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Journal of Medical Genetics|December 30, 2023
Clinical implications of VUS reclassification in a single-centre series from application of ACMG/AMP classification rules specified for BRCA1/2Giovanni Innella, Simona Ferrari, Sara Miccoli, et al.The Journal of General Virology|April 15, 2003
Nucleotide variation in Sabin type 2 poliovirus from an immunodeficient patient with poliomyelitisGabriele Buttinelli, Valentina Donati, Stefano Fiore, et al.The Journal of Pediatrics|July 22, 2008
Sensorineural hearing loss in primary antibody deficiency disordersMarco Berlucchi, Annarosa Soresina, Luca O Redaelli De Zinis, et al.Frontiers in Immunology|November 23, 2020
Case Report: A Case of X-Linked Agammaglobulinemia With High Serum IgE Levels and Allergic RhinitisBianca Cinicola, Andrea Uva, Lucia Leonardi, et al.Journal of Immunology Research|April 29, 2016
Clinical Associations of Biallelic and Monoallelic TNFRSF13B Variants in Italian Primary Antibody Deficiency SyndromesFederica Pulvirenti, Roberta Zuntini, Cinzia Milito, et al.Clinical Immunology (Orlando, Fla.)|September 12, 2006
Combined decrease of defined B and T cell subsets in a group of common variable immunodeficiency patientsDaniele Moratto, Anna Virginia Gulino, Stefania Fontana, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|November 13, 2010
Inherited human gp91phox deficiency is associated with impaired isoprostane formation and platelet dysfunctionPasquale Pignatelli, Roberto Carnevale, Serena Di Santo, et al.AIDS (London, England)|August 15, 2014
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activityCinzia Giagulli, Francesca Caccuri, Francesca Cignarella, et al.Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|June 17, 2016
Molecular detection and genetic characterization of circulating measles virus in northern ItalyGiulia Piccirilli, Angela Chiereghin, Maria Grazia Pascucci, et al.Clinical Chemistry|January 20, 2007
Simple method for haplotyping the poly(TG) repeat in individuals carrying the IVS8 5T allele in the CFTR geneVilma Mantovani, Paolo Garagnani, Paola Selva, et al.Pageof 25