Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Elyse Redder"'
Autor:
Elyse Redder, Qiuhong Zhao, Naresh Bumma, Rami Kahwash, Ajay Vallakati, Courtney Campbell, Samir Parikh, Salem Almaani, Miriam Freimer, Yvonne Efebera, Nidhi Sharma
Publikováno v:
Hemato, Vol 3, Iss 3, Pp 414-421 (2022)
Amyloidosis is a rare, systemic disease that can result in significant functional impairment. Specific guidelines for the rehabilitation assessment of amyloidosis patients have yet to be established. The purpose of this study was to identify function
Externí odkaz:
https://doaj.org/article/3db08d15113742039563e3b2e978dc18
Autor:
Naresh Bumma, Rami Kahwash, Samir V. Parikh, Michael Isfort, Miriam Freimer, Ajay Vallakati, Elyse Redder, Courtney M. Campbell, Nidhi Sharma, Yvonne Efebera, Amro Stino
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Amyloidosis refers to a group of conditions where abnormal protein—or amyloid—deposits in tissues or organs, often leading to organ malfunction. Amyloidosis affects nearly any organ system, but especially the heart, kidneys, liver, peripheral ner
Externí odkaz:
https://doaj.org/article/79dd49e6e17c4831b3596097e4d64796
Autor:
Stuart Ramsell, Carlos Arias Bermudez, Cyril Ayuk Mbeng Takem Baiyee, Brandon Rodgers, Samir Parikh, Salem Almaani, Nidhi Sharma, Samantha LoRusso, Miriam Freimer, Elyse Redder, Naresh Bumma, Ajay Vallkati, Yvonne Efebera, Rami Kahwash, Courtney M. Campbell
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
Background:Beta-adrenergic antagonists or blockers (BB) are a cornerstone of cardiac therapy for multiple indications. However, BB are considered relatively contraindicated in amyloid cardiomyopathy due to poor tolerance. This intolerance is hypothes
Externí odkaz:
https://doaj.org/article/a54d0208aa944f7da9e7bc1557216c9d
Autor:
Michael Ozga, Qiuhong Zhao, Don Benson Jr., Patrick Elder, Nita Williams, Naresh Bumma, Ashley Rosko, Maria Chaudhry, Abdullah Khan, Srinivas Devarakonda, Rami Kahwash, Ajay Vallakati, Courtney Campbell, Samir V. Parikh, Salem Almaani, Jason Prosek, Jordan Bittengle, Katherine Pfund, Samantha LoRusso, Miriam Freimer, Elyse Redder, Yvonne Efebera, Nidhi Sharma
Publikováno v:
Cancer Medicine, Vol 10, Iss 3, Pp 965-973 (2021)
Abstract Background Systemic light chain (AL) amyloidosis is a clonal plasma‐cell neoplasm that carries a poor prognosis. Although AL amyloidosis and Multiple Myeloma (MM) can co‐exist and share various cytogenetic chromosomal abnormalities, litt
Externí odkaz:
https://doaj.org/article/838fc5affe834c6d83e8b15aaa975cc8
Autor:
Samantha LoRusso, Qiuhong Zhao, Jason Prosek, Katherine Pfund, Srinivas Devarakonda, Ashley E. Rosko, Patrick Elder, Elyse Redder, Ajay Vallakati, Jordan Bittengle, Yvonne A. Efebera, Courtney M. Campbell, Maria Chaudhry, Salem Almaani, Nidhi Sharma, Samir V. Parikh, Naresh Bumma, Don M. Benson, Abdullah Khan, Rami Kahwash, Nita Williams, Miriam Freimer, Michael Ozga
Publikováno v:
Cancer Medicine
Cancer Medicine, Vol 10, Iss 3, Pp 965-973 (2021)
Cancer Medicine, Vol 10, Iss 3, Pp 965-973 (2021)
Background Systemic light chain (AL) amyloidosis is a clonal plasma‐cell neoplasm that carries a poor prognosis. Although AL amyloidosis and Multiple Myeloma (MM) can co‐exist and share various cytogenetic chromosomal abnormalities, little is kno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52a708880211d48cb697907f21da4ca2
http://europepmc.org/articles/PMC7897960
http://europepmc.org/articles/PMC7897960
Publikováno v:
Journal of the National Comprehensive Cancer Network. 18:QIM20-133
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1dcecf81d4bdb33251d0bf09ba9fe8a5
https://doi.org/10.6004/jnccn.2019.7454
https://doi.org/10.6004/jnccn.2019.7454
Autor:
Courtney M. Campbell, Cyril Ayuk Mbeng Takem Baiyee, Salem Almaani, Naresh Bumma, Nidhi Sharma, Samantha LoRusso, Elyse Redder, Jordan Bittengle, Katherine Pfund, Miriam Friemer, Matthew Tong, Rami Kahwash, Yvonne Efebera, Samir Parikh, Ajay Vallakati
Publikováno v:
American Journal of Therapeutics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24fb4a06fc1cd9da5ec97b697535d5ee
https://doi.org/10.1097/mjt.0000000000001296
https://doi.org/10.1097/mjt.0000000000001296
Autor:
Miriam Freimer, Elyse Redder, Samantha LoRusso, Nidhi Sharma, Samir M. Parikh, Salem Almaani, Victoria Kalinoski-Dubose, Ajay Vallakati, Courtney M. Campbell, Naresh Bumma, Rami Kahwash, Yvonne A. Efebera
Publikováno v:
Circulation. 142
Introduction: Hereditary transthyretin amyloidosis (ATTR) is an autosomal dominant disease, in which destabilized transthyretin protein misfolds and deposits in tissue leading to organ dysfunction. The most common mutation in the United States, trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09705138857df287c726330a1af17eb1
https://doi.org/10.1161/circ.142.suppl_3.17058
https://doi.org/10.1161/circ.142.suppl_3.17058
Autor:
Sarah A Wall, Elyse Redder, Edmund Folefac, Carolyn J Presley, Brittany Knauss, Amy Compston, Ashley E. Rosko
Publikováno v:
Journal of Geriatric Oncology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2291149be54eb01eaf317b5f487b4e80
Autor:
Nita Williams, Srinivas Devarakonda, Qiuhong Zhao, Ashley E. Rosko, Don M. Benson, Nidhi Sharma, Ajay Vallakati, Yvonne A. Efebera, Salem Almaani, Samir M. Parikh, Naresh Bumma, Michael Ozga, Abdullah Khan, Rami Kahwash, Jason Prosek, Patrick Elder, Courtney M. Campbell, Elyse Redder, Maria Chaudhry
Publikováno v:
Biology of Blood and Marrow Transplantation. 26:S229-S230
Introduction Autologous stem cell transplantation (ASCT) remains an effective treatment option for many patients with systemic AL amyloidosis (AL). However, the decision to utilize maintenance therapy following ASCT remains controversial and largely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d69ae9f6ffa85424d092eef1434841d
https://doi.org/10.1016/j.bbmt.2019.12.470
https://doi.org/10.1016/j.bbmt.2019.12.470