Patrik Schatz

Scopus Author ID ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2016-2021
Publications (10 Years): 21

Top Topics

Optical Coherence Tomography

Diabetic Retinopathy

Cataract Surgery

Top Venues

Ophthalmic genetics

Scientific reports

Neuro-ophthalmology (Aeolus Press)

Acta ophthalmologica

This page only lists publications with an associated author ORCID identifier.

Publications

Budoor Albabtain, Marco Mura, Patrik Schatz, Sulaiman M Alsulaiman, Wael A Alsakran, Valmore A Semidey
Comparison of Posterior Hyaloid Assessment Using Preoperative Optical Coherence Tomography and Intraoperative Triamcinolone Acetonide Staining During Vitrectomy. Clinical ophthalmology (Auckland, N.Z.) 15 (2021)
Moustafa Magliyah, Abdulaziz A Alshamrani, Patrik Schatz, Ibrahim Taskintuna, Yahya Alzahrani, Sawsan R Nowilaty
Clinical spectrum, genetic associations and management outcomes of Coats-like exudative retinal vasculopathy in autosomal recessive retinitis pigmentosa. Ophthalmic genetics 42 (2) (2021)
Abdulrahman AlZaid, Moustafa S Magliyah, Patrik Schatz, Hassan Al-Dhibi
Long-term resolution of chronic macular edema after a single dose of intravitreal dexamethasone in familial retinal arterial macroaneurysm. Ophthalmic genetics 41 (4) (2020)
Ibrahim Taskintuna, Maram E A Abdalla Elsayed, Kaan Taskintuna, Khabir Ahmad, Rajiv Khandekar, Patrik Schatz, Igor Kozak
Comparison of outcomes of four different treatment modalities for diabetic vitreous haemorrhage. Scientific reports 10 (1) (2020)
Moustafa Magliyah, Hassan Al Dhibi, Patrik Schatz
Analysis of retinal function and structure in autosomal recessive retinal-renal ciliopathy. Eye (London, England) 34 (11) (2020)
Adel Salah Alahmadi, Abdulrahman H Badawi, Moustafa S Magliyah, Amani Albakri, Patrik Schatz
Poretti-Boltshauser syndrome: a rare differential diagnosis to consider in pediatric high myopia with retinal degeneration. Ophthalmic genetics 42 (1) (2020)
Moustafa Magliyah, Osama AlRaddadi, Abdullah Balbaid, Patrik Schatz
Multimodal retinal imaging in MFSD8-neuronal ceroid lipofuscinosis. Ophthalmic genetics 40 (6) (2020)
Moustafa Magliyah, Amjad Ameen Saifaldein, Patrik Schatz
Late presentation of RPE65 retinopathy in three siblings. Documenta ophthalmologica. Advances in ophthalmology 140 (3) (2020)
Faris Almutairi, Nawaf Almeshari, Khabir Ahmad, Moustafa S Magliyah, Patrik Schatz
Congenital stationary night blindness: an update and review of the disease spectrum in Saudi Arabia. Acta ophthalmologica 99 (6) (2020)
Maram E A Abdalla Elsayed, Marco Mura, Hassan Al Dhibi, Silvana Schellini, Rizwan Malik, Igor Kozak, Patrik Schatz
Sickle cell retinopathy. A focused review. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 257 (7) (2019)
Maram E A Abdalla Elsayed, Khabir Ahmad, Abdulelah A Al-Abdullah, Rizwan Malik, Rajiv Khandekar, Hernan Martinez-Osorio, Marco Mura, Patrik Schatz
Incidence of Intraocular Lens Exchange after Cataract Surgery. Scientific reports 9 (1) (2019)
Alanoud Aldrees, Ehab Abdelkader, Hussain Al-Habboubi, Huda Alrwebah, Zuhair Rahbeeni, Patrik Schatz
Non-syndromic retinal dystrophy associated with homozygous mutations in the ALMS1 gene. Ophthalmic genetics 40 (1) (2018)
Maram E A Abdalla Elsayed, Karam Hamweyah, Abdulkarim Al-Kharashi, Patrik Schatz
Multimodal imaging in serologically confirmed Rubella retinopathy. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 256 (9) (2018)
Ehab Abdelkader, Oliver Brandau, Carsten Bergmann, Nuha AlSalamah, Sawsan Nowilaty, Patrik Schatz
Novel causative variants in patients with achromatopsia. Ophthalmic genetics 39 (6) (2018)
Ehab Abdelkader, Sara AlHilali, Christine Neuhaus, Carsten Bergmann, Tahani AlMurshed, Patrik Schatz
Congenital stationary night blindness associated with morning glory disc malformation: a novel hemizygous mutation in CACNA1F. Ophthalmic genetics 39 (5) (2018)
Patrik Schatz, Ahmed Aldayel, Ibrahim Taskintuna, Ehab Abdelkader, Marco Mura
Serous retinal detachment after panretinal photocoagulation for proliferative diabetic retinopathy: a case report. Journal of medical case reports 11 (1) (2017)
Alberto Galvez-Ruiz, Anthony J Lehner, Alicia Galindo-Ferreiro, Patrik Schatz
Three New PAX2 Gene Mutations in Patients with Papillorenal Syndrome. Neuro-ophthalmology (Aeolus Press) 41 (5) (2017)
Patrik Schatz, Maram E A Abdalla Elsayed, Arif O Khan
Multimodal imaging in CABP4-related retinopathy. Ophthalmic genetics 38 (5) (2017)
Alberto Galvez-Ruiz, Alicia Galindo-Ferreiro, Patrik Schatz
Genetic Testing for Wolfram Syndrome Mutations in a Sample of 71 Patients with Hereditary Optic Neuropathy and Negative Genetic Test Results for OPA1/OPA3/LHON. Neuro-ophthalmology (Aeolus Press) 42 (2) (2017)
Patrik Schatz, Arif O Khan
Variable Familial Exudative Vitreoretinopathy in a family harbouring variants in both FZD4 and TSPAN12. Acta ophthalmologica 95 (7) (2017)
Majed Al Harbi, Rajiv Khandekar, Igor Kozak, Patrik Schatz
Association between Sickle Cell Trait and the Prevalence and Severity of Diabetic Retinopathy. PloS one 11 (7) (2016)