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L Papi

Showing results (31-40 of 46) with videos related to

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Coronary Artery Disease|January 1, 1993
Evidence for a systemic defect of resistance-sized arterioles in hypertrophic cardiomyopathyR Pedrinelli, M Spessot, G Chiriatti, et al.
Human Molecular Genetics|January 1, 1994
The neurofibromatosis type 2 gene is inactivated in schwannomasE C Twist, M H Ruttledge, M Rousseau, et al.
Clinical Genetics|February 1, 2005
A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancerE Lucci-Cordisco, M Zollino, S Baglioni, et al.
Giornale Italiano Di Cardiologia|June 1, 1991
[Myocardial scintigraphy with 99mTc MIBI. The use of a single-day protocol in a multiregional center: a comparison between planar and tomographic imaging]G Marcucci, R Sciagrà, N R Petix, et al.
European Journal of Clinical Pharmacology|January 1, 1987
Plasma renin activity does not predict the antihypertensive efficacy of chlorthalidoneA Salvetti, R Pedrinelli, G Bartolomei, et al.
Journal of the American College of Cardiology|March 15, 1991
Coronary vasodilation is impaired in both hypertrophied and nonhypertrophied myocardium of patients with hypertrophic cardiomyopathy: a study with nitrogen-13 ammonia and positron emission tomographyP Camici, G Chiriatti, R Lorenzoni, et al.
Giornale Italiano Di Cardiologia|July 1, 1991
[Regional myocardial perfusion and ischemia in hypertrophic cardiomyopathy]G Chiriatti, L Papi, R Gistri, et al.
Annals of Human Genetics|May 31, 2007
Fatal malonyl CoA decarboxylase deficiency due to maternal uniparental isodisomy of the telomeric end of chromosome 16S Malvagia, L Papi, A Morrone, et al.
Clinical Genetics|June 29, 2017
A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiencyI Paganini, R Sestini, G L Capone, et al.
Nucleic Acids Research|March 25, 1993
Duplicated KOX zinc finger gene clusters flank the centromere of human chromosome 10: evidence for a pericentric inversion during primate evolutionA Tunnacliffe, L Liu, J K Moore, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Coronary Artery Disease|January 1, 1993
Evidence for a systemic defect of resistance-sized arterioles in hypertrophic cardiomyopathyR Pedrinelli, M Spessot, G Chiriatti, et al.
Human Molecular Genetics|January 1, 1994
The neurofibromatosis type 2 gene is inactivated in schwannomasE C Twist, M H Ruttledge, M Rousseau, et al.
Clinical Genetics|February 1, 2005
A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancerE Lucci-Cordisco, M Zollino, S Baglioni, et al.
Giornale Italiano Di Cardiologia|June 1, 1991
[Myocardial scintigraphy with 99mTc MIBI. The use of a single-day protocol in a multiregional center: a comparison between planar and tomographic imaging]G Marcucci, R Sciagrà, N R Petix, et al.
European Journal of Clinical Pharmacology|January 1, 1987
Plasma renin activity does not predict the antihypertensive efficacy of chlorthalidoneA Salvetti, R Pedrinelli, G Bartolomei, et al.
Journal of the American College of Cardiology|March 15, 1991
Coronary vasodilation is impaired in both hypertrophied and nonhypertrophied myocardium of patients with hypertrophic cardiomyopathy: a study with nitrogen-13 ammonia and positron emission tomographyP Camici, G Chiriatti, R Lorenzoni, et al.
Giornale Italiano Di Cardiologia|July 1, 1991
[Regional myocardial perfusion and ischemia in hypertrophic cardiomyopathy]G Chiriatti, L Papi, R Gistri, et al.
Annals of Human Genetics|May 31, 2007
Fatal malonyl CoA decarboxylase deficiency due to maternal uniparental isodisomy of the telomeric end of chromosome 16S Malvagia, L Papi, A Morrone, et al.
Clinical Genetics|June 29, 2017
A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiencyI Paganini, R Sestini, G L Capone, et al.
Nucleic Acids Research|March 25, 1993
Duplicated KOX zinc finger gene clusters flank the centromere of human chromosome 10: evidence for a pericentric inversion during primate evolutionA Tunnacliffe, L Liu, J K Moore, et al.
Pageof 5