Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Kemi Olugemo"'
Autor:
Thomas H. Brannagan, Michaela Auer-Grumbach, John L. Berk, Chiara Briani, Vera Bril, Teresa Coelho, Thibaud Damy, Angela Dispenzieri, Brian M. Drachman, Nowell Fine, Hanna K. Gaggin, Morie Gertz, Julian D. Gillmore, Esther Gonzalez, Mazen Hanna, David R. Hurwitz, Sami L. Khella, Mathew S. Maurer, Jose Nativi-Nicolau, Kemi Olugemo, Luis F. Quintana, Andrew M. Rosen, Hartmut H. Schmidt, Jacqueline Shehata, Marcia Waddington-Cruz, Carol Whelan, Frederick L. Ruberg
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-13 (2021)
Abstract Background The global spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection causing the ongoing coronavirus disease 2019 (COVID-19) pandemic has raised serious concern for patients with chronic disease. A correlati
Externí odkaz:
https://doaj.org/article/b9e4c37d2b9b46ff846198a89fb03767
Autor:
Michaela Auer-Grumbach, Esther Gonzalez, Brian M. Drachman, Chiara Briani, Andrew M. Rosen, Morie A. Gertz, Angela Dispenzieri, Frederick L. Ruberg, Márcia Waddington-Cruz, Julian D. Gillmore, David R. Hurwitz, Thomas H. Brannagan, Hanna K. Gaggin, Hartmut Schmidt, Luis F. Quintana, Kemi Olugemo, Thibaud Damy, Teresa Coelho, John L. Berk, Vera Bril, Jacqueline Shehata, Mazen Hanna, Nowell M. Fine, Carol J. Whelan, Jose Nativi-Nicolau, Sami Khella, Mathew S. Maurer
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-13 (2021)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
BackgroundThe global spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection causing the ongoing coronavirus disease 2019 (COVID-19) pandemic has raised serious concern for patients with chronic disease. A correlation has bee
Publikováno v:
Public Health – Open Journal. 5:38-41
Publikováno v:
Heart & Lung. 50:564-565
Background Hereditary transthyretin amyloidosis (hATTR or ATTRv [variant]) is a progressive and fatal disease caused by mutations in the transthyretin gene (TTR) that result in the deposition of misfolded TTR protein in major organs and systems, lead
Autor:
Anna Mazzeo, Carol J. Whelan, Morie A. Gertz, John L. Berk, Violaine Planté-Bordeneuve, Isabel Conceição, Brian M. Drachman, Hartmut Schmidt, Peter D. Gorevic, Merrill D. Benson, Arnt V. Kristen, Josep Maria Campistol Plana, Michael Polydefkis, Teresa Coelho, Giampaolo Merlini, Josep Gamez, Annabel K. Wang, Peter J. Dyck, Thomas H. Brannagan, Peter Aquino, Arvind Narayana, Laura Obici, Kemi Olugemo
Publikováno v:
Journal of the Neurological Sciences. 429:117867
Autor:
Jill S. Dolinsky, Catherine N. Marti, Ajay Vallakati, Aaron Gabriel, Arvind Narayana, Andrew M. Keller, Kemi Olugemo, Diego H. Delgado, Keyur B. Shah, Olakunle O. Akinboboye
Publikováno v:
Heart & Lung. 50:564
Background Hereditary transthyretin amyloidosis (hATTR or ATTRv [variant]) is a progressive, and fatal disease caused by mutations in the transthyretin (TTR) gene. These mutations destabilize protein folding, resulting in amyloid deposits and causing
Autor:
Arvind Narayana, Naresh Bumma, Aaron Gabriel, Kemi Olugemo, Sami Khella, Andrew M. Keller, Keyur B. Shah, Diego H. Delgado
Publikováno v:
Journal of the American College of Cardiology. 77:742
Autor:
Jill S. Dolinsky, Catherine N. Marti, Kemi Olugemo, Keyur B. Shah, Olakunle O. Akinboboye, Arvind Narayana, Diego H. Delgado, Andrew M. Keller, Aaron Gabriel, Ajay Vallakati
Publikováno v:
Journal of the American College of Cardiology. 77:888
Autor:
Diego H. Delgado, Keyur B. Shah, Olakunle O. Akinboboye, Andrew M. Keller, Ajay Vallakati, Catherine N. Marti, Kemi Olugemo, Arvind Narayana, Aaron Gabriel, Jill Dolinsky
Publikováno v:
Journal of Cardiac Failure. 26:S84-S85
Introduction Hereditary transthyretin amyloidosis (hATTR/ATTRv) is a progressive, and fatal disease caused by mutations in the transthyretin gene (TTR). These mutations destabilize protein folding, resulting in amyloid deposits and causing multisyste
Autor:
Chafic Karam, Sami Khella, Aaron Gabriel, Naresh Bumma, Kemi Olugemo, Diego H. Delgado, Andrew M. Keller, Keyur B. Shah, Arvind Narayana
Publikováno v:
Journal of Cardiac Failure. 26:S84
Introduction Heart failure due to cardiomyopathy is a frequent manifestation of hereditary transthyretin amyloidosis (hATTR), a progressive, multisystem, and fatal disease that results from the deposition of misfolded transthyretin (TTR) protein in m