Zobrazeno 1 - 10
of 740
pro vyhledávání: '"Patisiran (Onpattro®)"'
Autor:
Ivan Urits, Daniel Swanson, Michael C. Swett, Anjana Patel, Kevin Berardino, Ariunzaya Amgalan, Amnon A. Berger, Hisham Kassem, Alan D. Kaye, Omar Viswanath
Publikováno v:
Neurology and Therapy, Vol 9, Iss 2, Pp 301-315 (2020)
Abstract Hereditary variant transthyretin amyloidosis (ATTRv) is a rare genetic defect that affects about 5000–10,000 people worldwide, causing amyloidosis secondary to misfolding of mutant transthyretin (TTR) protein fibrils. TTR mutations can cau
Externí odkaz:
https://doaj.org/article/d4411de9a7a947deab62328df510341a
Autor:
Urits, Ivan1 (AUTHOR) iurits@bidmc.harvard.edu, Swanson, Daniel2 (AUTHOR), Swett, Michael C.2 (AUTHOR), Patel, Anjana2 (AUTHOR), Berardino, Kevin2 (AUTHOR), Amgalan, Ariunzaya2 (AUTHOR), Berger, Amnon A.1 (AUTHOR), Kassem, Hisham3 (AUTHOR), Kaye, Alan4 (AUTHOR), Viswanath, Omar5,6,7 (AUTHOR)
Publikováno v:
Neurology & Therapy. Dec2020, Vol. 9 Issue 2, p301-315. 15p.
Autor:
Urits I; Department of Anesthesiology, Critical Care, and Pain Medicine, Beth Israel Deaconess Medical Center-Harvard Medical School, Boston, MA, USA. iurits@bidmc.harvard.edu., Swanson D; Georgetown University School of Medicine, Washington, DC, USA., Swett MC; Georgetown University School of Medicine, Washington, DC, USA., Patel A; Georgetown University School of Medicine, Washington, DC, USA., Berardino K; Georgetown University School of Medicine, Washington, DC, USA., Amgalan A; Georgetown University School of Medicine, Washington, DC, USA., Berger AA; Department of Anesthesiology, Critical Care, and Pain Medicine, Beth Israel Deaconess Medical Center-Harvard Medical School, Boston, MA, USA., Kassem H; Department of Anesthesiology, Mount Sinai Medical Center, Miami Beach, FL, USA., Kaye AD; Department of Anesthesiology, Louisiana State University Health Shreveport, Shreveport, LA, USA., Viswanath O; Valley Anesthesiology and Pain Consultants-Envision Physician Services, Phoenix, AZ, USA.; Department of Anesthesiology, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, USA.; Department of Anesthesiology, Creighton University School of Medicine, Omaha, NE, USA.
Publikováno v:
Neurology and therapy [Neurol Ther] 2021 Jun; Vol. 10 (1), pp. 407.
Autor:
Omar Viswanath, Hisham Kassem, Alan D. Kaye, Daniel Swanson, Anjana Patel, Michael C Swett, Ariunzaya Amgalan, Ivan Urits, Amnon A Berger, Kevin Berardino
Publikováno v:
Neurology and Therapy
Neurology and Therapy, Vol 9, Iss 2, Pp 301-315 (2020)
Neurology and Therapy, Vol 9, Iss 2, Pp 301-315 (2020)
Hereditary variant transthyretin amyloidosis (ATTRv) is a rare genetic defect that affects about 5000–10,000 people worldwide, causing amyloidosis secondary to misfolding of mutant transthyretin (TTR) protein fibrils. TTR mutations can cause protei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e61701f432dddc09bce74fff535eaed
http://europepmc.org/articles/PMC7606409
http://europepmc.org/articles/PMC7606409
Autor:
Omar Viswanath, Hisham Kassem, Daniel Swanson, Ariunzaya Amgalan, Alan D. Kaye, Ivan Urits, Amnon A Berger, Kevin Berardino, Anjana Patel, Michael C Swett
Publikováno v:
Neurology and Therapy
Hereditary variant transthyretin amyloidosis (ATTRv) is a rare genetic defect that affects about 5000-10,000 people worldwide, causing amyloidosis secondary to misfolding of mutant transthyretin (TTR) protein fibrils. TTR mutations can cause protein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e24edfa684ae10330602c8058d4eba5
https://doi.org/10.1007/s40120-020-00228-x
https://doi.org/10.1007/s40120-020-00228-x
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