Visual electrophysiological findings in CHARGE syndrome with bilateral colobomas: a case reportHAMILTON, R; GONZALEZ, P; DUDGEON, J et al.Documenta ophthalmologica. 2010, Vol 121, Num 1, pp 63-67, issn 0012-4486, 5 p.Article

Mutation analysis of the FRAS1 gene demonstrates new mutations in a propositus with fraser syndromeSLAVOTINEK, A; LI, C; SHORR, E. H et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 18, pp 1909-1914, issn 1552-4825, 6 p.Article

Kystes de l'iris chez l'enfant. A propos de 2 casMGHAIETH, F; CHAKER, N; LIMEIM, R et al.Bulletin de la Société belge d'ophtalmologie. 2005, Num 295, pp 23-27, issn 0081-0746, 5 p.Article

Anterior coloboma with macrophthalmos and cyst MR findingsALTUN, Ersan; ARIBAL, Erkin; TOKER, Ebru et al.Clinical imaging. 2005, Vol 29, Num 6, pp 430-433, issn 0899-7071, 4 p.Article

Growth hormone deficiency (GHD): A new association in Peters' Plus Syndrome (PPS)LEE, Kuk-Wha; LEE, Phillip D. K.American journal of medical genetics. 2004, Vol 124A, Num 4, pp 388-391, issn 0148-7299, 4 p.Article

Surgical innovations in ophthalmologyGRAGOUDAS, Evangelos S; HATTON, Mark.International ophthalmology clinics. 2004, Vol 44, Num 1, issn 0020-8167, 260 p.Serial Issue

A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphylomaREDDY, M. A; FRANCIS, P. J; BERRY, V et al.British journal of ophthalmology. 2003, Vol 87, Num 2, pp 197-202, issn 0007-1161, 6 p.Article

Different expression patterns of calpain isozymes 1 and 2 (CAPN 1 and 2) in squamous cell carcinomas (SCC) and basal cell carcinomas (BCC) of human skinREICHRATH, Jörg; WELTER, Cornelius; MITSCHELE, Tanja et al.Journal of pathology. 2003, Vol 199, Num 4, pp 509-516, issn 0022-3417, 8 p.Article

Troubles visuels sans douleurHOEBEKEI, M.Louvain médical. 2003, Vol 122, Num 3, pp S103-S107, issn 0024-6956Article

Sporadic and familial blepharophimosis-ptosis-epicanthus inversus syndrome: FOXL2 mutation screen and MRI study of the superior levator eyelid muscleDOLLFUS, H; STOETZEL, C; VEILLON, F et al.Clinical genetics. 2003, Vol 63, Num 2, pp 117-120, issn 0009-9163, 4 p.Article

Trisomy 13: A rare case of congenital tarsal kinkLUCCI, Lucia M; FUKUMOTO, Walter K; ALVARENGA, Lênio S et al.Ophthalmic plastic and reconstructive surgery. 2003, Vol 19, Num 5, pp 408-410, issn 0740-9303, 3 p.Article

Die Klinik des Morning-Glory-Syndroms: Eine Falldarstellung = Morning Glory syndrome: A clinical study of two casesNAGY, Valeria; KETTESY, Beata; TOTH, Karoly et al.Klinische Monatsblätter für Augenheilkunde. 2002, Vol 219, Num 11, pp 801-805, issn 0023-2165, 5 p.Article

BRCA2 mutations in a population-based series of patients with ocular melanomaSCOW, Rodney J; VAJDIC, Claire M; ARMSTRONG, Bruce K et al.International journal of cancer. 2002, Vol 102, Num 2, pp 188-191, issn 0020-7136, 4 p.Article

Teebi hypertelorism syndrome: Report of a family with previously unrecognized findingsTSAI, Anne Chun-Hui; ROBERTSON, Jacqualyn R; TEEBI, Ahmad S et al.American journal of medical genetics. 2002, Vol 113, Num 3, pp 302-306, issn 0148-7299, 5 p.Article

The COMS randomized trial of iodine 125 brachytherapy for choroidal melanoma, II: Characteristics of patients enrolled and not enrolled: COMS Report No. 17Archives of ophthalmology (1960). 2001, Vol 119, Num 7, pp 951-965, issn 0003-9950Article

Histopathological examination of two cases of anterior staphyloma associated with Peters' anomaly and persistent hyperplastic primary vitreousMATSUBARA, Akihisa; OZEKI, Hironori; MATSUNAGA, Noriko et al.British journal of ophthalmology. 2001, Vol 85, Num 12, pp 1421-1425, issn 0007-1161Article

PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardationMALANDRINI, A; MARI, F; PALMERI, S et al.Clinical genetics. 2001, Vol 60, Num 2, pp 151-154, issn 0009-9163Article

Plaque radiation therapy for malignant melanoma of the iris and ciliary bodyFINGER, Paul T.American journal of ophthalmology. 2001, Vol 132, Num 3, pp 328-335, issn 0002-9394Article

Lymphoepitheliomalike carcinoma of the orbitAHMADI, M. Amir; PRIETO, Victor G; CLAYMAN, Gary L et al.Archives of ophthalmology (1960). 2001, Vol 119, Num 8, pp 1206-1208, issn 0003-9950Article

Hereditärer Megalophthalmus anterior: Eine genealogische Studie über 12 Patienten in vier Generationen = Megalophthalmus anterior: a genealogical essay over 12 patients in four generationsPLETZ, Claudia; HENTSCH, Rudi.Klinische Monatsblätter für Augenheilkunde. 2000, Vol 217, Num 5, pp 284-288, issn 0023-2165Article

A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15MORLE, L; BOZON, M; ZECH, J.-C et al.American journal of human genetics. 2000, Vol 67, Num 6, pp 1592-1597, issn 0002-9297Article

Decompensation of a congenital retinal macrovessel with arteriovenous communications induced by repetitive rollercoaster ridesBEATTY, Stephen; GOODALL, Karen; RADFORD, Raymond et al.American journal of ophthalmology. 2000, Vol 130, Num 4, pp 527-528, issn 0002-9394Article

Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutationsPERVEEN, R; LLOYD, I. C; WINTER, R et al.Investigative ophthalmology & visual science. 2000, Vol 41, Num 9, pp 2456-2460, issn 0146-0404Article

Syndrome de Rieger : étude clinique d'une famille et actualités génétiques = Rieger's syndrome : a familial case and geneticsCONRATH, J; HADJADJ, E; DENIS, D et al.Bulletin des sociétés d'ophtalmologie de France. 2000, Vol 100, pp 23-26, issn 0081-1270Article

Neuronal and inducible nitric oxide synthase distribution in retinas of microphthalmic miceHILBIG, H; ERNSTBERGER, J; LENK, C. A et al.Experimental and toxicologic pathology (Print). 2000, Vol 52, Num 1, pp 23-25, issn 0940-2993Article