Ghent University Academic Bibliography

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Genetic landscape of a cohort of children with Varicella zoster virus encephalitis, cerebellitis, and stroke

Franziska Winzig, Kerstin De Keukeleere, Esther Bartholomeus, Nicolas Deconinck, Christophe Barrea, Inge Matthijs, Anna C Jansen, Helene Verhelst (UGent) , Charlotte Dielman, Maria Kuznetsova, et al.

(2026) JOURNAL OF INFECTIOUS DISEASES. 233(3). p.510-520
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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
Cognition and communication in patients with spinal muscular atrophy : a systematic review

Sanae Akodad, Delphine De Smedt (UGent) , Simon Baijot, Hilde Stevens and Nicolas Deconinck

(2024) HELIYON. 10(13).
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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 myasthenic syndromes in Belgium : genetic and clinical characterization of pediatric and adult patients

Nathalie Smeets, Alexander Gheldof, Bart Dequeker, Margaux Poleur, Sofia Maldonado Slootjes, Vinciane Van Parijs, Nicolas Deconinck, Pauline Dontaine, Alicia Alonso-Jimenez, Jan De Bleecker (UGent) , et al.

(2024) PEDIATRIC NEUROLOGY. 158. p.57-65
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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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The flood of study feasibilities and the value of a centralized approach

Eva Degraeuwe (UGent) , Laura Persijn (UGent) , Lieve Nuytinck (UGent) , Elena Levtchenko, Nicolas Deconinck, Etienne Sokal, Saskia Vande Velde (UGent) , Olivier Gilliaux, Karl Logghe, ANN RAES, et al.

(2022) European Society of Developmental Perinal and Paediatric Pharmacology (ESDPPP) Annual Conference 2022, Abstracts.
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- Conference Paper
- C3
- open access
Paediatric clinical trial needs and requirements within Belgium

Eva Degraeuwe (UGent) , Laura Persijn (UGent) , Lieve Nuytinck (UGent) , Elena Levtchenko, Nicolas Deconinck, Etienne Sokal, Saskia Vande Velde (UGent) , Olivier Gillaux, Karl Logghe, ANN RAES, et al.

(2022) European Society of Developmental Perinal and Paediatric Pharmacology (ESDPPP) Annual Conference 2022, Abstracts.
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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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- Journal Article
- A1
- open access
Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly : high incidence of epilepsy

Sarah Duerinckx, Julie Désir, Camille Perazzolo, Cindy Badoer, Valérie Jacquemin, Julie Soblet, Isabelle Maystadt, Yusuf Tunca, Bettina Blaumeiser, Berten Ceulemans, et al.

(2021) MOLECULAR GENETICS & GENOMIC MEDICINE. 9(9).

Academic Bibliography

Genetic landscape of a cohort of children with Varicella zoster virus encephalitis, cerebellitis, and stroke

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

Cognition and communication in patients with spinal muscular atrophy : a systematic review

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

Congenital myasthenic syndromes in Belgium : genetic and clinical characterization of pediatric and adult patients

Congenital hydrocephalus : new Mendelian mutations and evidence for oligogenic inheritance

The flood of study feasibilities and the value of a centralized approach

Paediatric clinical trial needs and requirements within Belgium

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

Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly : high incidence of epilepsy

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