Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Steve R. Zeldenrust"'
Autor:
Eli Muchtar, Susanne R. Hayman, David Dingli, Morie A. Gertz, Amie Fonder, Shaji Kumar, Steve R. Zeldenrust, Stephen J. Russell, Angela Dispenzieri, Francis K. Buadi, Rahma Warsame, Nelson Leung, Miriam Hobbs, Prashant Kapoor, Taxiarchis Kourelis, Martha Q. Lacy, Ronald S. Go, S. Vincent Rajkumar, Wilson I. Gonsalves, Yi L. Hwa, Robert A. Kyle
Publikováno v:
Leukemia. 33:1268-1272
It is well known that staging of patients with AL amyloidosis at diagnosis predicts for survival, but there is a paucity of literature delineating the prognostic value of these systems at relapse. We evaluated the prognostic value of AL staging among
Autor:
Kyle W. Klarich, Steve R. Zeldenrust, Richard C. Daly, Brooks S. Edwards, Morie A. Gertz, Martha Grogan, Dipti Banerjee, Julie K. Heimbach, Paul L. Swiecicki, John J. Poterucha, Angela Dispenzieri, Lindsey E. Roeker
Publikováno v:
Progress in Transplantation. 27:246-250
Background: Familial transthyretin amyloidosis is a disease caused by misfolded transthyretin aggregates that can impair multiple organ systems. Liver transplantation is the first-line treatment for familial transthyretin amyloidosis. Research Questi
Autor:
Yi L. Hwa, Shaji Kumar, Morie A. Gertz, Francis K. Buadi, Taxiarchis Kourelis, Ronald S. Go, Wilson I. Gonsalves, David Dingli, Prashant Kapoor, Angela Dispenzieri, Susanne R. Hayman, Steve R. Zeldenrust, Miriam Hobbs, Nelson Leung, Amie Fonder, Martha Q. Lacy, Stephen J. Russell, Rahma Warsame, S. Vincent Rajkumar
Publikováno v:
Blood. 130(13)
Among patients with immunoglobulin light chain (AL) amyloidosis, there is little consensus on when reinstitution of chemotherapy should occur. We conducted a retrospective study to evaluate the patterns of relapse or progression (R/P) and the timing
Autor:
Nelson Leung, Shaji Kumar, Steve R. Zeldenrust, Jerry A. Katzmann, Suzanne R. Hayman, Marina Ramirez-Alvarado, Morie A. Gertz, Colin L. Colby, S. Vincent Rajkumar, Martha Q. Lacy, Raynell J. Clark, Francis K. Buadi, Dirk R. Larson, Angela Dispenzieri, Robert A. Kyle
Publikováno v:
Blood. 116:5126-5129
Immunoglobulin free light chains (FLCs) are the precursors of amyloid fibrils in primary amyloidosis (AL). We studied the relationship between FLC levels and clinical features in 730 patients with newly diagnosed AL. The plasma cell clone was λ in 7
Autor:
Vincent Rajkumar, Morie A. Gertz, Martha Grogan, John A. Lust, Giampaolo Merlini, Mathew S. Maurer, Shaji Kumar, Yi Hwa, Robert A. Kyle, Francis K. Baudi, Angela Dispenzieri, Paolo Milani, Martha Q. Lacy, Yi Lin, Ronald S. Go, Nelson Leung, Prashant Kapoor, David Dingli, Suzanne R. Hayman, Kyle W. Klarich, Steve R. Zeldenrust
Publikováno v:
Journal of the American College of Cardiology. 67:1601
Autor:
Morie A. Gertz, Nelson Leung, Steve R. Zeldenrust, S. Vincent Rajkumar, Shaji Kumar, Philip R. Greipp, Colin L. Colby, David Dingli, Martha Q. Lacy, Stephen J. Russell, Suzanne R. Hayman, Kristina Laumann, Angela Dispenzieri, Robert A. Kyle, Francis K. Buadi, John A. Lust
Publikováno v:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 30(9)
Purpose Cardiac involvement predicts poor prognosis in light chain (AL) amyloidosis, and the current prognostic classification is based on cardiac biomarkers troponin-T (cTnT) and N-terminal pro–B-type natriuretic peptide (NT-ProBNP). However, long
Autor:
Robert A. Kyle, Shaji Kumar, Morie A. Gertz, Angela Dispenzieri, Martha Q. Lacy, Francis K. Buadi, S. Vincent Rajkumar, Nelson Leung, Suzanne R. Hayman, Steve R. Zeldenrust
Publikováno v:
Mayo Clinic proceedings. 83(3)
To determine the prognostic value of serum uric acid (UA) in patients with primary systemic (light chain) amyloidosis (AL).A cohort of 1977 patients with newly diagnosed AL seen at our institution between April 1, 1960, and August 1, 2006, and 293 pa
Autor:
Marina Ramirez-Alvarado, Steve R. Zeldenrust, Angela Dispenzieri, Nelson Leung, Batia Kaplan, Gloria Gallo, Avi Livneh
Publikováno v:
Clinical Chemical Laboratory Medicine. 46
Background The presence of monoclonal immunoglobulin free light chains (FLC) in the serum is commonly associated with the gammopathies, including multiple myeloma, systemic light chain amyloidosis and non-amyloid light chain deposition disease. Altho
Autor:
Angela Dispenzieri, Alan H. Bryce, Rafael Fonseca, Rhett P. Ketterling, Shaji Kumar, Suzanne R. Hayman, Martha Q. Lacy, John A. Lust, David Dingli, P R Greipp, Steve R. Zeldenrust, Robert A. Kyle, Vincent Rajkumar, Morie A. Gertz, Francis K. Buadi, Stephen J. Russell
Publikováno v:
Blood. 110:2477-2477
Background: Primary systemic amyloidosis is an uncommon plasma cell dyscrasia characterized by organ deposition of immunoglobulin light or heavy chain fragments. It is related to the other plasma cell dyscrasias such as multiple myeloma and monoclona
Autor:
Robert A. Kyle, Roshini S. Abraham, Raynell J. Clark, Ivana M. Micallef, Steve R. Russell, Morie A. Gertz, Angela Dispenzieri, Suzanne R. Hayman, Shaji Kumar, Philip R. Greipp, David J. Inwards, Michelle A. Elliott, Martha Q. Lacy, S. M. Ansell, Mark R. Litzow, S. Vincent Rajkumar, Patrick B. Johnston, Thomas E. Witzig, John A. Lust, Steve R. Zeldenrust, Jerry A. Katzmann, Luis F. Porrata
Publikováno v:
Blood. 106:422-422
Introduction: The immunoglobulin free light chain (FLC) is the precursor protein of amyloid in primary systemic amyloidosis (AL). Historically, the ability to monitor the amyloid protein precursor has been crude. There is now a test that reproducibly