Showing results (271-280 of 621) with videos related to
Sort By:
Pageof 63
Frontiers in Genetics|December 20, 2021
Spondyloocular Syndrome: A Novel XYLT2 Variant with Description of the Neonatal PhenotypeGabriella Doddato, Alessandra Fabbiani, Chiara Fallerini, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 28, 2015
Antiepileptic drugs in Rett SyndromeMaria Pintaudi, Maria Grazia Calevo, Aglaia Vignoli, et al.European Journal of Human Genetics : EJHG|May 14, 2015
Altered expression of neuropeptides in FoxG1-null heterozygous mutant miceElisa Frullanti, Sonia Amabile, Maria Grazia Lolli, et al.Cancer Research and Treatment|May 27, 2017
Omic Approach in Non-smoker Female with Lung Squamous Cell Carcinoma Pinpoints to Germline Susceptibility and Personalized MedicineMargherita Baldassarri, Chiara Fallerini, Francesco Cetta, et al.Frontiers in Genetics|September 4, 2023
Case report: PIK3CA somatic mutation leading to Klippel Trenaunay Syndrome and multiple tumorsViola Bianca Serio, Maria Palmieri, Simona Innamorato, et al.Cells|December 23, 2022
Gain- and Loss-of-Function CFTR Alleles Are Associated with COVID-19 Clinical OutcomesMargherita Baldassarri, Kristina Zguro, Valeria Tomati, et al.Toxics|August 12, 2018
Oxidative Stress in Methylmercury-Induced Cell ToxicityAlessandra Antunes Dos Santos, Beatriz Ferrer, Filipe Marques Gonçalves, et al.Neuroscience|January 27, 2009
The XLMR gene ACSL4 plays a role in dendritic spine architectureI Meloni, V Parri, R De Filippis, et al.Frontiers in Pediatrics|April 27, 2026
Novel NFIX variant in a patient with Malan syndrome and associated Chiari type I malformation: a case reportMichele Minerva, Anna Maria Pinto, Filippo Toninelli, et al.Journal of Neurology|November 14, 2009
The first Italian family with tibial muscular dystrophy caused by a novel titin mutationMarzia Pollazzon, Tiina Suominen, Sini Penttilä, et al.Pageof 63