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Diabetes & Metabolism|January 3, 2012
Consensus statement on the care of the hyperglycaemic/diabetic patient during and in the immediate follow-up of acute coronary syndromeB Vergès, A Avignon, F Bonnet, et al.Archives of Cardiovascular Diseases|July 19, 2012
Consensus statement on the care of the hyperglycaemic/diabetic patient during and in the immediate follow-up of acute coronary syndromeB Vergès, A Avignon, F Bonnet, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 8, 2008
[Recommendations for the management of bone demineralization in cystic fibrosis]I Sermet-Gaudelus, R Nove-Josserand, G-A Loeille, et al.American Journal of Human Genetics|January 25, 2024
Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunctionMiriam Bauwens, Elifnaz Celik, Dinah Zur, et al.American Journal of Human Genetics|February 26, 2026
Loss-of-function variants in SAXO6, encoding a microtubule inner protein of photoreceptor cilia, causes a late-onset retinal dystrophyAbigail R Moye, Caitlyn L McCafferty, Siying Lin, et al.American Journal of Human Genetics|September 3, 2016
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia DefectsKonstantinos Nikopoulos, Pietro Farinelli, Basilio Giangreco, et al.Investigative Ophthalmology & Visual Science|April 4, 2024
The Pediatric and Young Adult Choroidal and Ciliary Body Melanoma Genetic Study, A Survey by the European Ophthalmic Oncology GroupNatasha M van Poppelen, Nathalie Cassoux, Joni A Turunen, et al.American Journal of Human Genetics|March 13, 2025
Bi-allelic variants in three genes encoding distinct subunits of the vesicular AP-5 complex cause hereditary macular dystrophyKarolina Kaminska, Francesca Cancellieri, Mathieu Quinodoz, et al.Pageof 25