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S Maffei

Showing results (91-100 of 102) with videos related to

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Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|October 28, 2006
[Substitutive therapies in sepsis and acute renale failure]F Mariano, Z Hollò, D Damiani, et al.
Circulation|May 1, 1993
Effect of medical and surgical therapy on aortic dissection evaluated by transesophageal echocardiography. Implications for prognosis and therapy. The European Cooperative Study Group on EchocardiographyR Erbel, H Oelert, J Meyer, et al.
Cytokine|April 28, 2015
TNFα antagonization alters NOS2 dependent nasopharyngeal carcinoma tumor growthMehdi Bourouba, Ahmed-Amine Zergoun, Joseph S Maffei, et al.
Minerva Urologica E Nefrologica = the Italian Journal of Urology and Nephrology|March 1, 1994
[The value of albumin and cholesterol blood levels as indicators of the risk of death in dialysis. Working Group of the Piedmont Registry of Dialysis and Transplantation]M Salomone, G B Piccoli, F Bonello, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|August 10, 2021
Efficacy of mechanical thrombectomy in patients with ischemic stroke and cancerL Ciolli, G Bigliardi, D Ferraro, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|August 27, 2002
[Costs of dialysis in hospitalised patients with acute or chronic renal failure, according to area of treatment]A Jeantet, G B Piccoli, A Pacitti, et al.
Clinical and Experimental Obstetrics & Gynecology|January 13, 2016
Soy isoflavones, inulin, calcium, and vitamin D3 in post-menopausal hot flushes: an observational studyA Cianci, N Colacurci, A M Paoletti, et al.
Disease Markers|May 3, 2007
A mononucleotide markers panel to identify hMLH1/hMSH2 germline mutationsM Pedroni, B Roncari, S Maffei, et al.
Clinical Genetics|October 7, 2005
Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutationsG Ponti, M Ponz de Leon, S Maffei, et al.
Clinical Genetics|August 28, 2007
Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCCB Roncari, M Pedroni, S Maffei, et al.
Pageof 11

Showing results (91-100 of 102) with videos related to

Sort By:
Pageof 11
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|October 28, 2006
[Substitutive therapies in sepsis and acute renale failure]F Mariano, Z Hollò, D Damiani, et al.
Circulation|May 1, 1993
Effect of medical and surgical therapy on aortic dissection evaluated by transesophageal echocardiography. Implications for prognosis and therapy. The European Cooperative Study Group on EchocardiographyR Erbel, H Oelert, J Meyer, et al.
Cytokine|April 28, 2015
TNFα antagonization alters NOS2 dependent nasopharyngeal carcinoma tumor growthMehdi Bourouba, Ahmed-Amine Zergoun, Joseph S Maffei, et al.
Minerva Urologica E Nefrologica = the Italian Journal of Urology and Nephrology|March 1, 1994
[The value of albumin and cholesterol blood levels as indicators of the risk of death in dialysis. Working Group of the Piedmont Registry of Dialysis and Transplantation]M Salomone, G B Piccoli, F Bonello, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|August 10, 2021
Efficacy of mechanical thrombectomy in patients with ischemic stroke and cancerL Ciolli, G Bigliardi, D Ferraro, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|August 27, 2002
[Costs of dialysis in hospitalised patients with acute or chronic renal failure, according to area of treatment]A Jeantet, G B Piccoli, A Pacitti, et al.
Clinical and Experimental Obstetrics & Gynecology|January 13, 2016
Soy isoflavones, inulin, calcium, and vitamin D3 in post-menopausal hot flushes: an observational studyA Cianci, N Colacurci, A M Paoletti, et al.
Disease Markers|May 3, 2007
A mononucleotide markers panel to identify hMLH1/hMSH2 germline mutationsM Pedroni, B Roncari, S Maffei, et al.
Clinical Genetics|October 7, 2005
Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutationsG Ponti, M Ponz de Leon, S Maffei, et al.
Clinical Genetics|August 28, 2007
Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCCB Roncari, M Pedroni, S Maffei, et al.
Pageof 11