Results 51 to 60 of about 2,670,869 (240)

Poetry, resistance, world-literature : Adília Lopes and Marie Buck [PDF]

, 2019
This essay begins an exploration of how poetry functions within the field of world-literature, drawing specifically on the Warwick Research Collective’s Combined and Uneven Development: Towards a New Theory of World-Literature and reflecting ...
de Medeiros, Paulo
core   +1 more source

Comprehensive Diagnosis and Management of POEMS Syndrome

HemaSphere, 2022
Polyneuropathy Organomegaly, Endocrinopathy, Monoclonal protein and Skin changes syndrome is a rare multisystem condition with a range of manifestations which are often overlooked as trivial comorbidities, until their whole triggers the possibility of ...
S. D’Sa, J. Khwaja, S. Keddie, Ryan Keh, D. Smyth, Ruth Ronneberger, S. Dubash, Suganya Sivabalasingham, S. Wan, C. Hoskote, S. Baldeweg, J. Sive, M. Lunn   +12 more
semanticscholar   +1 more source

Peripheral retinal leakage in POEMS syndrome

International Journal of Retina and Vitreous, 2021
Background POEMS (polyneuropathy, organomegaly, endocrinopathy, myeloma protein, skin changes) syndrome is a rare blood disorder with multi-system involvement. The cause is unknown.
Andrew Rising Carey, Praveen Jeyaseelan
doaj   +1 more source

POEMS syndrome with extensive calciphylaxis: A case report and literature review

Indian Journal of Dermatology, 2020
POEMS syndrome, a paraneoplastic disorder, caused by plasma cell dyscrasia, is characterized by polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes.
Cheng-Han Liu, Yu-Chen Chen, Tsai-Yun Chen, Hang-Wei Huang, Julia Yu-Yun Lee   +4 more
doaj   +1 more source

Raynaud’s phenomenon and positive antinuclear antibodies as first manifestation of POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes): a case report

BMC Rheumatology, 2022
Background POEMS syndrome is a rare paraneoplastic syndrome caused by plasma cell disorder almost always lambda restricted. Secondary Raynaud’s phenomenon is an overlooked skin manifestation of the disease even though it is present in twenty percent of ...
Fabio Torres-Saavedra, Lina León-Sierra
doaj   +1 more source

Daratumumab–bortezomib–dexamethasone use in relapsed POEMS syndrome

eJHaem, 2022
POEMS syndrome is a rareparaneoplastic disorder driven by an underlying low level plasma cell dyscrasiaand associated with elevated serum vascular endothelial growth factor (VEGF).
J. Khwaja, Ryan Keh, D. Smyth, M. Lunn, S. D’Sa, J. Sive   +5 more
semanticscholar   +1 more source

Polyneuropathy as Novel Initial Manifestation in a Case of “Nonsecretory” POEMS Syndrome with Sjögren’s Syndrome

Case Reports in Medicine, 2017
POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes) is a paraneoplastic syndrome driven by plasma cell dyscrasias.
Minrui Liang, Zhixing Jiang, Zhiguang Lin, Bobin Chen, Hejian Zou, Weiguo Wan, Jun Liu   +6 more
doaj   +1 more source

Shoah in Marian Pankowski’s Literary Art [PDF]

, 2016
The article centers on the theme of the Holocaust in the literary works of Marian Pankowski: its sources, relations with the concentration camp theme, particular works and their poetics, as well as the aesthetic, social and political problems related to ...
Morawiec, Arkadiusz
core   +2 more sources

Lenalidomide and Dexamethasone for a Patient of POEMS Syndrome Presenting with Massive Ascites

Case Reports in Hematology, 2014
POEMS syndrome is a multisystem disorder characterized by polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes. POEMS syndrome is a rare cause of refractory ascites.
Shuji Ueda, Sayoko Yonemoto, Kazumasa Oka, Naohiko Fujii, Keiichi Nakata, Hitomi Matsunaga, Seiko Kataoka, Yuki Iwama, Hiroyuki Narahara, Yuichi Yasunaga, Yoshiaki Inui, Sumio Kawata   +11 more
doaj   +1 more source

POEMS Syndrome: Real World Experience in Diagnosis and Systemic Therapy - 108 Patients Multicenter Analysis.

Clinical Lymphoma, Myeloma & Leukemia, 2021
POEMS syndrome, a rare plasma cell disorder, is challenging both in the diagnostic and therapeutic management. We present real word retrospective analysis of 108 cases analyzing clinical features and therapeutic modes.
A. Jurczyszyn, J. Castillo, M. Olszewska-Szopa, L. Kumar, S. Thibaud, J. Richter, Karin Flicker, M. Fiala, R. Vij, S. Yi, Fang Xu, R. Silbermann, C. Gaisán, E. Ocio, A. Waszczuk-Gajda, E. Crusoé, Aleksander Salomon-Perzyński, I. Hus, J. D. Valls, A. Gozzetti, J. Czepiel, K. Krzanowska, A. Chappell, S. Chellapuram, A. Suska, D. Vesole   +25 more
semanticscholar   +1 more source