Results 61 to 70 of about 4,496 (202)

Simultaneous tDCS‐rTMS stimulation to regulate the language network and improve language ability in Landau–Kleffner syndrome

Epilepsia Open, Volume 10, Issue 6, Page 1997-2008, December 2025.
Abstract Landau–Kleffner syndrome (LKS) is a rare epileptic syndrome causing language regression. In this preliminary study, we investigated the effects of simultaneous transcranial direct current stimulation (tDCS) and transcranial magnetic stimulation (rTMS) on LKS patients and the underlying mechanism based on magnetoencephalography (MEG) network ...
Runze Chen, Xinyan Liu, Xiaohong Qi, Wenwen Shen, Xuerong Leng, Xiating Zhang, Liping Zhang, Yuexin Zhang, Xuan Zhao, Xingyu Wang, Jicong Zhang, Yuping Wang, Yicong Lin   +12 more
wiley   +1 more source

Clinical Presentation, Treatment, and Outcomes of 28 Patients With Castleman Disease: A Retrospective Analysis of an Italian Cohort

eJHaem, Volume 6, Issue 6, December 2025.
ABSTRACT Background Castleman disease (CD) encompasses a range of heterogeneous non‐clonal lymphoproliferative disorders, including unicentric (UCD), and multicentric (MCD) forms. The latter is subdivided into HHV‐8+ MCD, POEMS‐MCD, and idiopathic‐MCD, not otherwise specified (iMCD‐NOS).
Caterina Cristinelli, Michele Merli, Marco Lucioni, Manuel Gotti, Roberta Sciarra, Sara Rattotti, Federico Carpi, Gianmarco Favrin, Benedetta Bianchi, Giuseppe Neri, Marta Coscia, Marcello Gambacorta, Francesco Passamonti, Marco Paulli, Luca Arcaini   +14 more
wiley   +1 more source

Cerebral large artery stenosis and occlusion in POEMS syndrome [PDF]

, 2021
Atsuhiko Sugiyama, Hajime Yokota, Sonoko Misawa, Hiroki Mukai, Yukari Sekiguchi, Kyosuke Koide, Tomoki Suichi, Jun Matsushima, Takashi Kishimoto, Zen‐ichi Tanei, Yuko Saito, Shoichi Ito, Satoshi Kuwabara   +12 more
openalex   +1 more source

Multiple Myeloma in Young Adults—Insights From a Tertiary Care Cancer Centre in India

eJHaem, Volume 6, Issue 6, December 2025.
ABSTRACT Background Multiple myeloma (MM) is primarily a disease of the elderly; data on young patients are limited. Aim To evaluate the clinical characteristics and outcomes of MM patients aged ≤$ \le $ 40 years. Methods We retrospectively analyzed newly diagnosed MM patients aged ≤ 40 years between 2013 and 2021.
George John, Sumeet Mirgh, Sachin Punatar, Nishant Jindal, Lingaraj Nayak, Akanksha Chichra, Alok Shetty, Anant Gokarn, Sweta Rajpal, Nikhil Patkar, Gaurav Chatterjee, Dhanalaxmi Shetty, Hemani Jain, Kinjalka Ghosh, Prashant Tembhare, Hasmukh Jain, Akash Pawar, Sumeet Gujral, Papagudi Subramaniam, Manju Sengar, Navin Khattry, Bhausaheb Bagal   +21 more
wiley   +1 more source

Endocrine Manifestations in POEMS Syndrome: a case report and literature review

BMC Endocrine Disorders, 2019
Background POEMS syndrome, a rare systemic disease, is characterized by 5 components: Peripheral neuropathy, Organomegaly, Endocrinopathy, M protein elevation, and Skin changes.
Hui Li, Yumeng Huang, Yan Li, Baozhong Zheng, Jingqiu Cui, Ming Liu   +5 more
doaj   +1 more source

A Career as a Participatory Teacher in Hungarian Higher Education

British Journal of Learning Disabilities, Volume 53, Issue 4, Page 487-497, December 2025.
ABSTRACT Background Under the Convention on the Rights of Persons with Disabilities, disabled people have the right to participate in all decisions that affect their lives, be they in any segment of legislation, policy or practice. The academic world is no exception.
Anikó Sándor, Csilla Cserti‐Szauer, András Futár, György Könczei   +3 more
wiley   +1 more source

Castleman disease of the hyaline vascular variant transforming to POEMS syndrome as endpoint: a case report

BMC Neurology, 2018
Background POEMS syndrome is a rare neoplastic syndrome reflected by plasma cell disorder. It is composed by polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes. It is also reported to associate with Castleman disease.
Yijun Ge, Qian Da, Ying Dai
doaj   +1 more source

POEMS syndrome characterized by peripheral neuropathy as the first symptom: a rare case report

, 2022
Meng Li, Ying Zuo
openalex   +1 more source

POEMS syndrome with undetectable M-protein: a case report and literature review

Diagnostic Pathology
Background Polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome is a rare plasma cell (PC) neoplasm with associated paraneoplastic syndrome. According to the current diagnostic criteria, peripheral polyneuropathy and
Han-Yue Xue, Lin Zhou, Qin-Zhao Yuan, Yang Zhang, Yi-Qun Hao, Shao-Wei Chen, Hong-Kun Wang, Fang Wei   +7 more
doaj   +1 more source

Síndrome de POEMS (mieloma osteoesclerótico) POEMS syndrome (osteosclerotic myeloma)

Revista Brasileira de Hematologia e Hemoterapia, 2007
A síndrome de POEMS é uma entidade clínica única definida pela presença concomitante de doença monoclonal de plasmócitos, polineuropatia periférica e outras manifestações paraneoplásicas tais como organomegalias, endocrinopatias, alterações cutâneas ...
Jorge V. Pinto Neto
doaj   +1 more source