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European Journal of Medical Genetics|March 24, 2009
14q12 Microdeletion syndrome and congenital variant of Rett syndromeMaria Antonietta Mencarelli, Tjitske Kleefstra, Eleni Katzaki, et al.European Journal of Ophthalmology|April 17, 2012
13q deletion syndrome and retinoblastoma in identical dichorionic diamniotic monozygotic twinsSonia De Francesco, Paolo Galluzzi, Alessandra Del Longo, et al.Cancer Cell International|November 2, 2019
PIK3CA-CDKN2A clonal evolution in metastatic breast cancer and multiple points cell-free DNA analysisMaria Palmieri, Margherita Baldassarri, Francesca Fava, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 23, 2022
A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosisDiego Lopergolo, Gianna Berti, Francesca Mari, et al.The EMBO Journal|April 8, 2014
Capping of the N-terminus of PSD-95 by calmodulin triggers its postsynaptic releaseYonghong Zhang, Lucas Matt, Tommaso Patriarchi, et al.European Journal of Medical Genetics|March 28, 2009
A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumbM Pollazzon, S Grosso, F T Papa, et al.Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|March 22, 2020
Multiresidue analysis of insecticides and fungicides in apples from the Greek market. Applying an alternative approach for risk assessmentManolis Tzatzarakis, Manolis Kokkinakis, Elisavet Renieri, et al.Age (Dordrecht, Netherlands)|April 29, 2014
Effects of zinc-fortified drinking skim milk (as functional food) on cytokine release and thymic hormone activity in very old persons: a pilot studyLaura Costarelli, Robertina Giacconi, Marco Malavolta, et al.Journal of Neuroradiology = Journal De Neuroradiologie|June 20, 2018
Bail-out intracranial stenting with Solitaire AB device after unsuccessful thrombectomy in acute ischemic stroke of anterior circulationSergio Nappini, Nicola Limbucci, Giuseppe Leone, et al.Clinical Genetics|September 13, 2001
PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardationA Malandrini, F Mari, S Palmeri, et al.Pageof 63