Hana Abouzeid
Avenue De France 15, CP 133
1000, Paraguay
1000, Paraguay
Last Updated: 09/26/2026
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Found 22 publications
Azacitidine-induced remission enables allogeneic transplantation in TET2/BCOR-mutant relapsed extranodal natural killer/T-cell lymphoma: a case report.
Journal: Haematologica
Published: December 09, 2025
High blood pressure and glaucoma : an inextricable link
Journal: Revue medicale suisse
Published: September 12, 2024
Acute Myopic Shift after a Single Dose of Acetazolamide: A Case Report and Review of the Literature.
Acute Myopic Shift after a Single Dose of Acetazolamide: A Case Report and Review of the Literature.
Journal: Klinische Monatsblatter fur Augenheilkunde
Published: April 23, 2024
PRESERFLO MicroShunt in Severe Myopia: A Case Report and Review of the Literature.
Journal: Klinische Monatsblatter fur Augenheilkunde
Published: April 23, 2024
Genome-wide Association Studies of Retinal Vessel Tortuosity Identify Numerous Novel Loci Revealing Genes and Pathways Associated With Ocular and Cardiometabolic Diseases.
Journal: Ophthalmology science
Published: May 25, 2022
Intraocular Pressure Reduction after Femtolaser Assisted Cataract Surgery and Its Association with the Use of Ultrasound.
Journal: Medicina (Kaunas, Lithuania)
Published: March 09, 2021
Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies.
Journal: American journal of human genetics
Published: December 17, 2016
A Novel Recessive RPGRIP1 Mutation Causing Leber Congenital Amaurosis.
Journal: Klinische Monatsblatter fur Augenheilkunde
Published: April 27, 2016
Novel ADAM9 homozygous mutation in a consanguineous Egyptian family with severe cone-rod dystrophy and cataract.
Journal: The British journal of ophthalmology
Published: August 06, 2014
Association between rate of binocular visual field change and vision-related quality of life: novel finding or spurious association?
Journal: JAMA ophthalmology
Published: June 13, 2014
Cone-rod dystrophy caused by a novel homozygous RPE65 mutation in Leber congenital amaurosis.
Journal: Klinische Monatsblatter fur Augenheilkunde
Published: April 29, 2014
Last Updated: 09/26/2026