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BMC Bioinformatics|June 30, 2017
SLMSuite: a suite of algorithms for segmenting genomic profilesValerio Orlandini, Aldesia Provenzano, Sabrina Giglio, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 15, 2010
Growth hormone therapy-related hyperglycaemia in a boy with renal cystic hypodysplasia and a new mutation of the HNF1 beta geneSabrina Giglio, Elisa Contini, Sonia Toni, et al.Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|February 14, 2019
[A child with severe growth delay and renal cysts]Gianluca Vergine, Elisa Ravaioli, Viviana Palazzo, et al.Journal of Nephrology|March 26, 2021
Distal renal tubular acidosis: a systematic approach from diagnosis to treatmentSabrina Giglio, Giovanni Montini, Francesco Trepiccione, et al.Clinical and Translational Science|September 29, 2025
Risk and Association of Specific HLA Alleles With Nintedanib-Induced Gastrointestinal Adverse Reactions: A Discovery Study in an Italian PopulationStefano Mocci, Roberto Littera, Silvia Deidda, et al.Molecular Genetics & Genomic Medicine|December 19, 2020
RB1CC1 duplication and aberrant overexpression in a patient with schizophrenia: further phenotype delineation and proposal of a pathogenetic mechanismEdoardo Errichiello, Roberto Giorda, Antonella Gambale, et al.Journal of Nephrology|May 23, 2016
Lessons from genetics: is it time to revise the therapeutic approach to children with steroid-resistant nephrotic syndrome?Francesca Becherucci, Benedetta Mazzinghi, Aldesia Provenzano, et al.The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|October 28, 2014
Prevalence and prenatal ultrasound detection of clubfoot in a non-selected population: an analysis of 549, 931 births in TuscanyViola Seravalli, Anna Pierini, Fabrizio Bianchi, et al.European Journal of Medical Genetics|March 14, 2017
Chiari I malformation in a child with PTEN hamartoma tumor syndrome: Association or coincidence?Veronica Saletti, Silvia Esposito, Angelo Maccaro, et al.Cytogenetic and Genome Research|February 9, 2023
Heterozygous Deletion of Long Noncoding RNA AK127244 Is a Susceptibility Factor for Neurodevelopmental DelayEmanuele G Coci, Ornella Galesi, Thomas Morgan, et al.Pageof 11