Nicolas P. Deconinck
Campus Du Solbosch CP 191, Avenue F.D. Roosevelt 50, CP 151
Brussels, BRU 1050, Belgium
Brussels, BRU 1050, Belgium
Last Updated: 09/26/2026
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Found 88 publications
Impairment of lip and tongue strength in symptomatic SMA1 patients: Results from a 4-center prospective study using the IOPI.
Journal: Journal of neuromuscular diseases
Published: March 14, 2026
Efficacy and safety of risdiplam in patients with type 1 spinal muscular atrophy: a 3-year open-label extension of the two-part, phase 2 FIREFISH trial.
Journal: The Lancet. Child & adolescent health
Published: January 28, 2026
Safety and Efficacy of Tamoxifen in Patients with Duchenne muscular dystrophy: open Label Extension of TAMDMD Trial.
Journal: Neuromuscular disorders : NMD
Published: October 15, 2025
Loss of function of retinol dehydrogenase 11 causes a recessive syndrome characterized by myopathy, retinal dystrophy, juvenile cataracts, and microcephaly.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 04, 2025
Proprioceptive and visual motion detection acuity contribute to children's dynamic postural control.
Proprioceptive and visual motion detection acuity contribute to children's dynamic postural control.
Journal: Scientific reports
Published: May 22, 2025
Genetic Landscape of a Cohort of Children With Varicella Zoster Virus Encephalitis, Cerebellitis, and Stroke.
Journal: The Journal of infectious diseases
Published: April 21, 2025
Diagnostic yield of clinical exome sequencing in 868 children with neurodevelopmental disorders.
Journal: European journal of medical genetics
Published: February 06, 2025
Safety and efficacy of tamoxifen in non-ambulant patients with Duchenne muscular dystrophy: a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial (TAMDMD Group B).
Journal: Neuromuscular disorders : NMD
Published: September 16, 2024
A Systematic Literature Review of the Natural History of Respiratory, Swallowing, Feeding, and Speech Functions in Spinal Muscular Atrophy (SMA).
Journal: Journal of neuromuscular diseases
Published: June 29, 2024
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function.
Journal: Nature genetics
Published: June 16, 2024
Patients' Perceptions of Nusinersen Effects According to Their Responder Status.
Journal: Journal of clinical medicine
Published: May 09, 2024
Assessing the Swallowing Function in Children with Spinal Muscular Atrophy: An Easily Accessible and Objective Multidimensional Approach.
Journal: Journal of neuromuscular diseases
Published: May 03, 2024
Last Updated: 09/26/2026