Patrik Schatz
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- 2020
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Mark
Rhegmatogenous Retinal Detachment in Nonsyndromic High Myopia Associated with Recessive Mutations in LRPAP1
(
- Contribution to journal › Published meeting abstract
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Mark
Severe retinitis pigmentosa phenotype associated with novel CNGB1 variants
(
- Contribution to journal › Article
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Mark
Long-term resolution of chronic macular edema after a single dose of intravitreal dexamethasone in familial retinal arterial macroaneurysm
(
- Contribution to journal › Letter
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Mark
DIFFUSE RETINAL VASCULAR LEAKAGE AND CONE-ROD DYSTROPHY IN A FAMILY WITH THE HOMOZYGOUS MISSENSE C.1429G>A (P.GLY477ARG) MUTATION IN CRB1
(
- Contribution to journal › Article
- 2019
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Mark
Non-syndromic retinal dystrophy associated with homozygous mutations in the ALMS1 gene
(
- Contribution to journal › Letter
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Mark
Sickle cell retinopathy. A focused review
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- Contribution to journal › Scientific review
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Mark
Accommodative esotropia and Brown syndrome in a girl with recessive geleophysic dysplasia
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- Contribution to journal › Article
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Mark
Multimodal retinal imaging in MFSD8-neuronal ceroid lipofuscinosis
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- Contribution to journal › Letter
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Mark
Long-term follow-up of retinal function and structure in trpm1-associated complete congenital stationary night blindness
(
- Contribution to journal › Article
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Mark
Incidence of Intraocular Lens Exchange after Cataract Surgery
(
- Contribution to journal › Article