Results 51 to 60 of about 1,326,560 (112)
A Quarter Century of EHD Protein Research: From Endosomal Recycling to Ciliopathies
Traffic, Volume 27, Issue 3, September 2026.Human EHD protein subcellular localization. ABSTRACT Eps15 homology domain‐containing proteins comprise a conserved family of membrane‐remodeling ATPases that regulate endocytic trafficking, membrane fission, receptor recycling, primary ciliogenesis and membrane dynamics across eukaryotes. Since the initial identification of EHD1 and its Caenorhabditis
Devin Frisby +3 more
wiley +1 more source
Product-oriented environmental management system (POEMS): a sustainable management framework for the food industry [PDF]
, 2011 : POEMS is a new tool designed to bring together traditional environmental management systems and tools oriented to the environmental evaluation of products.
Salomone, Roberta +2 more
core
British Journal of Haematology, Volume 209, Issue 2, Page 755-759, August 2026.Glomeruloid haemangiomas and extensive angiomas occurred in a small subset of Erdheim–Chester disease patients, all showing markedly elevated vascular endothelial growth factor‐A (VEGF‐A) levels despite the absence of POEMS (polyneuropathy, organomegaly, M‐spike, and skin disease) syndrome.
Jerome Razanamahery +10 more
wiley +1 more source
Immunophenotypic characteristics of plasma cells in POEMS syndrome
Cytometry Part B: Clinical Cytometry, Volume 110, Issue 4, Page 266-273, July 2026.Abstract To analyze the immunophenotypic characteristics of plasma cells in patients with polyneuropathy, organomegaly, endocrinopathy, myeloma protein, and skin changes (POEMS) syndrome. This retrospective study included patients with POEMS syndrome hospitalized in the Department of Hematology, Huashan Hospital, from September 2017 to August 2025 ...
Zhenhua Wang +6 more
wiley +1 more source
BMC NeurologyBackground Both vitamin B6 deficiency and vitamin B12 deficiency can present with symptoms that appear like polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes (POEMS) syndrome, with painful peripheral neuropathy and sensorimotor ...
Stephan Hu +3 more
doaj +1 more source
Online Journal of Health & Allied Sciences, 2021 POEMS syndrome is a rare multisystem paraneoplastic disease that manifests with a spectrum of symptoms namely peripheral neuropathy (P), organomegaly (O), endocrinopathy (E) monoclonal plasma-cells proliferative disorder (M) and skin changes (S).
Cynthia Amrutha Sukumar +3 more
doaj
Pituitary Tumour Apoplexy as Cause of Death of Simonetta Vespucci, the Venus by Botticelli
Endocrinology, Diabetes &Metabolism, Volume 9, Issue 4, July 2026.A reassessment of Simonetta Vespucci, muse of Sandro Botticelli, attributes her long‐mysterious death to a pituitary adenoma. Clinical reinterpretation of historical accounts suggests tumour expansion led to sellar destruction, severe haemorrhage, and pulmonary complications, offering a coherent medical explanation for her sudden death at twenty‐three.
Domiziana Nardelli +3 more
wiley +1 more source
Case report: POEMS syndrome in childhood
, 2008 POEMS syndrome is a rare multisystem disorder, which is characterized by polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes.
Hatipoglu, Sami +4 more
core +1 more source
European Journal of Case Reports in Internal MedicineIntroduction: Autoimmune cytopenias have been very rarely reported in conjunction with POEMS (polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes syndrome).
Mohamed Reda Belkhribchia +6 more
doaj +1 more source