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Alice E Davidson

Showing results (11-20 of 66) with videos related to

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Acta Ophthalmologica|February 17, 2022
Posterior corneal vesicles are not associated with the genetic variants that cause posterior polymorphous corneal dystrophyPetra Liskova, Nathaniel J Hafford-Tear, Pavlina Skalicka, et al.
Genes|May 5, 2021
Non-Penetrance for Ocular Phenotype in Two Individuals Carrying Heterozygous Loss-of-Function <i>ZEB1</i> AllelesLubica Dudakova, Viktor Stranecky, Lenka Piherova, et al.
Genes|December 24, 2021
Should Patients with Kearns-Sayre Syndrome and Corneal Endothelial Failure Be Genotyped for a <i>TCF4</i> Trinucleotide Repeat, Commonly Associated with Fuchs Endothelial Corneal Dystrophy?Lubica Dudakova, Pavlina Skalicka, Alice E Davidson, et al.
Cornea|May 27, 2016
Spectrum of Clinical Signs and Genetic Characterization of Gelatinous Drop-Like Corneal Dystrophy in a Colombian FamilySara Morantes, Cerys J Evans, Ana V Valencia, et al.
Investigative Ophthalmology & Visual Science|July 20, 2019
IPSC-Derived Corneal Endothelial-like Cells Act as an Appropriate Model System to Assess the Impact of SLC4A11 Variants on Pre-mRNA SplicingKristyna Brejchova, Lubica Dudakova, Pavlina Skalicka, et al.
European Journal of Human Genetics : EJHG|June 16, 2019
CUGC for posterior polymorphous corneal dystrophy (PPCD)Alice E Davidson, Nathaniel J Hafford-Tear, Lubica Dudakova, et al.
Investigative Ophthalmology & Visual Science|October 14, 2016
Genotype-Phenotype Correlation for TGFBI Corneal Dystrophies Identifies p.(G623D) as a Novel Cause of Epithelial Basement Membrane DystrophyCerys J Evans, Alice E Davidson, Nicole Carnt, et al.
European Journal of Human Genetics : EJHG|January 12, 2012
Clinical utility gene card for: BEST1-related dystrophies (Bestrophinopathies)Simon C Ramsden, Alice E Davidson, Bart P Leroy, et al.
Molecular Vision|September 17, 2011
Autosomal dominant Best disease with an unusual electrooculographic light rise and risk of angle-closure glaucoma: a clinical and molecular genetic studySancy Low, Alice E Davidson, Graham E Holder, et al.
Annals of Human Genetics|December 3, 2014
Identification of six novel mutations in ZEB1 and description of the associated phenotypes in patients with posterior polymorphous corneal dystrophy 3Cerys J Evans, Petra Liskova, Lubica Dudakova, et al.
Pageof 7

Showing results (11-20 of 66) with videos related to

Sort By:
Pageof 7
Acta Ophthalmologica|February 17, 2022
Posterior corneal vesicles are not associated with the genetic variants that cause posterior polymorphous corneal dystrophyPetra Liskova, Nathaniel J Hafford-Tear, Pavlina Skalicka, et al.
Genes|May 5, 2021
Non-Penetrance for Ocular Phenotype in Two Individuals Carrying Heterozygous Loss-of-Function <i>ZEB1</i> AllelesLubica Dudakova, Viktor Stranecky, Lenka Piherova, et al.
Genes|December 24, 2021
Should Patients with Kearns-Sayre Syndrome and Corneal Endothelial Failure Be Genotyped for a <i>TCF4</i> Trinucleotide Repeat, Commonly Associated with Fuchs Endothelial Corneal Dystrophy?Lubica Dudakova, Pavlina Skalicka, Alice E Davidson, et al.
Cornea|May 27, 2016
Spectrum of Clinical Signs and Genetic Characterization of Gelatinous Drop-Like Corneal Dystrophy in a Colombian FamilySara Morantes, Cerys J Evans, Ana V Valencia, et al.
Investigative Ophthalmology & Visual Science|July 20, 2019
IPSC-Derived Corneal Endothelial-like Cells Act as an Appropriate Model System to Assess the Impact of SLC4A11 Variants on Pre-mRNA SplicingKristyna Brejchova, Lubica Dudakova, Pavlina Skalicka, et al.
European Journal of Human Genetics : EJHG|June 16, 2019
CUGC for posterior polymorphous corneal dystrophy (PPCD)Alice E Davidson, Nathaniel J Hafford-Tear, Lubica Dudakova, et al.
Investigative Ophthalmology & Visual Science|October 14, 2016
Genotype-Phenotype Correlation for TGFBI Corneal Dystrophies Identifies p.(G623D) as a Novel Cause of Epithelial Basement Membrane DystrophyCerys J Evans, Alice E Davidson, Nicole Carnt, et al.
European Journal of Human Genetics : EJHG|January 12, 2012
Clinical utility gene card for: BEST1-related dystrophies (Bestrophinopathies)Simon C Ramsden, Alice E Davidson, Bart P Leroy, et al.
Molecular Vision|September 17, 2011
Autosomal dominant Best disease with an unusual electrooculographic light rise and risk of angle-closure glaucoma: a clinical and molecular genetic studySancy Low, Alice E Davidson, Graham E Holder, et al.
Annals of Human Genetics|December 3, 2014
Identification of six novel mutations in ZEB1 and description of the associated phenotypes in patients with posterior polymorphous corneal dystrophy 3Cerys J Evans, Petra Liskova, Lubica Dudakova, et al.
Pageof 7