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American Journal of Medical Genetics. Part A|August 6, 2025
Prolonged Follow-Up in a 30-Year-Old Male With a Novel Pathogenic Variant in MSL3: A Case Report and a Brief Review of the LiteratureGiulia Pisanò, Carlo Alberto Cesaroni, Susanna Rizzi, et al.Journal of Alzheimer'S Disease : JAD|July 23, 2016
Performance Evaluation of an Automated ELISA System for Alzheimer's Disease Detection in Clinical RoutineDavide Chiasserini, Leonardo Biscetti, Lucia Farotti, et al.Tumori|April 25, 2015
Neoadjuvant chemotherapy in locally advanced gastric cancer: what to avoid. Preliminary analysis of a consecutive series of patientsStefano Rausei, Georgios D Lianos, Ilaria Proserpio, et al.Calcified Tissue International|October 3, 2003
Association between a polymorphism affecting an AP1 binding site in the promoter of the TCIRG1 gene and bone mass in womenC Sobacchi, P Vezzoni, D M Reid, et al.BMC Genomics|June 1, 2018
Distribution of ncRNAs expression across hypothalamic-pituitary-gonadal axis in Capra hircusEmanuele Capra, Barbara Lazzari, Stefano Frattini, et al.BMC Urology|September 3, 2022
Congenital cysts of the lower male genitourinary tract: a disorder with various treatment approaches and pitfalls-case reportMatteo Moretti, Davide Campobasso, Raffaele Inzillo, et al.Cancers|December 30, 2025
A Real-World Experience on the Efficacy of First-Line Treatment with Immune-Checkpoint Inhibitors in Non-Small-Cell Lung Cancer Patients with PD-L1 Expression ≥50%: The Role of <i>KRAS</i> MutationsLucia Motta, Samantha Epistolio, Jana Pankovics, et al.Journal of Clinical Medicine|July 29, 2025
Prognostic Impact of KRAS-TP53 Co-Mutations in Patients with Early-Stage Non-Small Cell Lung Cancer: A Single-Center Retrospective StudyLucia Motta, Francesca Molinari, Jana Pankovics, et al.Neurogenetics|April 23, 2024
Early-onset dysphagia and severe neurodevelopmental disorder as early signs in a patient with two novel variants in NARS1: a case report and brief review of the literatureCarlo Alberto Cesaroni, Gianluca Contrò, Carlotta Spagnoli, et al.Cell|June 18, 1998
Partial V(D)J recombination activity leads to Omenn syndromeA Villa, S Santagata, F Bozzi, et al.Pageof 80