Schatz P - Search Results

1

Rhegmatogenous Retinal Detachment in Nonsyndromic High Myopia Associated with Recessive Mutations in LRPAP1.

Magliyah MS, Alsulaiman SM, Nowilaty SR, Alkuraya FS, Schatz P. Magliyah MS, et al. Among authors: schatz p. Ophthalmol Retina. 2020 Jan;4(1):77-83. doi: 10.1016/j.oret.2019.08.005. Epub 2019 Aug 22. Ophthalmol Retina. 2020. PMID: 31607522

2

Retinal function after scleral buckling for recent onset rhegmatogenous retinal detachment: assessment with electroretinography and optical coherence tomography.

Schatz P, Holm K, Andréasson S. Schatz P, et al. Retina. 2007 Jan;27(1):30-6. doi: 10.1097/01.iae.0000256659.71864.83. Retina. 2007. PMID: 17218912

3

Recovery of retinal function after recent-onset rhegmatogenous retinal detachment in relation to type of surgery.

Schatz P, Andréasson S. Schatz P, et al. Retina. 2010 Jan;30(1):152-9. doi: 10.1097/IAE.0b013e3181b32ed4. Retina. 2010. PMID: 19940806

4

Fundus albipunctatus associated with compound heterozygous mutations in RPE65.

Schatz P, Preising M, Lorenz B, Sander B, Larsen M, Rosenberg T. Schatz P, et al. Ophthalmology. 2011 May;118(5):888-94. doi: 10.1016/j.ophtha.2010.09.005. Epub 2011 Jan 6. Ophthalmology. 2011. PMID: 21211845

5

DIFFUSE RETINAL VASCULAR LEAKAGE AND CONE-ROD DYSTROPHY IN A FAMILY WITH THE HOMOZYGOUS MISSENSE C.1429G>A (P.GLY477ARG) MUTATION IN CRB1.

Alsulaiman HM, Schatz P, Nowilaty SR, Abdelkader E, Abu Safieh L. Alsulaiman HM, et al. Among authors: schatz p. Retin Cases Brief Rep. 2020 Spring;14(2):203-210. doi: 10.1097/ICB.0000000000000654. Retin Cases Brief Rep. 2020. PMID: 29200130

6

Novel causative variants in patients with achromatopsia.

Abdelkader E, Brandau O, Bergmann C, AlSalamah N, Nowilaty S, Schatz P. Abdelkader E, et al. Among authors: schatz p. Ophthalmic Genet. 2018 Dec;39(6):678-683. doi: 10.1080/13816810.2018.1522653. Epub 2018 Oct 5. Ophthalmic Genet. 2018. PMID: 30289319

7

Multimodal retinal imaging in MFSD8-neuronal ceroid lipofuscinosis.

Magliyah M, AlRaddadi O, Balbaid A, Schatz P. Magliyah M, et al. Among authors: schatz p. Ophthalmic Genet. 2019 Dec;40(6):588-590. doi: 10.1080/13816810.2019.1709125. Epub 2020 Jan 7. Ophthalmic Genet. 2019. PMID: 31909682 No abstract available.

8

Analysis of retinal function and structure in autosomal recessive retinal-renal ciliopathy.

Magliyah M, Al Dhibi H, Schatz P. Magliyah M, et al. Among authors: schatz p. Eye (Lond). 2020 Nov;34(11):2135-2137. doi: 10.1038/s41433-019-0754-y. Epub 2020 Jan 7. Eye (Lond). 2020. PMID: 31911653 Free PMC article. No abstract available.

9

Late presentation of RPE65 retinopathy in three siblings.

Magliyah M, Saifaldein AA, Schatz P. Magliyah M, et al. Among authors: schatz p. Doc Ophthalmol. 2020 Jun;140(3):289-297. doi: 10.1007/s10633-019-09745-z. Epub 2020 Jan 10. Doc Ophthalmol. 2020. PMID: 31925606 Free PMC article.

10

Analysis of retinal structure and function in cone dystrophy with supernormal rod response.

Abdelkader E, Yasir ZH, Khan AM, Raddadi O, Khandekar R, Alateeq N, Nowilaty S, AlShahrani N, Schatz P. Abdelkader E, et al. Among authors: schatz p. Doc Ophthalmol. 2020 Aug;141(1):23-32. doi: 10.1007/s10633-020-09748-1. Epub 2020 Jan 20. Doc Ophthalmol. 2020. PMID: 31960170

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