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Mutation Research|May 15, 2017
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari familiesMoza K Alkowari, Diego Vozzi, Shruti Bhagat, et al.
JACC. Advances|July 28, 2026
Arrhythmic Risk in Carriers of Predicted Deleterious Rare Variants in Dilated and Arrhythmogenic Cardiomyopathy GenesIlaria Gandin, Andrea Mario Vergani, Michela Carlotta Massi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2014
Excess of runs of homozygosity is associated with severe cognitive impairment in intellectual disabilityIlaria Gandin, Flavio Faletra, Francesca Faletra, et al.
Sarcoidosis, Vasculitis, and Diffuse Lung Diseases : Official Journal of WASOG|December 15, 2025
Exploring sarcoidosis via nailfold capillaroscopy: A window into the disease's microvascular landscapeLucrezia Mondini, Mariangela Barbieri, Liliana Trotta, et al.
Journal of Clinical Medicine|August 14, 2025
Evaluation of Nailfold Capillaroscopy as a Novel Tool in the Assessment of Eosinophilic Granulomatosis with PolyangiitisGianluca Screm, Ilaria Gandin, Lucrezia Mondini, et al.
Mutation Research|September 29, 2015
Target sequencing approach intended to discover new mutations in non-syndromic intellectual disabilityAnna Morgan, Ilaria Gandin, Chiara Belcaro, et al.
European Journal of Heart Failure|August 15, 2025
Clustering in dilated cardiomyopathy at initial evaluation: An effective tool for clinical stratificationIlaria Gandin, Maria Perotto, Alessia Paldino, et al.
European Journal of Human Genetics : EJHG|December 1, 2019
A bird's-eye view of Italian genomic variation through whole-genome sequencingMassimiliano Cocca, Caterina Barbieri, Maria Pina Concas, et al.
Diagnostics (Basel, Switzerland)|September 28, 2023
Pulmonary Sarcoidosis and Immune Dysregulation: A Pilot Study on Possible CorrelationRossella Cifaldi, Francesco Salton, Paola Confalonieri, et al.
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