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International Journal of Molecular Sciences|April 30, 2021
Exosomes from Plasma of Neuroblastoma Patients Contain Doublestranded DNA Reflecting the Mutational Status of Parental Tumor CellsChiara Degli Esposti, Barbara Iadarola, Simone Maestri, et al.European Journal of Medical Genetics|June 29, 2011
A de novo balanced translocation t(7;12)(p21.2;p12.3) in a patient with Saethre-Chotzen-like phenotype downregulates TWIST and an osteoclastic protein-tyrosine phosphatase, PTP-ocPatrizia De Marco, Alessandro Raso, Silvana Beri, et al.Vaccines|September 28, 2024
Characterization of the Monkeypox Virus [MPX]-Specific Immune Response in MPX-Cured Individuals Using Whole Blood to Monitor Memory ResponseElisa Petruccioli, Settimia Sbarra, Serena Vita, et al.Molecular Cytogenetics|May 27, 2014
Constitutional chromosomal events at 22q11 and 15q26 in a child with a pilocytic astrocytoma of the spinal cordSamantha Mascelli, Mariasavina Severino, Alessandro Raso, et al.Neuroradiology|November 1, 2019
Role of diffusion weighted imaging for differentiating cerebral pilocytic astrocytoma and ganglioglioma BRAF V600E-mutant from wild typeAntonia Ramaglia, Domenico Tortora, Kshitij Mankad, et al.BMC Pediatrics|November 29, 2022
Early molecular diagnosis of BRAF status drives the neurosurgical management in BRAF V600E-mutant pediatric low-grade gliomas: a case reportGianluca Piccolo, Antonio Verrico, Giovanni Morana, et al.Frontiers in Genetics|April 22, 2025
Arteriovenous cerebral high-flow shunts: genetic analysis of patients from a pediatric tertiary care centerFerruccio Romano, Patrizia De Marco, Giulia Amico, et al.The New England Journal of Medicine|April 6, 2007
Mutations in VANGL1 associated with neural-tube defectsZoha Kibar, Elena Torban, Jonathan R McDearmid, et al.Molecular Genetics & Genomic Medicine|November 12, 2018
Whole exome sequencing identifies novel predisposing genes in neural tube defectsPhilippe Lemay, Patrizia De Marco, Monica Traverso, et al.BMC Medical Genetics|December 24, 2016
Sacral agenesis: a pilot whole exome sequencing and copy number studyRobert M Porsch, Elisa Merello, Patrizia De Marco, et al.Pageof 10