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A Corsini

Showing results (141-150 of 157) with videos related to

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Journal of Orthopaedics and Traumatology : Official Journal of the Italian Society of Orthopaedics and Traumatology|September 19, 2017
Cam morphology and inguinal pathologies: is there a possible connection?G N Bisciotti, F Di Marzo, A Auci, et al.
Gut|April 6, 1999
Analysis of Helicobacter pylori vacA and cagA genotypes and serum antibody profile in benign and malignant gastroduodenal diseasesD Basso, F Navaglia, L Brigato, et al.
Atherosclerosis|December 1, 2009
Increased atherosclerosis and vascular inflammation in APP transgenic mice with apolipoprotein E deficiencyG Tibolla, G D Norata, C Meda, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 1, 1997
Pharmacological control of the mevalonate pathway: effect on arterial smooth muscle cell proliferationM Raiteri, L Arnaboldi, P McGeady, et al.
Environment International|February 8, 2021
Maternal exposure to air pollutants, PCSK9 levels, fetal growth and gestational age - An Italian cohortC Macchi, S Iodice, N Persico, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|July 1, 1997
[Follow-up of residual renal function in patients with serious forms of posterior urethral valves]V A Mei, A Corsini, F P Di Lorenzo, et al.
Parasitology Research|September 25, 2021
Dot blot platform as a novel diagnostic kit: rapid, accurate, and on-site detection of Schistosoma mansoni in urine samples of hard to detect individualsMaria Luysa C Pedrosa, Alana K de Oliveira, Caroline Pereira, et al.
Cardiovascular Diabetology|November 4, 2020
Depression and cardiovascular risk-association among Beck Depression Inventory, PCSK9 levels and insulin resistanceC Macchi, C Favero, A Ceresa, et al.
Atherosclerosis|January 22, 2003
Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH geneC M Barbagallo, G Emmanuele, A B Cefalù, et al.
Clinical and Experimental Medicine|February 9, 2002
Italian familial defective apolipoprotein B patients share a unique haplotype with other Caucasian patientsA B Cefalù, C M Barbagallo, E Sesti, et al.
Pageof 16

Showing results (141-150 of 157) with videos related to

Sort By:
Pageof 16
Journal of Orthopaedics and Traumatology : Official Journal of the Italian Society of Orthopaedics and Traumatology|September 19, 2017
Cam morphology and inguinal pathologies: is there a possible connection?G N Bisciotti, F Di Marzo, A Auci, et al.
Gut|April 6, 1999
Analysis of Helicobacter pylori vacA and cagA genotypes and serum antibody profile in benign and malignant gastroduodenal diseasesD Basso, F Navaglia, L Brigato, et al.
Atherosclerosis|December 1, 2009
Increased atherosclerosis and vascular inflammation in APP transgenic mice with apolipoprotein E deficiencyG Tibolla, G D Norata, C Meda, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 1, 1997
Pharmacological control of the mevalonate pathway: effect on arterial smooth muscle cell proliferationM Raiteri, L Arnaboldi, P McGeady, et al.
Environment International|February 8, 2021
Maternal exposure to air pollutants, PCSK9 levels, fetal growth and gestational age - An Italian cohortC Macchi, S Iodice, N Persico, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|July 1, 1997
[Follow-up of residual renal function in patients with serious forms of posterior urethral valves]V A Mei, A Corsini, F P Di Lorenzo, et al.
Parasitology Research|September 25, 2021
Dot blot platform as a novel diagnostic kit: rapid, accurate, and on-site detection of Schistosoma mansoni in urine samples of hard to detect individualsMaria Luysa C Pedrosa, Alana K de Oliveira, Caroline Pereira, et al.
Cardiovascular Diabetology|November 4, 2020
Depression and cardiovascular risk-association among Beck Depression Inventory, PCSK9 levels and insulin resistanceC Macchi, C Favero, A Ceresa, et al.
Atherosclerosis|January 22, 2003
Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH geneC M Barbagallo, G Emmanuele, A B Cefalù, et al.
Clinical and Experimental Medicine|February 9, 2002
Italian familial defective apolipoprotein B patients share a unique haplotype with other Caucasian patientsA B Cefalù, C M Barbagallo, E Sesti, et al.
Pageof 16