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C Magnani

Showing results (161-170 of 187) with videos related to

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Mutation Research|March 28, 2006
Polymorphisms in DNA repair genes as risk factors for asbestos-related malignant mesothelioma in a general population studyI Dianzani, L Gibello, A Biava, et al.
Lupus|April 25, 2013
Anti-IFI16 antibodies and their relation to disease characteristics in systemic lupus erythematosusV Caneparo, T Cena, M De Andrea, et al.
La Medicina Del Lavoro|March 20, 2014
[Consensus Conference on Pleural Mesothelioma: response of the authors]C Magnani, D Mirabelli, Bice Fubini, et al.
Pathologica|June 1, 1996
[Audit of histopathology activities at the pathology departments of 7 general hospitals. 2. Response time]A Andrion, A Gaglio, A Langè, et al.
Pathologica|February 1, 1996
[Audit of histopathological activities in the laboratories of 7 general hospitals. 1. Types of resources and quantitative aspects of the workload]A Andrion, E Feyles, A Langè, et al.
Clinical Genetics|November 13, 2014
Insights into genotype-phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein-Taybi syndrome patientsS Spena, D Milani, D Rusconi, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 13, 2017
Three-dimensional assessment of umbilical vein deviation angle for prediction of liver herniation in left-sided congenital diaphragmatic herniaN Volpe, E Mazzone, B Muto, et al.
British Journal of Cancer|July 7, 2000
Multicentric study on malignant pleural mesothelioma and non-occupational exposure to asbestosC Magnani, A Agudo, C A González, et al.
Genetic Counseling (Geneva, Switzerland)|August 6, 2005
MRI and neurological findings in macrocephaly-cutis marmorata telangiectatica congenita syndrome: report of ten cases and review of the literatureL Garavelli, K Leask, C Zanacca, et al.
Clinical Genetics|January 31, 2014
Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 geneG Negri, D Milani, P Colapietro, et al.
Pageof 19

Showing results (161-170 of 187) with videos related to

Sort By:
Pageof 19
Mutation Research|March 28, 2006
Polymorphisms in DNA repair genes as risk factors for asbestos-related malignant mesothelioma in a general population studyI Dianzani, L Gibello, A Biava, et al.
Lupus|April 25, 2013
Anti-IFI16 antibodies and their relation to disease characteristics in systemic lupus erythematosusV Caneparo, T Cena, M De Andrea, et al.
La Medicina Del Lavoro|March 20, 2014
[Consensus Conference on Pleural Mesothelioma: response of the authors]C Magnani, D Mirabelli, Bice Fubini, et al.
Pathologica|June 1, 1996
[Audit of histopathology activities at the pathology departments of 7 general hospitals. 2. Response time]A Andrion, A Gaglio, A Langè, et al.
Pathologica|February 1, 1996
[Audit of histopathological activities in the laboratories of 7 general hospitals. 1. Types of resources and quantitative aspects of the workload]A Andrion, E Feyles, A Langè, et al.
Clinical Genetics|November 13, 2014
Insights into genotype-phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein-Taybi syndrome patientsS Spena, D Milani, D Rusconi, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 13, 2017
Three-dimensional assessment of umbilical vein deviation angle for prediction of liver herniation in left-sided congenital diaphragmatic herniaN Volpe, E Mazzone, B Muto, et al.
British Journal of Cancer|July 7, 2000
Multicentric study on malignant pleural mesothelioma and non-occupational exposure to asbestosC Magnani, A Agudo, C A González, et al.
Genetic Counseling (Geneva, Switzerland)|August 6, 2005
MRI and neurological findings in macrocephaly-cutis marmorata telangiectatica congenita syndrome: report of ten cases and review of the literatureL Garavelli, K Leask, C Zanacca, et al.
Clinical Genetics|January 31, 2014
Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 geneG Negri, D Milani, P Colapietro, et al.
Pageof 19