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American Journal of Clinical Pathology|March 4, 2005
Performance of an automated immature granulocyte count as a predictor of neonatal sepsisKelly G Nigro, MaryAnn O'Riordan, Eleanor J Molloy, et al.European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|February 26, 2013
Endograft repair of complicated acute type B aortic dissectionsJ Sobocinski, N V Dias, L Berger, et al.Prenatal Diagnosis|June 9, 1999
Low levels of natural killer cells in pregnant women transmitting Toxoplasma gondiiG Nigro, J Piazze, R Paesano, et al.Mitochondrial DNA. Part B, Resources|June 28, 2021
The complete mitochondrial genome of the chocolate chip sea cucumber <i>Isostichopus badionotus</i> (Echinodermata: Holothuroidea)Victoria I Drake, Erica Kim, Hailee G Nigro, et al.Acta Paediatrica (Oslo, Norway : 1992)|October 1, 1992
Chlamydia trachomatis in neonatal respiratory distress of very preterm babies: biphasic clinical pictureD Sollecito, M Midulla, M Bavastrelli, et al.European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|February 7, 2012
Technical note and results in the management of anatomical variants of renal vascularisation during endovascular aneurysm repairR Spear, B Maurel, J Sobocinski, et al.European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|July 22, 2014
Impact of hybrid rooms with image fusion on radiation exposure during endovascular aortic repairA Hertault, B Maurel, J Sobocinski, et al.Journal of Travel Medicine|October 17, 1998
Sexually active adolescents and young adults: a high-risk group for Chlamydia trachomatis infectionM Bavastrelli, M Midulla, D Rossi, et al.Archives of Virology|January 1, 1997
Mother to infant transmission of coinfection by human immunodeficiency virus and hepatitis C virus: prevalence and clinical manifestationsG Nigro, F D'Orio, S Catania, et al.Human Molecular Genetics|October 1, 1992
Detection of a nonsense mutation in the dystrophin gene by multiple SSCPV Nigro, L Politano, G Nigro, et al.Pageof 14