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Mariya Moosajee

Showing results (41-50 of 176) with videos related to

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BMJ Case Reports|June 22, 2021
Bilateral macular drusen in acquired partial lipodystrophy with type 2 membranoproliferative glomerulonephritisAlexander Tanner, Hwei Wuen Chan, Anna Stears, et al.
European Journal of Human Genetics : EJHG|July 31, 2019
Anophthalmia including next-generation sequencing-based approachesPhilippa Harding, Brian P Brooks, David FitzPatrick, et al.
Journal of the Royal Society of Medicine|November 3, 2004
A tense case--Carney's triadJohn C Bladen, Mariya Moosajee, J H Duncan Bassett
Therapeutic Advances in Ophthalmology|March 29, 2024
Practice patterns in reporting and documentation of Charles Bonnet syndrome: a retrospective review following COVID-19Dalia Abdulhussein, Lee Jones, Sri Harsha Dintakurti, et al.
Genes|January 26, 2021
Clinical Spectrum and Genetic Diagnosis of 54 Consecutive Patients Aged 0-25 with Bilateral CataractsSuzannah Bell, Samantha Malka, Ian Christopher Lloyd, et al.
The British Journal of Ophthalmology|May 4, 2021
Publication objectives and processes at the <i>British Journal of Ophthalmology</i>: what authors and readers need to knowFrank Larkin, Ludwig M Heindl, Mingguang He, et al.
Genes|February 10, 2021
Ocular Phenotype Associated with <i>DYRK1A</i> VariantsCécile Méjécase, Christopher M Way, Nicholas Owen, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|December 17, 2009
Transient internal ophthalmoplegia after inferior oblique myectomyJohn C Bladen, Mariya Moosajee, Romesh Angunawela, et al.
Genes|April 3, 2021
The Genetic and Clinical Features of <i>FOXL2</i>-Related Blepharophimosis, Ptosis and Epicanthus Inversus SyndromeCécile Méjécase, Chandni Nigam, Mariya Moosajee, et al.
Genes|December 22, 2019
The Spectrum of <i>PAX6</i> Mutations and Genotype-Phenotype Correlations in the EyeDulce Lima Cunha, Gavin Arno, Marta Corton, et al.
Pageof 18

Showing results (41-50 of 176) with videos related to

Sort By:
Pageof 18
BMJ Case Reports|June 22, 2021
Bilateral macular drusen in acquired partial lipodystrophy with type 2 membranoproliferative glomerulonephritisAlexander Tanner, Hwei Wuen Chan, Anna Stears, et al.
European Journal of Human Genetics : EJHG|July 31, 2019
Anophthalmia including next-generation sequencing-based approachesPhilippa Harding, Brian P Brooks, David FitzPatrick, et al.
Journal of the Royal Society of Medicine|November 3, 2004
A tense case--Carney's triadJohn C Bladen, Mariya Moosajee, J H Duncan Bassett
Therapeutic Advances in Ophthalmology|March 29, 2024
Practice patterns in reporting and documentation of Charles Bonnet syndrome: a retrospective review following COVID-19Dalia Abdulhussein, Lee Jones, Sri Harsha Dintakurti, et al.
Genes|January 26, 2021
Clinical Spectrum and Genetic Diagnosis of 54 Consecutive Patients Aged 0-25 with Bilateral CataractsSuzannah Bell, Samantha Malka, Ian Christopher Lloyd, et al.
The British Journal of Ophthalmology|May 4, 2021
Publication objectives and processes at the <i>British Journal of Ophthalmology</i>: what authors and readers need to knowFrank Larkin, Ludwig M Heindl, Mingguang He, et al.
Genes|February 10, 2021
Ocular Phenotype Associated with <i>DYRK1A</i> VariantsCécile Méjécase, Christopher M Way, Nicholas Owen, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|December 17, 2009
Transient internal ophthalmoplegia after inferior oblique myectomyJohn C Bladen, Mariya Moosajee, Romesh Angunawela, et al.
Genes|April 3, 2021
The Genetic and Clinical Features of <i>FOXL2</i>-Related Blepharophimosis, Ptosis and Epicanthus Inversus SyndromeCécile Méjécase, Chandni Nigam, Mariya Moosajee, et al.
Genes|December 22, 2019
The Spectrum of <i>PAX6</i> Mutations and Genotype-Phenotype Correlations in the EyeDulce Lima Cunha, Gavin Arno, Marta Corton, et al.
Pageof 18