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POEMS syndrome

Blood Reviews, 2005
Abstract POEMS syndrome is defined by the presence of a peripheral neuropathy (P), a monoclonal plasma cell disorder (M), and other paraneoplastic features, the most common of which include organomegaly (O), endocrinopathy (E), skin changes (S), papilledema, edema, effusions, ascites, and thrombocytosis.
openaire   +3 more sources

Single‐agent daratumumab for refractory POEMS syndrome

American journal of hematology/oncology, 2022
To the Editor: Existing literature on daratumumab, a fully human IgG1 κ monoclonal antibody directed against CD38, in POEMS syndrome is limited. POEMS syndrome is a plasma cell disorder presenting typically with polyradiculoneuropathy (P), organomegaly ...
Han Wei Tiew   +8 more
semanticscholar   +1 more source

[POEMS syndrome].

La Revue du praticien, 2007
Olivier, Fain   +2 more
openaire   +3 more sources

An open‐label, prospective trial to evaluate the efficacy and safety of ixazomib in combination with cyclophosphamide and dexamethasone in patients with newly diagnosed POEMS syndrome

British Journal of Haematology
This open‐label, prospective trial evaluated the combination of ixazomib, cyclophosphamide and dexamethasone (ICD) in 12 newly diagnosed POEMS syndrome patients. The study is registered with the Chinese Clinical Trials Registry (ChiCTR2000030072).
Haiyan He   +8 more
semanticscholar   +1 more source

A POEMS syndrome patient with idiopathic non-cirrhotic portal hypertension received the transjugular intrahepatic portosystemic shunt: a case report and literature review

Nigerian Journal of Clinical Practice, 2022
Polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes (POEMS) syndrome is a rare plasma cell dyscrasia disease involving multiple organs combined with idiopathic non-cirrhotic portal hypertension.
Y. Chen   +4 more
semanticscholar   +1 more source

POEMS syndrome.

Connecticut medicine, 2004
A middle-aged man presented with progressive dyspnea and a pleural effusion. He had slowly progressive bilateral symmetric extremity weakness, mediastinal lymphadenopathy, and splenomegaly. The diagnosis of POEMS syndrome (Polyneuropathy, Organomegaly, Endocrinopathy, M-Protein and Skin changes was suspected clinically and confirmed with a bone marrow ...
Mark, Goldstein, Tapas, Bandyopadhyay
openaire   +3 more sources

Prevalence, clinical profiles, and prognosis of POEMS syndrome in Japanese nationwide survey

Neurology, 2019
Objective To elucidate current epidemiological, clinical profiles, and treatment of polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome.
T. Suichi   +11 more
semanticscholar   +1 more source

[POEMS syndrome].

Presse medicale (Paris, France : 1983), 1994
POEMS syndrome has been defined as an association of plasma cell dyscrasia with polyneuropathy, organomegaly, endocrinopathy, M protein and skin changes. Although certain authors do not distinguish this syndrome from osteosclerosing myeloma, syndromes comparable to POEMS have been observed without bone lesions.
C, Masson, Y, Krespi
openaire   +1 more source

Sindrom POEMS: POEMS syndrome:

2008
Background We have presented the patient with POEMS syndrome (Polyneuropathy, Organo megaly, Endocrinopathy, M protein, Skin changes) in which peripheral neuropathy was associated with monoclonal gammopathy and osteosclerotic myeloma. The clinical picture, diagnostic procedures, the course of the disease and the treatment are discussed.
Černelč, Peter, Luštrek, Bojana
openaire   +1 more source

POEMS-Syndrom

RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren, 2018
Ricarda, Schwarz, Marius, Horger
openaire   +2 more sources

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