Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Laura Obici

Showing results (81-90 of 204) with videos related to

Pageof 21
Sort By:
Journal of the American Society of Nephrology : JASN|October 14, 2005
Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritisGina Gregorini, Claudia Izzi, Laura Obici, et al.
European Journal of Heart Failure|April 29, 2021
Expert consensus on the monitoring of transthyretin amyloid cardiomyopathyPablo Garcia-Pavia, Frank Bengel, Dulce Brito, et al.
JACC. Heart Failure|July 15, 2019
Screening for Transthyretin Amyloid Cardiomyopathy in Everyday PracticeRonald M Witteles, Sabahat Bokhari, Thibaud Damy, et al.
Annals of the Rheumatic Diseases|July 31, 2016
Canakinumab reverses overexpression of inflammatory response genes in tumour necrosis factor receptor-associated periodic syndromeRebecca Torene, Nanguneri Nirmala, Laura Obici, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|July 16, 2025
Role of extracellular space and matrix remodeling in cardiac amyloidosisFrancesca Lavatelli, Loredana Marchese, Palma Patrizia Mangione, et al.
Circulation|April 30, 2003
Serum N-terminal pro-brain natriuretic peptide is a sensitive marker of myocardial dysfunction in AL amyloidosisGiovanni Palladini, Carlo Campana, Catherine Klersy, et al.
Human Mutation|July 22, 2014
Online registry for mutations in hereditary amyloidosis including nomenclature recommendationsDorota M Rowczenio, Islam Noor, Julian D Gillmore, et al.
Seminars in Arthritis and Rheumatism|January 8, 2014
The expanding spectrum of low-penetrance TNFRSF1A gene variants in adults presenting with recurrent inflammatory attacks: clinical manifestations and long-term follow-upLuca Cantarini, Donato Rigante, Giampaolo Merlini, et al.
European Journal of Neurology|April 23, 2025
Quantitative MRI Assessment Using Variable Echo Time Imaging of Peripheral Nerve Injury in ATTRv Amyloidosis PatientsCarlo Asteggiano, Matteo Paoletti, Elisa Vegezzi, et al.
Blood|January 26, 2006
Circulating amyloidogenic free light chains and serum N-terminal natriuretic peptide type B decrease simultaneously in association with improvement of survival in ALGiovanni Palladini, Francesca Lavatelli, Paola Russo, et al.
Pageof 21

Showing results (81-90 of 204) with videos related to

Sort By:
Pageof 21
Journal of the American Society of Nephrology : JASN|October 14, 2005
Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritisGina Gregorini, Claudia Izzi, Laura Obici, et al.
European Journal of Heart Failure|April 29, 2021
Expert consensus on the monitoring of transthyretin amyloid cardiomyopathyPablo Garcia-Pavia, Frank Bengel, Dulce Brito, et al.
JACC. Heart Failure|July 15, 2019
Screening for Transthyretin Amyloid Cardiomyopathy in Everyday PracticeRonald M Witteles, Sabahat Bokhari, Thibaud Damy, et al.
Annals of the Rheumatic Diseases|July 31, 2016
Canakinumab reverses overexpression of inflammatory response genes in tumour necrosis factor receptor-associated periodic syndromeRebecca Torene, Nanguneri Nirmala, Laura Obici, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|July 16, 2025
Role of extracellular space and matrix remodeling in cardiac amyloidosisFrancesca Lavatelli, Loredana Marchese, Palma Patrizia Mangione, et al.
Circulation|April 30, 2003
Serum N-terminal pro-brain natriuretic peptide is a sensitive marker of myocardial dysfunction in AL amyloidosisGiovanni Palladini, Carlo Campana, Catherine Klersy, et al.
Human Mutation|July 22, 2014
Online registry for mutations in hereditary amyloidosis including nomenclature recommendationsDorota M Rowczenio, Islam Noor, Julian D Gillmore, et al.
Seminars in Arthritis and Rheumatism|January 8, 2014
The expanding spectrum of low-penetrance TNFRSF1A gene variants in adults presenting with recurrent inflammatory attacks: clinical manifestations and long-term follow-upLuca Cantarini, Donato Rigante, Giampaolo Merlini, et al.
European Journal of Neurology|April 23, 2025
Quantitative MRI Assessment Using Variable Echo Time Imaging of Peripheral Nerve Injury in ATTRv Amyloidosis PatientsCarlo Asteggiano, Matteo Paoletti, Elisa Vegezzi, et al.
Blood|January 26, 2006
Circulating amyloidogenic free light chains and serum N-terminal natriuretic peptide type B decrease simultaneously in association with improvement of survival in ALGiovanni Palladini, Francesca Lavatelli, Paola Russo, et al.
Pageof 21