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F Perfetto

Showing results (51-60 of 56) with videos related to

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Scripta Medica|January 6, 2009
CHRONOBIOLOGY OF HIGH BLOOD PRESSUREG Cornélissen, F Halberg, E E Bakken, et al.
Rheumatology (Oxford, England)|August 29, 2006
Circulating levels of Nepsilon-(carboxymethyl)lysine are increased in systemic sclerosisO Kaloudi, G Basta, F Perfetto, et al.
Journal of Internal Medicine|February 22, 2021
Tenosynovial complications identify TTR cardiac amyloidosis among patients with hypertrophic cardiomyopathy phenotypeF Cappelli, M Zampieri, C Fumagalli, et al.
In Vivo (Athens, Greece)|April 28, 1999
Spin-offs from blood pressure and heart rate studies for health care and space researchF Halberg, G Cornélissen, O Schwartzkopff, et al.
Orphanet Journal of Rare Diseases|December 15, 2020
Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensusM Grandis, L Obici, M Luigetti, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|November 9, 2005
Chronomics, neuroendocrine feedsidewards and the recording and consulting of nowcasts--forecasts of geomagneticsR Jozsa, F Halberg, G Cornélissen, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
Scripta Medica|January 6, 2009
CHRONOBIOLOGY OF HIGH BLOOD PRESSUREG Cornélissen, F Halberg, E E Bakken, et al.
Rheumatology (Oxford, England)|August 29, 2006
Circulating levels of Nepsilon-(carboxymethyl)lysine are increased in systemic sclerosisO Kaloudi, G Basta, F Perfetto, et al.
Journal of Internal Medicine|February 22, 2021
Tenosynovial complications identify TTR cardiac amyloidosis among patients with hypertrophic cardiomyopathy phenotypeF Cappelli, M Zampieri, C Fumagalli, et al.
In Vivo (Athens, Greece)|April 28, 1999
Spin-offs from blood pressure and heart rate studies for health care and space researchF Halberg, G Cornélissen, O Schwartzkopff, et al.
Orphanet Journal of Rare Diseases|December 15, 2020
Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensusM Grandis, L Obici, M Luigetti, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|November 9, 2005
Chronomics, neuroendocrine feedsidewards and the recording and consulting of nowcasts--forecasts of geomagneticsR Jozsa, F Halberg, G Cornélissen, et al.
Pageof 6