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BMJ Case Reports|November 14, 2023
Atypical hypertrophy of retinal pigment epithelium manifesting as the first sign of familial adenomatous polyposisJoão Ponces Ramalhão, Miguel Afonso, Mafalda Macedo, et al.Ophthalmic Surgery, Lasers & Imaging Retina|April 4, 2014
Multimodal imaging of exudative maculopathy associated with hand-foot-mouth diseaseSara Vaz-Pereira, Mafalda Macedo, Gabriella De Salvo, et al.Journal of Family & Reproductive Health|August 7, 2023
Raynaud Phenomenon of the Nipple: A Clinical Case ReportCarolina Quental, Daniel Bertoluci Brito, João Sobral, et al.Case Reports in Ophthalmological Medicine|January 30, 2015
Purtscher-like retinopathyRita Massa, Carolina Vale, Mafalda Macedo, et al.Clinical Genetics|September 3, 2021
Novel KMT2B mutation causes cerebellar ataxia: Expanding the clinical phenotypeJoana Damásio, Mariana Santos, Raquel Samões, et al.Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|March 8, 2023
Application of optical coherence tomography angiography for microvascular changes in patients treated with hydroxychloroquine: a systematic review and meta-analysisAndré Ferreira, Rita Anjos, Rafael José-Vieira, et al.ARP Rheumatology|May 28, 2022
The 2021 Portuguese Society of Ophthalmology joint guidelines with Paediatric Rheumatology on the screening, monitoring and medical treatment of juvenile idiopathic arthritis-associated uveitisInês Leal, Vasco Miranda, Cristina Fonseca, et al.Pageof 1