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Per Westermark
Giampaolo Merlini

Showing results (221-230 of 587) with videos related to

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The Journal of Pathology|December 19, 2001
Medin and medin-amyloid in ageing inflamed and non-inflamed temporal arteriesSiwei Peng, Gunilla T Westermark, Jan Näslund, et al.
Upsala Journal of Medical Sciences|February 6, 2016
(99m)Tc-DPD uptake reflects amyloid fibril composition in hereditary transthyretin amyloidosisBjörn Pilebro, Ole B Suhr, Ulf Näslund, et al.
Scientific Reports|March 17, 2026
Cardiac phenotype in hereditary transthyretin amyloidosis: correlations between fibril types and 99mTc-DPD uptakeViktor Löfbacka, Jonas Wixner, Per Westermark, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 12, 2017
Diagnostic challenges in hereditary transthyretin amyloidosis with polyneuropathy: avoiding misdiagnosis of a treatable hereditary neuropathyAndrea Cortese, Elisa Vegezzi, Alessandro Lozza, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|July 14, 2005
Multicentre versus single centre approach to rare diseases: the model of systemic light chain amyloidosisGiovanni Palladini, Robert A Kyle, Dirk R Larson, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 5, 2011
Effect of the amyloidogenic L75P apolipoprotein A-I variant on HDL subpopulationsMonica Gomaraschi, Laura Obici, Sara Simonelli, et al.
American Journal of Hematology|December 22, 2018
High sensitivity M-protein detection in a case of light-chain cardiac amyloidosis without evidence of plasma cell dyscrasiaAbdulrahman M Saadalla, Avinainder Singh, David Barnidge, et al.
Annals of the Rheumatic Diseases|December 22, 2010
Favourable and sustained response to anakinra in tumour necrosis factor receptor-associated periodic syndrome (TRAPS) with or without AA amyloidosisLaura Obici, Antonella Meini, Marco Cattalini, et al.
Blood|July 18, 2018
Monoclonal gammopathy of clinical significance: a novel concept with therapeutic implicationsJean-Paul Fermand, Frank Bridoux, Angela Dispenzieri, et al.
Clinical Chemistry and Laboratory Medicine|December 19, 2015
A patient with AL amyloidosis with negative free light chain resultsPaolo Milani, Veronica Valentini, Giovanni Ferraro, et al.
Pageof 59

Showing results (221-230 of 587) with videos related to

Sort By:
Pageof 59
The Journal of Pathology|December 19, 2001
Medin and medin-amyloid in ageing inflamed and non-inflamed temporal arteriesSiwei Peng, Gunilla T Westermark, Jan Näslund, et al.
Upsala Journal of Medical Sciences|February 6, 2016
(99m)Tc-DPD uptake reflects amyloid fibril composition in hereditary transthyretin amyloidosisBjörn Pilebro, Ole B Suhr, Ulf Näslund, et al.
Scientific Reports|March 17, 2026
Cardiac phenotype in hereditary transthyretin amyloidosis: correlations between fibril types and 99mTc-DPD uptakeViktor Löfbacka, Jonas Wixner, Per Westermark, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 12, 2017
Diagnostic challenges in hereditary transthyretin amyloidosis with polyneuropathy: avoiding misdiagnosis of a treatable hereditary neuropathyAndrea Cortese, Elisa Vegezzi, Alessandro Lozza, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|July 14, 2005
Multicentre versus single centre approach to rare diseases: the model of systemic light chain amyloidosisGiovanni Palladini, Robert A Kyle, Dirk R Larson, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 5, 2011
Effect of the amyloidogenic L75P apolipoprotein A-I variant on HDL subpopulationsMonica Gomaraschi, Laura Obici, Sara Simonelli, et al.
American Journal of Hematology|December 22, 2018
High sensitivity M-protein detection in a case of light-chain cardiac amyloidosis without evidence of plasma cell dyscrasiaAbdulrahman M Saadalla, Avinainder Singh, David Barnidge, et al.
Annals of the Rheumatic Diseases|December 22, 2010
Favourable and sustained response to anakinra in tumour necrosis factor receptor-associated periodic syndrome (TRAPS) with or without AA amyloidosisLaura Obici, Antonella Meini, Marco Cattalini, et al.
Blood|July 18, 2018
Monoclonal gammopathy of clinical significance: a novel concept with therapeutic implicationsJean-Paul Fermand, Frank Bridoux, Angela Dispenzieri, et al.
Clinical Chemistry and Laboratory Medicine|December 19, 2015
A patient with AL amyloidosis with negative free light chain resultsPaolo Milani, Veronica Valentini, Giovanni Ferraro, et al.
Pageof 59