Web Images Videos Maps News Shopping Gmail more »
Sign in
Scholar Home  
  Advanced Scholar Search
Scholar Preferences
Scholar Results 1 - 10 of about 68 citing Dember: Effect of dose-intensive intravenous melphalan and autologous blood stem-cell transplanta.... (0.10 sec) 

Molecular mechanisms of amyloidosis

- vpc.lt [PDF] 
G Merlini, V Bellotti - The New England journal of medicine, 2003 - nejm.highwire.org
The amyloidoses constitute a large group of diseases in which misfolding of
extracellular protein has a prominent role. This dynamic process, which occurs
in parallel with or as an alternative to physiologic folding, generates ...
Cited by 410 - Related articles - BL Direct - All 9 versions

High-dose melphalan and autologous stem-cell transplantation in patients with AL …

- annals.org [PDF] 
M Skinner, V Sanchorawala, DC Seldin, LM … - Annals of internal medicine, 2004 - Am Coll Physicians
Martha Skinner, MD; Vaishali Sanchorawala, MD; David C. Seldin, MD, PhD; Laura
M. Dember, MD; Rodney H. Falk, MD; John L. Berk, MD; Jennifer J. Anderson, PhD;
Carl O'Hara, MD; Kathleen T. Finn, RN, NP; Caryn A. Libbey, MD; Janice ...
Cited by 259 - Related articles - All 17 versions

Tolerability and efficacy of thalidomide for the treatment of patients with light chain– …


DC Seldin, EB Choufani, LM Dember, JF … - Clinical Lymphoma & Myeloma, 2003 - CIG Media Group
Introduction In light chain–associated (AL) amyloidosis, immunoglobulin light
chains are deposited in tissues as fibrils leading to tissue damage and
multiorgan dysfunction. Organ failure is progres- sive and the median ...
Cited by 76 - Related articles - BL Direct - All 2 versions

Prognostication of survival using cardiac troponins and N-terminal pro-brain natriuretic …

- hematologylibrary.org - Free from Publisher
A Dispenzieri, MA Gertz, RA Kyle, MQ Lacy, … - Blood, 2004 - bloodjournal.hematologylibrary.org
Primary systemic amyloidosis (AL) is a fatal plasma cell disorder. Pilot data
suggest survival is better in patients undergoing peripheral blood stem cell
transplantation (PBSCT), but the selection process makes the apparent ...
Cited by 75 - Related articles - BL Direct - All 8 versions

High-dose intravenous melphalan and autologous stem cell transplantation as initial therapy …


V Sanchorawala, DG Wright, DC Seldin, RH … - Bone Marrow Transplantation, 2003 - nature.com
A prospective randomized trial was conducted to study the timing of high-dose
intravenous melphalan and autologous stem cell transplantation (HDM/SCT) in AL
amyloidosis. In all, 100 newly diagnosed patients were randomized to ...
Cited by 65 - Related articles - BL Direct - All 3 versions

Risk-adjusted manipulation of melphalan dose before stem cell transplantation in patients …


MA Gertz, MQ Lacy, A Dispenzieri, SM Ansell, … - Bone Marrow Transplantation, 2004 - nature.com
High-dose chemotherapy and autologous stem cell transplantation are used
increasingly to treat patients with light-chain-related amyloidosis (AL).
Treatment-related mortality is approximately 15%. To enable more patients ...
Cited by 52 - Related articles - BL Direct - All 3 versions

Improvement in quality of life of patients with AL amyloidosis treated with high-dose …


DC Seldin, JJ Anderson, V Sanchorawala, K … - Blood, 2004 - bloodjournal.hematologylibrary.org
Treatment of AL amyloidosis patients with high-dose melphalan chemotherapy
followed by autologous peripheral blood stem cell transplantation (HDM/SCT) can
produce hematologic complete responses (CRs) and improvement in organ ...
Cited by 50 - Related articles - BL Direct - All 14 versions

Eprodisate for the treatment of renal disease in AA amyloidosis

- ucl.ac.uk [PDF] 
LM Dember, PN Hawkins, BPC Hazenberg, PD … - New England Journal of Medicine, 2007 - content.nejm.org
From Boston University School of Medi- cine, Boston (LMD, MS); the National
Amyloidosis Centre, Royal Free Hospital, London (PNH, HJL); the University
Medical Center Groningen, University of Groningen, Groningen, the ...
Cited by 48 - Related articles - BL Direct - All 11 versions

Amyloidosis-associated kidney disease

- asnjournals.org
LM Dember - Journal of the American Society of Nephrology, 2006 - Am Soc Nephrol
The amyloidoses are a group of disorders in which soluble proteins aggregate and
deposit extracellularly in tissues as insoluble fibrils, causing progressive
organ dysfunction. The kidney is one of the most frequent sites of amyloid ...
Cited by 39 - Related articles - BL Direct - All 7 versions

Therapy for immunoglobulin light chain amyloidosis: the new and the old


MA Gertz, MQ Lacy, A Dispenzieri - Blood reviews, 2004 - Elsevier
An accurate diagnosis of amyloidosis and its subtype classification are
essential for disease prognostication and treatment. In primary amyloidosis,
overall median survival is approximately 2 years and may be less in ...
Cited by 34 - Related articles - All 12 versions


Result Page: 

1

2

3

4

5

6

7

Next


 


Go to Google Home - About Google - About Google Scholar

©2009 Google