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BMJ Case Reports|June 7, 2018
Gitelman syndrome and primary hyperparathyroidism: a rare associationTeresa Rego, Fernando Fonseca, Rita Cerqueira, et al.International Journal of Molecular Sciences|July 27, 2024
Development and Characterization of Curcumin-Loaded TPGS/F127/P123 Polymeric Micelles as a Potential Therapy for Colorectal CancerRita Cerqueira, Cátia Domingues, Francisco Veiga, et al.European Journal of Medical Genetics|March 15, 2011
Novel deletion encompassing exons 5-12 of the UBE3A gene in a girl with Angelman syndromeAna Beleza-Meireles, Rita Cerqueira, Sérgio B Sousa, et al.Acta Medica Portuguesa|August 19, 2009
[Hereditary pancreatitis in a child]Sílvia Freira, Teresa Lourenço, Rita Cerqueira, et al.European Journal of Dermatology : EJD|May 16, 2009
Epidermolytic hyperkeratosis with palmoplantar keratoderma in a patient with KRT10 mutationPaulo Morais, Alberto Mota, Teresa Baudrier, et al.BMC Medical Education|July 27, 2023
Visual Thinking Strategies in medical education: a systematic reviewAna Rita Cerqueira, Ana Sofia Alves, Matilde Monteiro-Soares, et al.Dermatology Online Journal|February 5, 2013
Piebaldism and neurofibromatosis: state of knowledgeAna Duarte, Alberto Mota, Teresa Baudrier, et al.Dermatology Online Journal|February 9, 2010
Piebaldism and neurofibromatosis type 1: family reportAna Filipa Duarte, Alberto Mota, Teresa Baudrier, et al.Photodiagnosis and Photodynamic Therapy|February 25, 2021
Long term outer retinal changes in central serous chorioretinopathy submitted to half-dose photodynamic therapySónia Torres-Costa, Susana Penas, Ana Rita Cerqueira, et al.European Journal of Dermatology : EJD|June 11, 2011
Erythropoietic protoporphyria: a family study and report of a novel mutation in the FECH genePaulo Morais, Alberto Mota, Teresa Baudrier, et al.Pageof 2