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Interventional Neuroradiology : Journal of Peritherapeutic Neuroradiology, Surgical Procedures and Related Neurosciences|May 23, 2013
Effects of hyper-early (<12 hours) endovascular treatment of ruptured intracranial aneurysms on clinical outcomeA Consoli, G Grazzini, L Renieri, et al.Human Genetics|October 1, 1993
Small frameshift deletions within the COL4A5 gene in juvenile-onset Alport syndromeA Renieri, M Seri, L Galli, et al.Transplantation|January 3, 2020
Detection of Cryptic Mosaicism in X-linked Alport Syndrome Prompts to Re-evaluate Living-donor Kidney TransplantationAnna Maria Pinto, Sergio Daga, Chiara Fallerini, et al.Nature Communications|August 15, 2019
A glomerulus-on-a-chip to recapitulate the human glomerular filtration barrierAstgik Petrosyan, Paolo Cravedi, Valentina Villani, et al.Nephron|January 1, 1995
Renal transplantation from living donor parents in two brothers with Alport syndrome. Can asymptomatic female carriers of the Alport gene be accepted as kidney donors?A Sessa, A Pietrucci, S Carozzi, et al.Clinical Genetics|June 6, 2003
Neurological presentation of Ehlers-Danlos syndrome type IV in a family with parental mosaicismS Palmeri, F Mari, I Meloni, et al.Neuromuscular Disorders : NMD|October 24, 2015
Dropped-head in recessive oculopharyngeal muscular dystrophyMatteo Garibaldi, Elena Maria Pennisi, Mirella Bruttini, et al.Clinical Neuroradiology|December 16, 2017
PTA Stent of Dural Sinuses in Brain DAVF : A Report of 4 CasesLeonardo Renieri, Caterina Michelozzi, Waleed Brinjikji, et al.Cytogenetic and Genome Research|December 11, 2024
The Association between Short Telomere Length and Cardiovascular DiseasePersefoni Fragkiadaki, Miruna-Maria Apetroaei, Elisavet Kouvidi, et al.Genomics|April 16, 1998
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardationM Piccini, F Vitelli, M Bruttini, et al.Pageof 63