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Expert Review of Clinical Immunology|April 2, 2014
Rheumatoid arthritis and the biological clockAngelo De Cata, Leonardo D'Agruma, Roberto Tarquini, et al.
Acta Bio-Medica : Atenei Parmensis|November 10, 2020
Genetic analysis of genes associated with epilepsyGiulia Guerri, Marco Castori, Leonardo D'Agruma, et al.
Neurosurgery|May 28, 2005
Hemangioblastomas of central nervous system: molecular genetic analysis and clinical managementDomenico Catapano, Lucia Anna Muscarella, Vito Guarnieri, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 19, 2018
Leber's hereditary optic neuropathy (LHON) in an Apulian cohort of subjectsAngelica Bianco, Luigi Bisceglia, Paolo Trerotoli, et al.
Oxidative Medicine and Cellular Longevity|February 8, 2019
A Nonsense Mitochondrial DNA Mutation Associates with Dysfunction of HIF1α in a Von Hippel-Lindau Renal OncocytomaMonica De Luise, Vito Guarnieri, Claudio Ceccarelli, et al.
American Journal of Medical Genetics. Part A|March 18, 2025
Hereditary Multiple Osteochondromas and Acute Lymphoblastic Leukemia: A Possible Role for EXT1 and EXT2 in Hematopoietic MalignanciesFrancesco Comisi, Carmela Fusco, Rosamaria Mura, et al.
Journal of Human Genetics|April 18, 2007
An 11-bp duplication in the promoter region of the VHL gene in a patient with cerebellar hemangioblastoma and renal oncocytomaLucia Anna Muscarella, Raffaela Barbano, Bartolomeo Augello, et al.
Investigative Ophthalmology & Visual Science|April 14, 2017
High Mitochondrial DNA Copy Number Is a Protective Factor From Vision Loss in Heteroplasmic Leber's Hereditary Optic Neuropathy (LHON)Angelica Bianco, Luigi Bisceglia, Luciana Russo, et al.
Journal of Biomedicine & Biotechnology|February 11, 2010
VHL frameshift mutation as target of nonsense-mediated mRNA decay in Drosophila melanogaster and human HEK293 cell lineLucia Micale, Lucia Anna Muscarella, Marco Marzulli, et al.
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