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Update on the Diagnosis and Treatment of POEMS (Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Changes) Syndrome: A Review.

JAMA Oncology, 2021
Importance POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes) syndrome is a rare plasma cell disorder characterized by demyelinating peripheral neuropathy and clonal plasma cell proliferation.
Jack Khouri, M. Nakashima, S. Wong
semanticscholar   +1 more source

What is the best first-line treatment for POEMS syndrome: autologous transplantation, melphalan and dexamethasone, or lenalidomide and dexamethasone?

open access: yesLeukemia, 2019
POEMS syndrome is a rare plasma cell dyscrasia. This study compared the responses to and survival of 347 POEMS syndrome patients given three first-line treatment regimens: autologous stem cell transplantation (ASCT, N = 165) and melphalan + dexamethasone
Hao Zhao, Xu-fei Huang, Xue-Min Gao
exaly   +2 more sources

Bread and wine in Lycian poetry. A contextual interpretation of TL 44c

Kadmos, 2021
In the following paper, new meanings for the Lycian B words waxssa, mur(i)- (and murei(je)-) and tubur(i)- are suggested using the combinatorial and etymological methods.
D. Sasseville
semanticscholar   +1 more source

Clinical characteristics, risk factors, and outcomes of POEMS syndrome

Neurology, 2020
Objective POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin lesions) is a paraneoplastic disorder resulting in severe neurologic disability.
S. Keddie   +16 more
semanticscholar   +1 more source

POEMS syndrome: clinical update

open access: yesJournal of Neurology, 2018
POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes) is a rare paraneoplastic syndrome, caused by a plasma cell proliferative disorder, which is most commonly lambda restricted. The neurological hallmark, which forms one
Rachel Brown
exaly   +2 more sources

Selected Poems

Comedy, 2019
This Individual Article is brought to you for free and open access by Scholars Crossing. It has been accepted for inclusion in The Kabod by an authorized editor of Scholars Crossing. For more information, please contact scholarlycommunication@liberty.edu.
Gwendolyn Brooks
semanticscholar   +1 more source

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: A multisystem clonal disorder

European Journal of Haematology, 2020
Polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes (POEMS) syndrome is a rare condition defined by monoclonal plasma cell disorder, peripheral neuropathy, and other systemic symptoms.
Tayyaba Ali, M. Qazilbash
semanticscholar   +1 more source

The Tradition of Quoting Homer as a Way of Identification in the Inscriptions of Southern Asia Minor

Вестник Пермского университета. Российская и зарубежная филология
After the conquests of Alexander the Great, many Greeks migrated to the southern regions of Asia Minor, including Lycia, Pisidia, Pamphylia, and Cilicia. They brought along their cultural traditions, which gradually merged over several centuries with the
Elena V. Prikhodko
semanticscholar   +1 more source

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