Ghent University Academic Bibliography

Examining differences in internet use aspects among people with intellectual disabilities in Flanders

Sarah Anrijs (UGent) , Nathalie Drooghmans, Heleen Neerinckx, Davy Nijs, Ilse Mariën, Lieven De Marez (UGent) and Koen Ponnet (UGent)

(2022) TELEMATICS AND INFORMATICS. 69.

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Postural balance problems in people with intellectual disabilities : do not forget the sensory input systems

Laura Leyssens (UGent) , Ruth Van Hecke (UGent) , Karlien Moons (UGent) , Sofie Luypaert (UGent) , Maya Danneels (UGent) , Julie Patru, Melina Willems and Leen Maes (UGent)

(2022) JOURNAL OF APPLIED RESEARCH IN INTELLECTUAL DISABILITIES. 35(1). p.280-294

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Relational ethics, informed consent, and informed assent in participatory research with children with complex communication needs

Leni Van Goidsenhoven and Elisabeth De Schauwer (UGent)

(2022) DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY.

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Vestibular function in adults with intellectual disabilities : feasibility and outcome of a vestibular screening protocol in Special Olympics athletes

Laura Leyssens (UGent) , Ruth Van Hecke (UGent) , Karlien Moons (UGent) , Sofie Luypaert (UGent) , Melina Willems, Maya Danneels (UGent) , Sarie Martens (UGent) , Cleo Dhondt (UGent) and Leen Maes (UGent)

(2021) INTERNATIONAL JOURNAL OF AUDIOLOGY. 60(6). p.446-457

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Lessons from Ricoeur’s ‘capable human being’ for practices of personalisation in three European countries

Toon Benoot (UGent) , Wouter Dursin (UGent) , Bram Verschuere (UGent) and Rudi Roose (UGent)

(2021) DISABILITY & SOCIETY. 36(5). p.772-794

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Phenotypic spectrum of the RBM10-mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome features

Candy Kumps (UGent) , Erika D'haenens (UGent) , Sarah Vergult (UGent) , Jasmine Leus, Rudy Van Coster (UGent) , Anna Jansen, Koen Devriendt, Anna Oostra (UGent) and Olivier Vanakker (UGent)

(2021) CLINICAL GENETICS. 99(3). p.449-456

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A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 gene (ZFHX3)

Maria del Rocio Pérez Baca (UGent) , Eva Jacobs, Lies Vantomme (UGent) , Mareike Bauer, Melissa Bellini, Claire Beneteau, Natasha Brown, David Coman, Laurenz De Cock (UGent) , Annelies Dheedene (UGent) , et al.

(2021) Online Research Day 2021, Abstracts.

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Two cases of DCDC2‐related neonatal sclerosing cholangitis with developmental delay and literature review

Hannes Syryn (UGent) , Anne Hoorens (UGent) , Tassos Grammatikopoulos, Maesha Deheragoda, Sofie Symoens (UGent) , Saskia Vande Velde (UGent) , Stephanie Van Biervliet (UGent) , Myriam Van Winckel (UGent) , Patrick Verloo (UGent) , Bert Callewaert (UGent) , et al.

(2021) CLINICAL GENETICS. 100(4). p.447-452

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Journal Article
A1
open access

Co‐designing the Cabriotraining : a training for transdisciplinary teams

Sofie Sergeant, Alice P. Schippers, Henriëtte Sandvoort, Sanneke Duijf, Remco Mostert, Petri J. C. M. Embregts and Geert Van Hove (UGent)

(2021) BRITISH JOURNAL OF LEARNING DISABILITIES. 49(2). p.230-246

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Journal Article
A1
open access

IQSEC2 disorder : a new disease entity or a Rett spectrum continuum?

Diego Lopergolo, Flavia Privitera, Giuseppe Castello, Caterina Lo Rizzo, Maria Antonietta Mencarelli, Anna Maria Pinto, Francesca Ariani, Aurora Currò, Vittoria Lamacchia, Roberto Canitano, et al.

(2021) CLINICAL GENETICS. 99(3). p.462-474

Academic Bibliography

Examining differences in internet use aspects among people with intellectual disabilities in Flanders

Postural balance problems in people with intellectual disabilities : do not forget the sensory input systems

Relational ethics, informed consent, and informed assent in participatory research with children with complex communication needs

Vestibular function in adults with intellectual disabilities : feasibility and outcome of a vestibular screening protocol in Special Olympics athletes

Lessons from Ricoeur’s ‘capable human being’ for practices of personalisation in three European countries

Phenotypic spectrum of the RBM10-mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome features

A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 gene (ZFHX3)

Two cases of DCDC2‐related neonatal sclerosing cholangitis with developmental delay and literature review

Co‐designing the Cabriotraining : a training for transdisciplinary teams

IQSEC2 disorder : a new disease entity or a Rett spectrum continuum?

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