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E Savin

Showing results (21-30 of 32) with videos related to

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Journal of the European Academy of Dermatology and Venereology : JEADV|April 8, 2020
Poor prognosis of drug-induced and acute graft-versus-host disease-induced epidermal necrolysis in bone marrow/stem cell transplant recipients: a retrospective case seriesS F Roy, F M Ghazawi, A Alsarheed, et al.
The European Journal of Medicine|April 1, 1993
Relationship between birth weight and umbilical Doppler blood flow velocity waveforms during the third trimester of pregnancyP Bonnin, O Bailliart, W Kedra, et al.
Current Oncology (Toronto, Ont.)|July 17, 2020
Investigating epidemiologic trends and the geographic distribution of patients with anal squamous cell carcinoma throughout CanadaL Cattelan, F M Ghazawi, M Le, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|January 1, 1990
Peritonitis-related deaths in continuous ambulatory peritoneal dialysis (CAPD) patientsG E Digenis, G Abraham, E Savin, et al.
Journal of Perinatal Medicine|January 1, 1997
Evidence of fetal cerebral vasodilatation induced by submaximal maternal dynamic exercise in human pregnancyP Bonnin, C Bazzi-Grossin, N Ciraru-Vigneron, et al.
Prenatal Diagnosis|May 1, 1985
Cystic hygroma: prenatal diagnosis and genetic counsellingC Marchese, E Savin, E Dragone, et al.
Current Oncology (Toronto, Ont.)|June 4, 2020
Epidemiology of adult and pediatric Burkitt lymphoma in Canada: sequelae of the HIV epidemicS F Roy, F M Ghazawi, M Le, et al.
Prenatal Diagnosis|August 12, 2004
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal surveyA Sensi, S Cavani, N Villa, et al.
Human Genetics|January 1, 1982
Cytogenetic findings in 4952 prenatal diagnoses. An Italian collaborative studyG Simoni, M Fraccaro, A Arslanian, et al.
Clinical Genetics|March 16, 2017
Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genesE Di Gregorio, E Riberi, E F Belligni, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Journal of the European Academy of Dermatology and Venereology : JEADV|April 8, 2020
Poor prognosis of drug-induced and acute graft-versus-host disease-induced epidermal necrolysis in bone marrow/stem cell transplant recipients: a retrospective case seriesS F Roy, F M Ghazawi, A Alsarheed, et al.
The European Journal of Medicine|April 1, 1993
Relationship between birth weight and umbilical Doppler blood flow velocity waveforms during the third trimester of pregnancyP Bonnin, O Bailliart, W Kedra, et al.
Current Oncology (Toronto, Ont.)|July 17, 2020
Investigating epidemiologic trends and the geographic distribution of patients with anal squamous cell carcinoma throughout CanadaL Cattelan, F M Ghazawi, M Le, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|January 1, 1990
Peritonitis-related deaths in continuous ambulatory peritoneal dialysis (CAPD) patientsG E Digenis, G Abraham, E Savin, et al.
Journal of Perinatal Medicine|January 1, 1997
Evidence of fetal cerebral vasodilatation induced by submaximal maternal dynamic exercise in human pregnancyP Bonnin, C Bazzi-Grossin, N Ciraru-Vigneron, et al.
Prenatal Diagnosis|May 1, 1985
Cystic hygroma: prenatal diagnosis and genetic counsellingC Marchese, E Savin, E Dragone, et al.
Current Oncology (Toronto, Ont.)|June 4, 2020
Epidemiology of adult and pediatric Burkitt lymphoma in Canada: sequelae of the HIV epidemicS F Roy, F M Ghazawi, M Le, et al.
Prenatal Diagnosis|August 12, 2004
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal surveyA Sensi, S Cavani, N Villa, et al.
Human Genetics|January 1, 1982
Cytogenetic findings in 4952 prenatal diagnoses. An Italian collaborative studyG Simoni, M Fraccaro, A Arslanian, et al.
Clinical Genetics|March 16, 2017
Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genesE Di Gregorio, E Riberi, E F Belligni, et al.
Pageof 4