Results 161 to 170 of about 1,385 (194)
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877 | SPANISH IDIOPATHIC MULTICENTRIC CASTLEMAN DISEASE REGISTRY. EPIDEMIOLOGY OF IMCD IN SPAIN (ARCANA)—PREVALENCE COHORT

Hematological Oncology
J. T. Navarro Ferrando   +15 more
openaire   +2 more sources

POS0380 SPANISH iMCD REGISTRY EPIDEMIOLOGY OF IDIOPATHIC MULTICENTRIC CASTLEMAN DISEASE IN SPAIN (ARCANA) - PREVALENCE COHORT

Annals of the Rheumatic Diseases
A. González García   +4 more
openaire   +2 more sources

Somatic mutation discovery in idiopathic multicentric castleman disease (iMCD) lymph node tissue identifies dysregulated intracellular calcium signaling as a potential disease mechanism and therapeutic target

Blood
Background: Idiopathic multicentric Castleman disease (iMCD) is a rare, atypical lymphoproliferative disorder with significant morbidity and mortality and unknown etiology.
Michael V. Gonzalez   +13 more
semanticscholar   +1 more source

Retrospective real-world data analysis of morbidity burden and healthcare costs in idiopathic multicentric castleman disease compared with matched controls (BURDEN-iMCD)

Blood
Introduction: Idiopathic multicentric Castleman disease (iMCD) is a rare, cytokine-driven hematologic disorder characterized by diffuse lymphadenopathy and systemic inflammation.
A. Noy   +10 more
semanticscholar   +1 more source

Prognostic value of serum C-reactive protein in idiopathic multicentric Castleman disease and construction of a prognostic model for patients

Frontiers in Medicine
Background Idiopathic Multicentric Castleman disease (iMCD) is a type of the rare lymphoproliferative diseases. C-reactive protein (CRP) is a well-recognized biomarker of inflammation, frequently exhibits elevated levels in individuals diagnosed with ...
Zhixiang Lei   +9 more
semanticscholar   +1 more source

33 A Rare Case of Idiopathic Multicentric Castleman Disease with Ocular Involvement

American Journal of Clinical Pathology
Idiopathic multicentric Castleman disease (iMCD) is a benign lymphoproliferative disorder with uncertain etiology, as opposed to other forms such as Kaposi sarcoma-associated / human herpesvirus 8 (KSHV/HHV8)-associated multicentric Castleman ...
Alexander Yue, Daniel Ding
semanticscholar   +1 more source

Striking effectiveness of siltuximab-based treatment in refractory idiopathic multicentric Castleman disease resembling IgG4-related disease.

Journal of chemotherapy
Castleman disease (CD) and immunoglobulin G4-related disease (IgG4-RD) are rare systemic immune-mediated disorders that share similar clinical manifestations and overlapping pathological features. We present a case of insidious idiopathic multicentric CD
Xing Gong   +3 more
semanticscholar   +1 more source

Increased type I interferon signaling is a hallmark of idiopathic multicentric castleman disease

Blood
Human herpesvirus (HHV)-8-negative, idiopathic multicentric Castleman disease (iMCD) is a rare hematologic illness involving progressive flares of inflammation, lymphoproliferation, and cytokine-induced organ failure. While there is an FDA-approved
Katherine S. Forsyth   +4 more
semanticscholar   +1 more source

Idiopathic multicentric castleman disease - tafro: A potentially curable disease?

Blood
Idiopathic multicentric Castleman disease (iMCD) is a group of rare and sometimes life-threatening hematological disorders.The Castleman Disease Collaborative Network (CDCN) consensus for treating iMCD has been reached since 2018 and iMCD is ...
Lu Zhang   +4 more
semanticscholar   +1 more source

Siltuximab-mediated suppression of CRP is associated with clinical response in idiopathic multicentric castleman disease

Blood
Introduction Idiopathic multicentric Castleman disease (iMCD) is a rare and serious disorder involving multicentric lymphadenopathy, systemic inflammation, and cytokine-driven organ dysfunction.
Jean-Franc¸ois Rossi   +5 more
semanticscholar   +1 more source

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