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GMS Ophthalmology Cases
|
September 5, 2020
Acute bilateral serous retinal detachments with spontaneous resolution in a 6-year-old boy
Sophie Van Camp, Steffi Vande Walle, Ingele Casteels, et al.
Case Reports in Oncology
|
May 18, 2019
Clinically Relevant Response to Cisplatin-5-Fluorouracyl in Intestinal-Type Sinonasal Adenocarcinoma with Loss of Vision: A Case Report
Jonas Claus, Mark Jorissen, Vincent Vander Poorten, et al.
Orphanet Journal of Rare Diseases
|
February 22, 2014
Novel and recurrent PITX3 mutations in Belgian families with autosomal dominant congenital cataract and anterior segment dysgenesis have similar phenotypic and functional characteristics
Hannah Verdin, Elena A Sorokina, Françoise Meire, et al.
Acta Clinica Belgica
|
January 7, 2015
Cystinosis: a new perspective
Koenraad R P Veys, Martine T P Besouw, Anne-Marie Pinxten, et al.
Strabismus
|
March 16, 2022
Association between near viewing and acute acquired esotropia in children during tablet and smartphone use
Esther Van Hoolst, Liesbet Beelen, Ivo De Clerck, et al.
European Journal of Ophthalmology
|
September 28, 2011
Continuous glucose monitoring and retinopathy of prematurity
Sophie Vanhaesebrouck, Christine Vanhole, Claire Theyskens, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases
|
April 3, 2022
In search of viable SARS-CoV-2 in the tear film: a prospective clinical study in hospitalized symptomatic patients
Laura Leysen, Heleen Delbeke, Stefanie Desmet, et al.
American Journal of Medical Genetics. Part A
|
May 15, 2012
Variability in expression of a familial 2.79 Mb microdeletion in chromosome 14q22.1-22.2
Aimé Lumaka, Christine Van Hole, Ingele Casteels, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases
|
May 11, 2023
Corrigendum to "In search of viable SARS-CoV-2 in the tear film: a prospective clinical study in hospitalized symptomatic patients" [Clin Microbiol Infect 28(8) (2022 Aug) 1172-1173]
Laura Leysen, Heleen Delbeke, Stefanie Desmet, et al.
American Journal of Ophthalmology
|
March 1, 2011
High frequency of submicroscopic chromosomal deletions in patients with idiopathic congenital eye malformations
Irina Balikova, Thomy de Ravel, Carmen Ayuso, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 85) with videos related to
Sort By:
Page
of 9
GMS Ophthalmology Cases
|
September 5, 2020
Acute bilateral serous retinal detachments with spontaneous resolution in a 6-year-old boy
Sophie Van Camp, Steffi Vande Walle, Ingele Casteels, et al.
Case Reports in Oncology
|
May 18, 2019
Clinically Relevant Response to Cisplatin-5-Fluorouracyl in Intestinal-Type Sinonasal Adenocarcinoma with Loss of Vision: A Case Report
Jonas Claus, Mark Jorissen, Vincent Vander Poorten, et al.
Orphanet Journal of Rare Diseases
|
February 22, 2014
Novel and recurrent PITX3 mutations in Belgian families with autosomal dominant congenital cataract and anterior segment dysgenesis have similar phenotypic and functional characteristics
Hannah Verdin, Elena A Sorokina, Françoise Meire, et al.
Acta Clinica Belgica
|
January 7, 2015
Cystinosis: a new perspective
Koenraad R P Veys, Martine T P Besouw, Anne-Marie Pinxten, et al.
Strabismus
|
March 16, 2022
Association between near viewing and acute acquired esotropia in children during tablet and smartphone use
Esther Van Hoolst, Liesbet Beelen, Ivo De Clerck, et al.
European Journal of Ophthalmology
|
September 28, 2011
Continuous glucose monitoring and retinopathy of prematurity
Sophie Vanhaesebrouck, Christine Vanhole, Claire Theyskens, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases
|
April 3, 2022
In search of viable SARS-CoV-2 in the tear film: a prospective clinical study in hospitalized symptomatic patients
Laura Leysen, Heleen Delbeke, Stefanie Desmet, et al.
American Journal of Medical Genetics. Part A
|
May 15, 2012
Variability in expression of a familial 2.79 Mb microdeletion in chromosome 14q22.1-22.2
Aimé Lumaka, Christine Van Hole, Ingele Casteels, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases
|
May 11, 2023
Corrigendum to "In search of viable SARS-CoV-2 in the tear film: a prospective clinical study in hospitalized symptomatic patients" [Clin Microbiol Infect 28(8) (2022 Aug) 1172-1173]
Laura Leysen, Heleen Delbeke, Stefanie Desmet, et al.
American Journal of Ophthalmology
|
March 1, 2011
High frequency of submicroscopic chromosomal deletions in patients with idiopathic congenital eye malformations
Irina Balikova, Thomy de Ravel, Carmen Ayuso, et al.
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of 9