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The Journal of Craniofacial Surgery|December 29, 2010
Classification and pathogenic models of unintentional postural cranial deformities in infants: plagiocephalies and brachycephaliesGuillaume Captier, David Dessauge, Marie-Christine Picot, et al.
BMC Pediatrics|November 11, 2018
Isolated neonatal bilateral vocal cord paralysis revealing a unilateral medullary defect: a case reportCamille Brotelande, Nicolas Leboucq, Mohamed Akkari, et al.
Movement Disorders Clinical Practice|February 5, 2019
Cerebral Iron Accumulation Is Not a Major Feature of FA2H/SPG35Cecilia Marelli, Mustafa A Salih, Karine Nguyen, et al.
Developmental Medicine and Child Neurology|June 29, 2022
Cerebral sinovenous thrombosis associated with head/neck infection in children: Clues for improved managementLucie Narcy, Sabine Durand, Marion Grimaud, et al.
Annales De Biologie Clinique|July 8, 2020
[Menkes disease, a diagnosis to consider in case of severe epilepsy with hyperlactacidemia: a case report]Etienne Mondesert, Agathe Roubertie, Mathilde Girard, et al.
Neuropediatrics|January 28, 2021
Paroxysmal Dyskinesias Revealing 3-Hydroxy-Isobutyryl-CoA Hydrolase (HIBCH) DeficiencyMarie-Aude Spitz, Guy Lenaers, Majida Charif, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 10, 2025
Distinguishing atypical focal areas of signal intensity from probable low-grade gliomas in the posterior fossa of children with neurofibromatosis type 1Agnès Viguier, Bastien Estublier, Anne-Isabelle Bertozzi, et al.
Annals of Clinical and Translational Neurology|August 13, 2019
Hereditary spastic paraplegia and prominent sensorial involvement: think MAG mutations!Agathe Roubertie, Majida Charif, Pierre Meyer, et al.
Mitochondrion|May 23, 2021
Optic neuropathy linked to ACAD9 pathogenic variants: A potentially riboflavin-responsive disorder?Naig Gueguen, Julie Piarroux, Emmanuelle Sarzi, et al.
Annals of Clinical and Translational Neurology|July 26, 2023
Infantile-onset parkinsonism, dyskinesia, and developmental delay: do not forget polyglutamine defects!Heidy Baide-Mairena, Arthur Coget, Nicolas Leboucq, et al.
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