H. Tran

发表

Primary choroidal melanoma in phakomatosis pigmentovascularis IIa.

L. Zografos, H. Tran, 2005, Ophthalmology.

High-frequency ultrasonographic evaluation of conjunctival intraepithelial neoplasia and squamous cell carcinoma.

R. Ritch, P. Finger, D. Abramson, 2003, Archives of ophthalmology.

Subfoveal nodule in Coats disease: towards an updated classification predicting visual prognosis

F. Munier, A. Matet, A. Moulin, 2017 .

Ultrasound biomicroscopy in uveitis-glaucoma-hyphema syndrome.

H. Ishikawa, R. Ritch, J. Liebmann, 2002, American journal of ophthalmology.

Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis

A. Hoischen, C. Rivolta, P. Farinelli, 2022, Frontiers in Cell and Developmental Biology.

Bilateral circumscribed choroidal hemangioma in an otherwise healthy individual.

L. Zografos, A. Schalenbourg, H. Tran, 2007, Retinal cases & brief reports.

Leber Congenital Amaurosis Associated with AIPL1: Challenges in Ascribing Disease Causation, Clinical Findings, and Implications for Gene Therapy

Dorothy A. Thompson, R. MacLaren, M. Michaelides, 2012, PloS one.

Differential Dimerization of Variants Linked to Enhanced S‐Cone Sensitivity Syndrome (ESCS) Located in the NR2E3 Ligand‐Binding Domain

N. Guex, D. Alpen, D. Schorderet, 2015, Human mutation.

Iridociliary apposition in plateau iris syndrome persists after cataract extraction.

R. Ritch, J. Liebmann, H. V. Tran, 2002, American journal of ophthalmology.

Persistence of increased Eotaxin-1 (CCL11) level in tears of patients wearing contact lenses: a long-term follow-up study.

S. Eperon, Y. Guex-Crosier, H. Tran, 2011, Klinische Monatsblätter für Augenheilkunde.

Ultrasound biomicroscopic assessment of zonular appearance in exfoliation syndrome.

Hiroshi Ishikawa, Robert Ritch, Roberto M Vessani, 2007, Acta ophthalmologica Scandinavica.

Angle closure: classification, concepts, and the role of ultrasound biomicroscopy in diagnosis and treatment

R. Ritch, J. Liebmann, C. Tello, 2002, Seminars in ophthalmology.

In vivo study comparing an X‐shaped polymethylmethacrylate and a cylindrical collagen implant for deep sclerectomy

A. Mermoud, K. Mansouri, C. Schnyder, 2011, Clinical & experimental ophthalmology.

Peripapillary choroidal neovascularization associated with melanocytoma of the optic disc: a clinicopathologic case report

S. Uffer, L. Zografos, E. Bovey, 2006, Graefe's Archive for Clinical and Experimental Ophthalmology.

Comparing Deep Sclerectomy With Collagen Implant to the New Method of Very Deep Sclerectomy With Collagen Implant: A Single-masked Randomized Controlled Trial

A. Mermoud, K. Mansouri, E. Ravinet, 2010, Journal of glaucoma.

Retinal Structure in RPE65-Associated Retinal Dystrophy

M. Larsen, M. Michaelides, J. Bainbridge, 2020, Investigative ophthalmology & visual science.

Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectors.

Mark Basche, Jenny McIntosh, Tiansen Li, 2009, Human molecular genetics.

SUBFOVEAL NODULE IN COATS' DISEASE

F. Munier, H. V. Tran, A. Matet, 2017, Retina.

PATTERN DYSTROPHY WITH HIGH INTRAFAMILIAL VARIABILITY ASSOCIATED WITH Y141C MUTATION IN THE PERIPHERIN/RDS GENE AND SUCCESSFUL TREATMENT OF SUBFOVEAL CNV RELATED TO MULTIFOCAL PATTERN TYPE WITH ANTI-VEGF (RANIBIZUMAB) INTRAVITREAL INJECTIONS

D. Schorderet, F. Munier, V. Vaclavik, 2012, Retina.

Novel PDE6B Mutation Presenting with Retinitis Pigmentosa – A Case Series of Three Patients

K. Stingl, D. Schorderet, A. Palmowski-Wolfe, 2019, Klinische Monatsblätter für Augenheilkunde.

Novel PDE 6 B Mutation Presenting with Retinitis Pigmentosa – A Case Series of Three Patients Neue PDE 6 B-Mutation bei Retinitis pigmentosa – 3 Fallberichte

K. Stingl, D. Schorderet, A. Palmowski-Wolfe, 2019 .

Posterior Sub-Tenon Triamcinolone Injection for Chronic Macular Oedema Associated With Non-Ischemic Branch or Central Retinal Vein Occlusion

J. Pournaras, T. Wolfensberger, A. Ambresin, 2016 .

Double concentric autofluorescence ring in NR2E3-p.G56R-linked autosomal dominant retinitis pigmentosa.

D. Schorderet, F. Munier, V. Vaclavik, 2012, Investigative ophthalmology & visual science.

Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy Efficacy

C. Kostic, D. Sharon, Y. Arsenijévic, 2021, International journal of molecular sciences.

Autofluorescence Lifetimes in Patients With Choroideremia Identify Photoreceptors in Areas With Retinal Pigment Epithelium Atrophy.

S. Wolf, M. Zinkernagel, Chantal Dysli, 2016, Investigative ophthalmology & visual science.

Different Phenotypes in Pseudodominant Inherited Retinal Dystrophies

D. Schorderet, H. V. Tran, L. el Matri, 2021, Frontiers in Cell and Developmental Biology.

Blood-brain barrier disruption associated with topiramate-induced angle-closure glaucoma of acute onset.

M. Reichhart, C. Schnyder, Y. Guex-Crosier, 2006, Klinische Monatsblatter fur Augenheilkunde.

Swiss Family with Dominant Stargardt Disease Caused by a Recurrent Mutation in the ELOVL4 Gene

D. Schorderet, F. Munier, V. Vaclavik, 2016, Klin Monatsbl Augenheilkd.

Risk assessment of recurrence in sporadic retinoblastoma using a molecular-based algorithm

D. Schorderet, F. Munier, M. Gaillard, 2012, Ophthalmic genetics.