Patricia Delbeke

Brugge, VLG, Belgium

Last Updated: 09/26/2026

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Found 10 publications

Defining a therapeutic range for adalimumab serum concentrations in the management of pediatric noninfectious uveitis, a step towards personalized treatment.

Defining a therapeutic range for adalimumab serum concentrations in the management of pediatric noninfectious uveitis, a step towards personalized treatment.

Journal: Pediatric rheumatology online journal

Published: June 26, 2023

Paediatric cataract surgery with 27G vitrectomy instrumentation: the Ghent University Hospital Experience.

Paediatric cataract surgery with 27G vitrectomy instrumentation: the Ghent University Hospital Experience.

Journal: Frontiers in medicine

Published: March 31, 2023

Identification of Codon 146 KRAS Variants in Isolated Epidermal Nevus and Multiple Lesions in Oculoectodermal Syndrome: Confirmation of the Phenotypic Continuum of Mosaic RASopathies.

Identification of Codon 146 KRAS Variants in Isolated Epidermal Nevus and Multiple Lesions in Oculoectodermal Syndrome: Confirmation of the Phenotypic Continuum of Mosaic RASopathies.

Journal: International journal of molecular sciences

Published: March 15, 2022

DETAILED CLINICAL PHENOTYPING OF OXALATE MACULOPATHY IN PRIMARY HYPEROXALURIA TYPE 1 AND REVIEW OF THE LITERATURE.

DETAILED CLINICAL PHENOTYPING OF OXALATE MACULOPATHY IN PRIMARY HYPEROXALURIA TYPE 1 AND REVIEW OF THE LITERATURE.

Journal: Retina (Philadelphia, Pa.)

Published: May 03, 2016

Accommodation insufficiency as the first sign of Guillain-Barré syndrome.

Accommodation insufficiency as the first sign of Guillain-Barré syndrome.

Journal: Acta neurologica Belgica

Published: April 30, 2015

Severe congenital neutropenia with neurological impairment due to a homozygous VPS45 p.E238K mutation: A case report suggesting a genotype-phenotype correlation.

Severe congenital neutropenia with neurological impairment due to a homozygous VPS45 p.E238K mutation: A case report suggesting a genotype-phenotype correlation.

Journal: American journal of medical genetics. Part A

Published: March 13, 2015

Novel FRMD7 Mutations and Genomic Rearrangement Expand the Molecular Pathogenesis of X-Linked Idiopathic Infantile Nystagmus.

Novel FRMD7 Mutations and Genomic Rearrangement Expand the Molecular Pathogenesis of X-Linked Idiopathic Infantile Nystagmus.

Journal: Investigative ophthalmology & visual science

Published: February 14, 2015

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

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

Journal: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society

Published: March 14, 2014

Triad of torticollis, photophobia and epiphora in a child with a posterior fossa tumor.

Triad of torticollis, photophobia and epiphora in a child with a posterior fossa tumor.

Journal: GMS ophthalmology cases

Published: January 01, 2014

Lens subluxation with stretched ciliary processes in a girl with Goltz syndrome.

Lens subluxation with stretched ciliary processes in a girl with Goltz syndrome.

Journal: Bulletin de la Societe belge d'ophtalmologie

Published: January 01, 2013

Showing 1-10 of 10

Last Updated: 09/26/2026