Academic Bibliography

Search 200 years of publications by Ghent University researchers.

Franny Faes

Ghent University Hospital

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- Conference Paper
- C3
Longitudinal development of preschoolers with probable DCD

Amy De Roubaix (UGent) , Herbert Roeyers (UGent) , Dominique Van de Velde (UGent) , Lynn Bar-On (UGent) , Grietje Dewitte (UGent) and Franny Faes (UGent)

(2023) DCD-UK 2023 Conference, Abstracts.
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- Conference Paper
- C3
- open access
Children with (probable) DCD at the age of three years : a case-control study

Amy De Roubaix (UGent) , Hilde Van Waelvelde (UGent) , Franny Faes (UGent) , Grietje Dewitte (UGent) and Nina Vens (UGent)

(2021) The UK’s 8th Biennial Academic and Practitioner Conference on Developmental Coordination Disorder, Abstracts.
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- Journal Article
- A1
- open access
Enhanced cGAS-STING-dependent interferon signaling associated with mutations in ATAD3A

Alice Lepelley, Erika Della Mina, Erika Van Nieuwenhove, Lise Waumans, Sylvie Fraitag, Gillian I. Rice, Ashish Dhir, Marie-Louise Fremond, Mathieu P. Rodero, Luis Seabra, et al.

(2021) JOURNAL OF EXPERIMENTAL MEDICINE. 218(10).
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- A1
- open access
Diagnosing autism spectrum disorder in toddlers born very preterm : estimated prevalence and usefulness of screeners and the Autism Diagnostic Observation Schedule (ADOS)

Julie Vermeirsch, Liedewij Verhaeghe (UGent) , Alexandra Casaer, Franny Faes (UGent) , Anna Oostra (UGent) and Herbert Roeyers (UGent)

(2021) JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS. 51(5). p.1508-1527
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Hypotonia and delayed motor development as an early presentation of Lowe syndrome : case report and literature review

Sara David, Kathleen De Waele (UGent) , Bram De Wilde (UGent) , Franny Faes (UGent) , Olivier Vanakker (UGent) , SOPHIE WALRAEDT (UGent) and Agnieszka Prytula-Ebels (UGent)

(2019) ACTA CLINICA BELGICA. 74(6). p.460-464
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Genomic aberrations of the CACNA2D1 gene in three patients with epilepsy and intellectual disability

Sarah Vergult (UGent) , Annelies Dheedene (UGent) , Alfred Meurs (UGent) , Franny Faes (UGent) , Bertrand Isidor, Sandra Janssens (UGent) , Agnès Gautier, Cédric Le Caignec and Björn Menten (UGent)

(2015) EUROPEAN JOURNAL OF HUMAN GENETICS. 23(5). p.628-632
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Congenital fixed dilated pupils due to ACTA2-multisystemic smooth muscle dysfunction syndrome

Françoise MJ Roulez, Franny Faes (UGent) , Patricia Delbeke, Patrick Van Bogaert, Georges Rodesch, Julie De Zaeytijd (UGent) , Fanny Depasse, Paul Coucke (UGent) and Francoise M Meire

(2014) JOURNAL OF NEURO-OPHTHALMOLOGY. 34(2). p.137-143
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- Journal Article
- A1
Urinary hydrocolpos, cloacal malformation and pre-axial polydactyly: A rare variant of neonatal hydrocolpos.

K SMETS, Franny Faes (UGent) and Piet Hoebeke (UGent)

(1998) AMERICAN JOURNAL OF PERINATOLOGY. 15(4). p.269-272
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- Conference Paper
- C3
Autopsy diagnosis of the Smith-Lemli-Opitz syndrome

Franny Faes (UGent) , ELI Vercruysse, Georges Dacremont, Anne De Paepe (UGent) and Juliaan Leroy (UGent)

(1997) AMERICAN JOURNAL OF MEDICAL GENETICS. 68(3). p.340-341