthieu Landart, Sandro Benichi, Lelio Guida, Marilena Lazarescu, Marie Bourgeois, Hélène Sauvé-Martin, Raphael Levy, Charles-Joris Roux, Syril James, Timothée de Saint-Denis, Estelle Vergnaud, Giovanna Paternoster, Kevin Beccaria, Thomas Blauwblomme

Publikováno v: Journal of Neurosurgery: Pediatrics. :1-5

OBJECTIVE Epidural hematoma (EDH) has rarely been studied specifically in infants. The objective of this study was to investigate the outcomes of patients aged < 18 months (infants) with EDH. METHODS The authors conducted a single-center retrospectiv

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::35ac1d5130b8250b5fe6004f41876c3c
https://doi.org/10.3171/2023.1.peds22324

Impact of sleep‐disordered breathing on the management of children with Chiari malformation type I

Autor: Foteini Vagianou, Sonia Khirani, Timothée De Saint Denis, Kevin Beccaria, Alessandro Amaddeo, Sylvain Breton, Syril James, Giovanna Paternoster, Eric Arnaud, Michel Zerah, Brigitte Fauroux

Publikováno v: Pediatric Pulmonology. 57:2954-2962

Children with Chiari malformation type I (CM-I) have an increased risk of sleep apnea. The aim of the study was to describe the management of CM-I patients in relation to symptoms, magnetic resonance imaging (MRI) findings and sleep apnea syndrome (S

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3e84e094f5bf066aac9c848821ff904
https://doi.org/10.1002/ppul.26113

The Challenge of Gene Therapy for Neurological Diseases: Strategies and Tools to Achieve Efficient Delivery to the Central Nervous System

Autor: Guillaume Wurtz, Michel Zerah, Emilie Audouard, Françoise Piguet, Arthur André, Timothée de Saint Denis, Raphael Schatz, Nathalie Cartier, Caroline Sevin, Sandro Alves, Kevin Beccaria

Publikováno v: Human Gene Therapy
Human Gene Therapy, 2021, 32 (7-8), pp.349-374. ⟨10.1089/hum.2020.105⟩
Human Gene Therapy, Mary Ann Liebert, 2021, 32 (7-8), pp.349-374. ⟨10.1089/hum.2020.105⟩

International audience; For more than ten years, gene therapy for neurological diseases has experienced intensive research growth and more recently therapeutic interventions for multiple indicationsBeneficial results in several phase 1/2 clinical stu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e135e295cc8ada193184c0465b367996
https://doi.org/10.1089/hum.2020.105

Spinal dysraphism as a new entity in V.A.C.TE.R.L syndrome, resulting in a novel acronym V.A.C.TE.R.L.S

Autor: M. Zerah, Aymeric Amelot, Timothée de Saint Denis, Martin Catala, Célia Cretolle, Sabine Sarnacki

Publikováno v: European Journal of Pediatrics. 179:1121-1129

Anorectal malformation (ARM) is the most common symptom in VACTERL syndrome (vertebral, anal, cardiac, tracheo-esophageal fistula, renal, and limb anomalies). The association of ARM and spinal dysraphisms (DYS) is well documented. We aim to better ev

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f08ec5522470a944b4b0a108711501c7
https://doi.org/10.1007/s00431-020-03609-4

The Myelic Limited Dorsal Malformation: Prenatal Ultrasonographic Characteristics of an Intermediate Form of Dysraphism

Autor: Ferdinand Dhombres, Paul Maurice, Eléonore Blondiaux, Lucie Guilbaud, Emeline Maisonneuve, Pauline Lallemant-Dudek, Jean-Marie Jouannic, Timothée de Saint-Denis, Catherine Garel, Hubert Ducou Le Pointe, Michel Zerah, Saskia Vande Perre

Publikováno v: Fetal diagnosis and therapy. 48(9)

Objectives: The aim of the study was to report a subtype of dysraphism designated as myelic limited dorsal malformation (MyeLDM) and to describe its characteristics at prenatal ultrasound (US). Methods: It was a retrospective study from 2014 to 2020

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5bc9d7ab0196c548679b0dc12d6a380
https://pubmed.ncbi.nlm.nih.gov/34814137