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Benjamin Dudoignon

Showing results (41-50 of 56) with videos related to

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Chronic Respiratory Disease|December 29, 2020
Awakening efficacy of a vibrotactile device in patients on home nocturnal ventilatory assistance and healthy subjects as family caregiver proxiesValerie Attali, Sophie Lavault, Antoine Guerder, et al.
American Journal of Medical Genetics. Part A|October 27, 2019
Expanding the phenotype in Adams-Oliver syndrome correlating with the genotypeBenjamin Dudoignon, Celine Huber, Caroline Michot, et al.
European Journal of Pediatrics|January 30, 2025
European central hypoventilation syndrome consortium description of congenital central hypoventilation syndrome neonatal onsetBenjamin Dudoignon, Jochen Peters, Maria Giovanna Paglietti, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 11, 2024
A new nonsense pathogenic variant in exon 1 of PHOX2B leads to the diagnosis of congenital central hypoventilation syndrome with intra-familial variabilityMorgane Pelleter, Charlène Desaintjean, Romane Gyapay, et al.
Sleep Medicine|February 20, 2026
Residual sleep disordered breathing under ventilatory support in children: a polysomnography studyLaurianne Coutier, Sébastien Baillieul, Aurore Guyon, et al.
The European Respiratory Journal|January 28, 2022
Addition of bacterial filter alters positive airway pressure and non-invasive ventilation performancesClaudio Rabec, Emeline Fresnel, Yann Rétory, et al.
Journal of Pediatric Hematology/Oncology|February 17, 2025
PHOX2B -associated Congenital Central Hypoventilation Syndrome Revealed Upon Treatment With Dinutuximab-betaAlix Chupin, Benjamin Dudoignon, Nathalie Couque, et al.
Archives of Disease in Childhood|July 12, 2024
Non-invasive respiratory support in children and young adults with complex medical conditions in pediatric palliative careBrigitte Fauroux, Jessica Taytard, Iulia Ioan, et al.
Clinical Genetics|January 30, 2024
Further description of two individuals with de novo p.(Glu127Lys) missense variant in the ASCL1 geneMarlène Malbos, Emma Wakeling, Thierry Gautier, et al.
Sleep Medicine|April 26, 2026
The hidden burden of narcolepsy type 1: Discordance in psychobehavioral symptoms between patient self-reports and reports from close family members and friendsStéphanie Mazza, Emmanuel Fort, Nora Martel, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Chronic Respiratory Disease|December 29, 2020
Awakening efficacy of a vibrotactile device in patients on home nocturnal ventilatory assistance and healthy subjects as family caregiver proxiesValerie Attali, Sophie Lavault, Antoine Guerder, et al.
American Journal of Medical Genetics. Part A|October 27, 2019
Expanding the phenotype in Adams-Oliver syndrome correlating with the genotypeBenjamin Dudoignon, Celine Huber, Caroline Michot, et al.
European Journal of Pediatrics|January 30, 2025
European central hypoventilation syndrome consortium description of congenital central hypoventilation syndrome neonatal onsetBenjamin Dudoignon, Jochen Peters, Maria Giovanna Paglietti, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 11, 2024
A new nonsense pathogenic variant in exon 1 of PHOX2B leads to the diagnosis of congenital central hypoventilation syndrome with intra-familial variabilityMorgane Pelleter, Charlène Desaintjean, Romane Gyapay, et al.
Sleep Medicine|February 20, 2026
Residual sleep disordered breathing under ventilatory support in children: a polysomnography studyLaurianne Coutier, Sébastien Baillieul, Aurore Guyon, et al.
The European Respiratory Journal|January 28, 2022
Addition of bacterial filter alters positive airway pressure and non-invasive ventilation performancesClaudio Rabec, Emeline Fresnel, Yann Rétory, et al.
Journal of Pediatric Hematology/Oncology|February 17, 2025
PHOX2B -associated Congenital Central Hypoventilation Syndrome Revealed Upon Treatment With Dinutuximab-betaAlix Chupin, Benjamin Dudoignon, Nathalie Couque, et al.
Archives of Disease in Childhood|July 12, 2024
Non-invasive respiratory support in children and young adults with complex medical conditions in pediatric palliative careBrigitte Fauroux, Jessica Taytard, Iulia Ioan, et al.
Clinical Genetics|January 30, 2024
Further description of two individuals with de novo p.(Glu127Lys) missense variant in the ASCL1 geneMarlène Malbos, Emma Wakeling, Thierry Gautier, et al.
Sleep Medicine|April 26, 2026
The hidden burden of narcolepsy type 1: Discordance in psychobehavioral symptoms between patient self-reports and reports from close family members and friendsStéphanie Mazza, Emmanuel Fort, Nora Martel, et al.
Pageof 6