Results 61 to 70 of about 6,925 (157)

Algorithms in Allergy: Diagnosis of Hypereosinophilic Syndromes, 2026 Update

Allergy, EarlyView.
Guillaume Lefèvre, Florence Roufosse, Giacomo Emmi, Andreas Reiter, Emmanuel Ledoult, Jean‐Emmanuel Kahn   +5 more
wiley   +1 more source

Kyphoscoliosis as a skeletal malformation in a domestic corn snake (Pantherophis guttatus)

Veterinary Record Case Reports, Volume 14, Issue 3, August 2026.
Abstract Skeletal malformations in snakes represent an intriguing yet challenging aspect of veterinary medicine, as they can lead to significant impairment of patients’ mobility and therefore to poor quality of life. Reported skeletal malformations include proliferative osteoarthritis, osteoarthrosis, metabolic bone disease, Paget's disease or ...
Milena Tegelkamp, Eva Dervas, Katarzyna Walczak, Eva Maria Dutitre, Francesca Del Chicca   +4 more
wiley   +1 more source

Hypereosinophilia in patients with multiple sclerosis treated with natalizumab

, 2011
To report asymptomatic hypereosinophilia as a potential side effect in patients treated with natalizumab, an α-4 integrin blocking ...
Ribi, Camillo, Abbas, Mohamed, Simon, H-U, Chofflon, Michel, Chizzolini, Carlo, Lalive d'Epinay, Patrice   +5 more
core   +1 more source

Targeting Immunologic Pathways in Eosinophilic Granulomatosis With Polyangiitis: Translating Emerging Evidence Into Clinical Practice

Allergy, Volume 81, Issue 8, Page 2775-2791, August 2026.
ABSTRACT Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare and potentially life‐threatening systemic, inflammatory disease with multi‐organ manifestations, variable presentation and complex pathology. Multiple interconnected immunological pathways are implicated in EGPA pathology, including a type‐2 immune response driving predominantly ...
Harold Wilson‐Morkeh, Lior Seluk, Philipp Bosch, Carolina Aguiar, Jens Thiel, Bernhard Hellmich, Michael E. Wechsler, Salman Siddiqui   +7 more
wiley   +1 more source

An unusual presentation of osteochondrosis in the elbows and tarsi of a Friesian colt

Equine Veterinary Education, Volume 38, Issue 8, Page e464-e471, August 2026.
Summary This case report describes the clinical, diagnostic imaging results and post‐mortem findings in a foal that underwent reassessment following surgical management of angular limb deformities (ALD) and acute onset of gait abnormalities. Upon presentation, the foal showed an abnormal stiff gait characterised by bilateral medial limb collapse during
A. Torrent‐Crosa, A. Merchán‐Muñoz, C. Co, E. Borkowski   +3 more
wiley   +1 more source

Severe persistent hypereosinophilia of undetermined significance: diagnostic challenges in clinical practice and two-year follow-up

Romanian Journal of Internal Medicine
Hypereosinophilia of undetermined significance (HE-US) represents a rare subtype of hypereosinophilia (HE) defined by a persistent absolute eosinophil count (AEC) ≥ 1500/uL without an identifiable reactive or clonal cause, and importantly, without ...
Leru Polliana Mihaela, Anton Vlad Florin, Georgescu Daniela Georgeta   +2 more
doaj   +1 more source

Biomarkers for therapeutic response and adverse outcomes in atopic dermatitis: A systematic review

Journal of the European Academy of Dermatology and Venereology, Volume 40, Issue 7, Page 1173-1184, July 2026.
This review assessed 52 biomarkers predicting systemic therapy response and adverse events in atopic dermatitis. Most studies focused on dupilumab, and findings were inconsistent. IgE and eosinophils were largely non‐predictive, though elevated eosinophils and LDH sometimes indicated poorer outcomes.
Eva Hilger, Kaitlyn Chan, Alphonsus Yip, Xingyue Maria Wang, Conor Broderick, Bernd Arents, Karin van Bart, Kilian Eyerich, Joseph Rastrick, Stephan Weidinger, Carsten Flohr, on behalf of the BIOMAP Consortium   +11 more
wiley   +1 more source

A new case of t(5;14)(q31;q32) in a pediatric acute lymphoblastic leukemia presenting with hypereosinophilia [PDF]

, 2012
Case report of a translocation : A new case of t(5;14)(q31;q32) in a pediatric acute lymphoblastic leukemia presenting with ...
Gallego, M, Coccé, M, Alonso, C, Felice, M, Rossi, J, Eandi, S, Sciuccati, G   +6 more
core   +1 more source

Multiple Cerebral Infarcts and Encephalopathy as the First Clinical Manifestations of Hypereosinophilic Syndrome: A Case Report and Narrative Review

Pulse
Background: Hypereosinophilic syndrome is characterized by a peripheral blood eosinophil count >1.5 × 103/μL on two different examinations within a month of each other and/or a 20% or higher percentage of eosinophils in a bone marrow section ...
Sonia Romano, Giulia Avola, Marco Cesare Angeli, Francesca Brazzale, Elena Giacopazzi, Paola Castellini, Antonio Genovese   +6 more
doaj   +1 more source

Efficacy and Safety of Mepolizumab (Anti-Interleukin-5) Treatment in Gleich’s Syndrome

Frontiers in Immunology, 2018
Gleich’s syndrome (GS) is characterized by recurrent episodes of angioedema, increase in body weight, fever, hypereosinophilia, and elevated serum IgM. The exact etiology remains unclear.
Andrea Matucci, Francesco Liotta, Emanuele Vivarelli, Laura Dies, Francesco Annunziato, Marie Pierre Piccinni, Francesca Nencini, Sara Pratesi, Enrico Maggi, Alessandra Vultaggio   +9 more
doaj   +1 more source