Nicolas Deconinck

The Belgian Pediatric Clinical Research Network (BPCRN) : pediatric trial facilitation during and beyond Conect4children

Levi Hoste (UGent) , An Spiessens (UGent) , Lieve Nuytinck (UGent) , Eva Degraeuwe (UGent) , Laura Persijn (UGent) , Annelies De Maré (UGent) , Daphné Christiaens (UGent) , Mark Turner (UGent) , Karel Allegaert, Nicolas Deconinck (UGent) , et al.

(2025) BELGIAN JOURNAL OF PAEDIATRICS. 27(2). p.125-130

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Journal Article
A1
open access

Assessing the swallowing function in children with spinal muscular atrophy : an easily accessible and objective multidimensional approach

Charlotte Colot, Sarah Benmechri, Elke Everaert (UGent) , Sarah Muys (UGent) , Linde Van Himme (UGent) , Valentine Tahon (UGent) , Maurine Salmon, Dorine Van Dyck, Elke De Vos (UGent) and Nicolas Deconinck (UGent)

(2024) JOURNAL OF NEUROMUSCULAR DISEASES. 11(4). p.839-853

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Journal Article
A1
open access

Congenital hydrocephalus : new Mendelian mutations and evidence for oligogenic inheritance

Valerie Jacquemin, Nassim Versbraegen, Sarah Duerinckx, Annick Massart, Julie Soblet, Camille Perazzolo, Nicolas Deconinck (UGent) , Elise Brischoux-Boucher, Anne De Leener, Nicole Revencu, et al.

(2023) HUMAN GENOMICS. 17(1).

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Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy type 1 (STR1VE-EU) : an open-label, single-arm, multicentre, phase 3 trial

E Mercuri, F Muntoni, G Baranello, R Masson, O Boespflug-Tanguy, C Bruno, S Corti, A Daron, Nicolas Deconinck (UGent) , L Servais, et al.

(2021) LANCET NEUROLOGY. 20(10). p.832-841

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Natural history of pulmonary function in collagen VI-related myopathies

A Reghan Foley, Susana Quijano-Roy, James Collins, Volker Straub, Michelle McCallum, Nicolas Deconinck (UGent) , Eugenio Mercuri, Marika Pane, Adele D'Amico, Enrico Bertini, et al.

(2013) BRAIN. 136(12). p.3625-3633

Academic Bibliography

Nicolas Deconinck

The Belgian Pediatric Clinical Research Network (BPCRN) : pediatric trial facilitation during and beyond Conect4children

Assessing the swallowing function in children with spinal muscular atrophy : an easily accessible and objective multidimensional approach

Congenital hydrocephalus : new Mendelian mutations and evidence for oligogenic inheritance

Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy type 1 (STR1VE-EU) : an open-label, single-arm, multicentre, phase 3 trial

Natural history of pulmonary function in collagen VI-related myopathies

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