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P Gasparini

Showing results (51-60 of 204) with videos related to

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Human Mutation|March 29, 2000
Detection of two novel large deletions in SLC3A1 by semi-quantitative fluorescent multiplex PCRJ Purroy, L Bisceglia, J Jaeken, et al.
Journal of Medical Genetics|August 27, 1998
Usher syndrome type III (USH3) linked to chromosome 3q in an Italian familyP Gasparini, A De Fazio, A I Croce, et al.
Recenti Progressi in Medicina|March 1, 1994
[Immune hemolytic anemia and acute kidney failure due to rifampicin]F Guzzini, F Angiolini, L Cazzaniga, et al.
Journal of Internal Medicine|March 1, 1992
Prevalence of hyperinsulinaemia in patients with high blood pressureI Zavaroni, S Mazza, E Dall'Aglio, et al.
American Journal of Medical Genetics. Part A|January 8, 2005
A novel GJA1 mutation causes oculodentodigital dysplasia without syndactylyC Vitiello, P D'Adamo, F Gentile, et al.
The American Journal of Cardiology|May 1, 1994
Cigarette smokers are relatively glucose intolerant, hyperinsulinemic and dyslipidemicI Zavaroni, L Bonini, P Gasparini, et al.
Bone Marrow Transplantation|December 1, 1989
Bone marrow transplantation monitoring by DNA analysisP Gasparini, G Martinelli, E Trabetti, et al.
The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
Can weight gain in healthy, nonobese volunteers be predicted by differences in baseline plasma insulin concentration?I Zavaroni, A Zuccarelli, P Gasparini, et al.
Human Genetics|September 1, 1990
Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF familiesG Novelli, P Gasparini, A Savoia, et al.
European Journal of Pediatrics|December 1, 1993
Cystic fibrosis: the delta F508 mutation does not lead to an exceptionally severe phenotype. A cohort studyG Borgo, P Gasparini, A Bonizzato, et al.
Pageof 21

Showing results (51-60 of 204) with videos related to

Sort By:
Pageof 21
Human Mutation|March 29, 2000
Detection of two novel large deletions in SLC3A1 by semi-quantitative fluorescent multiplex PCRJ Purroy, L Bisceglia, J Jaeken, et al.
Journal of Medical Genetics|August 27, 1998
Usher syndrome type III (USH3) linked to chromosome 3q in an Italian familyP Gasparini, A De Fazio, A I Croce, et al.
Recenti Progressi in Medicina|March 1, 1994
[Immune hemolytic anemia and acute kidney failure due to rifampicin]F Guzzini, F Angiolini, L Cazzaniga, et al.
Journal of Internal Medicine|March 1, 1992
Prevalence of hyperinsulinaemia in patients with high blood pressureI Zavaroni, S Mazza, E Dall'Aglio, et al.
American Journal of Medical Genetics. Part A|January 8, 2005
A novel GJA1 mutation causes oculodentodigital dysplasia without syndactylyC Vitiello, P D'Adamo, F Gentile, et al.
The American Journal of Cardiology|May 1, 1994
Cigarette smokers are relatively glucose intolerant, hyperinsulinemic and dyslipidemicI Zavaroni, L Bonini, P Gasparini, et al.
Bone Marrow Transplantation|December 1, 1989
Bone marrow transplantation monitoring by DNA analysisP Gasparini, G Martinelli, E Trabetti, et al.
The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
Can weight gain in healthy, nonobese volunteers be predicted by differences in baseline plasma insulin concentration?I Zavaroni, A Zuccarelli, P Gasparini, et al.
Human Genetics|September 1, 1990
Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF familiesG Novelli, P Gasparini, A Savoia, et al.
European Journal of Pediatrics|December 1, 1993
Cystic fibrosis: the delta F508 mutation does not lead to an exceptionally severe phenotype. A cohort studyG Borgo, P Gasparini, A Bonizzato, et al.
Pageof 21