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ophthalmology (121) 121
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1. Full Text Special issue introduction: Inherited retinal disease: Novel candidate genes, genotype-phenotype correlations, and inheritance models
by Cremers, Frans P. M and Boon, Camiel J. F and Bujakowska, Kinga and Zeitz, Christina
Genes, ISSN 2073-4425, 2018, Volume 9, Issue 4, p. 215
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Retina | Heredity | n/a
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2. Full Text Non-syndromic retinitis pigmentosa
by Verbakel, Sanne K and van Huet, Ramon A.C and Boon, Camiel J.F and den Hollander, Anneke I and Collin, Rob W.J and Klaver, Caroline C.W and Hoyng, Carel B and Roepman, Ronald and Klevering, B. Jeroen
Progress in retinal and eye research, ISSN 1350-9462, 09/2018, Volume 66, pp. 157 - 186
Phenotype | Genotype-phenotype correlation | Rod-cone dystrophy | Inherited retinal dystrophy | Retinitis pigmentosa | RP subtype | Life Sciences & Biomedicine | Ophthalmology | Science & Technology | Electroretinography | Diagnosis, Differential | Tomography, Optical Coherence | Humans | Night Blindness - diagnosis | Retinitis Pigmentosa - genetics | Genotype | Retinitis Pigmentosa - diagnosis | Vision Disorders - physiopathology | Retinitis Pigmentosa - therapy | Retinal Cone Photoreceptor Cells - pathology | Eye Proteins - genetics | Mutation | Retinal Rod Photoreceptor Cells - pathology | Diagnostic Techniques, Ophthalmological | Vision Disorders - etiology | Strategic planning (Business) | Medicine, Experimental | Medical research | Cyclic guanylic acid | Stem cells | Index Medicus
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3. Full Text The spectrum of ocular phenotypes caused by mutations in the BEST1 gene
by Boon, Camiel J.F and Klevering, B. Jeroen and Leroy, Bart P and Hoyng, Carel B and Keunen, Jan E.E and den Hollander, Anneke I
Progress in retinal and eye research, ISSN 1350-9462, 2009, Volume 28, Issue 3, pp. 187 - 205
Autosomal dominant vitreoretinochoroidopathy | Best vitelliform macular dystrophy | Bestrophin-1 | Autosomal recessive bestrophinopathy | Genotype–phenotype correlation | BEST1 | Adult-onset foveomacular vitelliform dystrophy | Genotype-phenotype correlation | Life Sciences & Biomedicine | Ophthalmology | Science & Technology | Phenotype | Animals | Eye Diseases - genetics | Ocular Physiological Phenomena - genetics | Bestrophins | Humans | Genotype | Chloride Channels - genetics | Eye Proteins - genetics | Mutation | Macular degeneration | Animal pigments | Analysis | Aquaporins | Genetic research | Genetic aspects | Neovascularization | Index Medicus
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4. Full Text Half-Dose Photodynamic Therapy versus High-Density Subthreshold Micropulse Laser Treatment in Patients with Chronic Central Serous Chorioretinopathy: The PLACE Trial
by van Dijk, Elon H. C and Fauser, Sascha and Breukink, Myrte B and Blanco-Garavito, Rocio and Groenewoud, Joannes M. M and Keunen, Jan E. E and Peters, Petrus J. H and Dijkman, Greet and Souied, Eric H and MacLaren, Robert E and Querques, Giuseppe and Downes, Susan M and Hoyng, Carel B and Boon, Camiel J. F
Ophthalmology (Rochester, Minn.), ISSN 0161-6420, 2018, Volume 125, Issue 10, pp. 1547 - 1555
Life Sciences & Biomedicine | Ophthalmology | Science & Technology | Follow-Up Studies | Central Serous Chorioretinopathy - therapy | Photochemotherapy - methods | Tomography, Optical Coherence | Humans | Middle Aged | Ophthalmoscopy | Male | Treatment Outcome | Visual Acuity | Dose-Response Relationship, Drug | Photosensitizing Agents - administration & dosage | Retinal Pigment Epithelium - pathology | Central Serous Chorioretinopathy - diagnosis | Multimodal Imaging - methods | Female | Laser Therapy - methods | Central Serous Chorioretinopathy - physiopathology | Verteporfin - administration & dosage | Choroid - pathology | Fundus Oculi | Fluorescein Angiography | Clinical trials | Photochemotherapy | Cancer | Lasers in medicine | Index Medicus
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5. Full Text Complement Factor H Gene Mutations: Implications for Genetic Testing and Precision Medicine in Macular Degeneration
by den Hollander, Anneke I and Hoyng, Carel B and Boon, Camiel J.F
Ophthalmology (Rochester, Minn.), ISSN 0161-6420, 10/2019, Volume 126, Issue 10, pp. 1422 - 1423
Life Sciences & Biomedicine | Ophthalmology | Science & Technology | Genetic Testing | Mutation | Macular Degeneration - genetics | Complement Factor H - genetics | Humans | Precision Medicine | Index Medicus
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6. Full Text Focal and Diffuse Chronic Central Serous Chorioretinopathy Treated With Half-Dose Photodynamic Therapy or Subthreshold Micropulse Laser: PLACE Trial Report No. 3
by van Rijssen, Thomas J and van Dijk, Elon H.C and Scholz, Paula and Breukink, Myrte B and Blanco-Garavito, Rocio and Souied, Eric H and Keunen, Jan E.E and MacLaren, Robert E and Querques, Giuseppe and Fauser, Sascha and Downes, Susan M and Hoyng, Carel B and Boon, Camiel J.F
American journal of ophthalmology, ISSN 0002-9394, 09/2019, Volume 205, pp. 1 - 10
Life Sciences & Biomedicine | Ophthalmology | Science & Technology | Follow-Up Studies | Photosensitizing Agents - therapeutic use | Photochemotherapy - methods | Tomography, Optical Coherence | Humans | Middle Aged | Central Serous Chorioretinopathy - drug therapy | Male | Treatment Outcome | Visual Acuity | Time Factors | Central Serous Chorioretinopathy - diagnosis | Lasers | Female | Retrospective Studies | Verteporfin - therapeutic use | Choroid - pathology | Chronic Disease | Fundus Oculi | Retina - pathology | Fluorescein Angiography | Clinical trials | Photochemotherapy | Analysis | Fluorescein | Cancer | Photodynamic therapy | Medical imaging | Eye diseases | Retina | Evidence-based medicine | Index Medicus | Abridged Index Medicus
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