Research Explorer

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Researcher

Franny Faes

8 Results

2021

Children with (probable) DCD at the age of three years : a case-control study

Amy De RoubaixHilde Van WaelveldeFranny FaesGrietje DewitteNina Vens

Diagnosing autism spectrum disorder in toddlers born very preterm : estimated prevalence and usefulness of screeners and the Autism Diagnostic Observation Schedule (ADOS)

Julie VermeirschLiedewij VerhaegheAlexandra CasaerFranny FaesAnna OostraHerbert Roeyers

A1 Journal Article in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS

Enhanced cGAS-STING-dependent interferon signaling associated with mutations in ATAD3A

Alice LepelleyErika Della MinaErika Van NieuwenhoveLise WaumansSylvie FraitagGillian I. RiceAshish DhirMarie-Louise FremondMathieu P. RoderoLuis Seabra et al.

A1 Journal Article in JOURNAL OF EXPERIMENTAL MEDICINE

2019

Hypotonia and delayed motor development as an early presentation of Lowe syndrome : case report and literature review

Sara DavidKATHLEEN DE WAELEBram De WildeFranny FaesOlivier VanakkerSOPHIE WALRAEDTAgnieszka Prytula-Ebels

A1 Journal Article in ACTA CLINICA BELGICA

2015

Genomic aberrations of the CACNA2D1 gene in three patients with epilepsy and intellectual disability

Sarah VergultAnnelies DheedeneAlfred MeursFranny FaesBertrand IsidorSandra JanssensAgnès GautierCédric Le CaignecBjörn Menten

A1 Journal Article in EUROPEAN JOURNAL OF HUMAN GENETICS

2014

Congenital fixed dilated pupils due to ACTA2-multisystemic smooth muscle dysfunction syndrome

Françoise MJ RoulezFranny FaesPatricia DelbekePatrick Van BogaertGeorges RodeschJulie De ZaeytijdFanny DepassePaul CouckeFrancoise M Meire

A1 Journal Article in JOURNAL OF NEURO-OPHTHALMOLOGY

1998

Urinary hydrocolpos, cloacal malformation and pre-axial polydactyly: A rare variant of neonatal hydrocolpos.

K SMETSFranny FaesPiet Hoebeke

A1 Journal Article in AMERICAN JOURNAL OF PERINATOLOGY

1997

Autopsy diagnosis of the Smith-Lemli-Opitz syndrome

Franny FaesELI VercruysseGeorges DacremontAnne De PaepeJuliaan Leroy