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The Journal of Allergy and Clinical Immunology|February 16, 2016
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functionsMauro Giacomelli, Rajesh Kumar, Annarosa Soresina, et al.Blood|August 26, 2010
Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patientsLaura Tassone, Daniele Moratto, William Vermi, et al.Journal of the Neurological Sciences|November 23, 2016
Novel compound heterozygous mutations in a child with Ataxia-Telangiectasia showing unrelated cerebellar disordersMaria Piane, Anna Molinaro, Annarosa Soresina, et al.BMC Infectious Diseases|September 24, 2021
Emergence of Letermovir-resistant HCMV UL56 mutant during rescue treatment in a liver transplant recipient with ganciclovir-resistant infection HCMV: a case reportStefania Paolucci, Giulia Campanini, Irene Cassaniti, et al.Journal of Translational Medicine|September 11, 2008
Type I interferon-dependent gene MxA in perinatal HIV-infected patients under antiretroviral therapy as marker for therapy failure and blood plasmacytoid dendritic cells depletionRaffaele Badolato, Claudia Ghidini, Fabio Facchetti, et al.Clinical Immunology (Orlando, Fla.)|March 12, 2022
Lack of DOCK8 impairs the primary biologic functions of human NK cells and abrogates CCR7 surface expression in a WASP-independent mannerOrnella Patrizi, Manuela Baronio, Luisa Gazzurelli, et al.Diagnostic Cytopathology|October 7, 2019
Morphometric analysis of atypical glandular cells correctly classifies normal, reactive, and atypical cells in cervical smearsMarco Vicari, Leo Guidobaldi, Eleonora Perrella, et al.Platelets|February 8, 2022
Refractory immune thrombocytopenia successfully treated with bortezomib in a child with 22q11.2 deletion syndrome, complicated by Evans syndrome and hypogammaglobulinemiaFrancesca Conti, Francesca Gottardi, Mattia Moratti, et al.Prenatal Diagnosis|September 30, 2006
Psychological consequences of prenatal diagnosis in a case of familial Angelman syndromeDaniela Turchetti, Elisabetta Razzaboni, Hila Zomer, et al.Frontiers in Genetics|September 27, 2018
Dealing With BRCA1/2 Unclassified Variants in a Cancer Genetics Clinic: Does Cosegregation Analysis Help?Roberta Zuntini, Simona Ferrari, Elena Bonora, et al.Pageof 25