Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Kidney & Blood Pressure Research|June 9, 2021
Results of a Gene Panel Approach in a Cohort of Patients with Incomplete Distal Renal Tubular Acidosis and NephrolithiasisViola D'Ambrosio, Alessia Azzarà, Eugenio Sangiorgi, et al.
Mutation Research|April 7, 2016
Vincristine-induced bystander effect in human lymphocytesSerena Testi, Alessia Azzarà, Caterina Giovannini, et al.
Molecular Syndromology|June 8, 2017
Maternal Uniparental Disomy 14 (Temple Syndrome) as a Result of a Robertsonian TranslocationVeronica Bertini, Antonella Fogli, Rossella Bruno, et al.
Biology|November 11, 2022
Genetic Characterization in Familial Rotator Cuff Tear: An Exome Sequencing StudyAlessia Azzarà, Laura Risi Ambrogioni, Ilaria Cassano, et al.
Frontiers in Pediatrics|April 6, 2017
A Case of 22q11 Deletion Syndrome (22q11DS) with a Panayiotopoulos Epileptic Pattern: Are Additional Copy-Number Variations a Possible Second Hit in Modulating the 22q11DS Phenotype?Veronica Bertini, Angelo Valetto, Alessia Azzarà, et al.
European Journal of Neurology|October 12, 2023
A new gene for autosomal dominant facial palsy/migraine identified in a family by whole exome sequencingAlessia Azzarà, Ilaria Cassano, Carla Lintas, et al.
Genes|December 23, 2022
Expanding the Spectrum of KDM5C Neurodevelopmental Disorder: A Novel De Novo Stop Variant in a Young Woman and Emerging Genotype-Phenotype CorrelationsCarla Lintas, Irene Bottillo, Roberto Sacco, et al.
Gene Reports|November 9, 2022
Whole exome sequencing identifies a rare variant in MAS1 gene in a subject with lethal COVID-19Alessia Azzarà, Ilaria Cassano, Maria Cristina Tirindelli, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|April 15, 2021
Identification of new candidate genes for spina bifida through exome sequencingAlessia Azzarà, Claudia Rendeli, Anna Maria Crivello, et al.
Mutation Research. Reviews in Mutation Research|March 21, 2020
Role of oxidative stress, genome damage and DNA methylation as determinants of pathological conditions in the newborn: an overview from conception to early neonatal stageRoberto Scarpato, Serena Testi, Valentina Colosimo, et al.
Pageof 3