Results 151 to 160 of about 124,392 (280)

Atypical Persistent Pruritic Hyperpigmented Plaques in Adult‐Onset Still's Disease: A Case Report From Uganda

Clinical Case Reports, Volume 14, Issue 5, May 2026.
Atypical Persistent hyperpigmented cutaneous lesions associated with adult‐onset Still's disease. ABSTRACT We report a case of adult‐onset Still's disease (AOSD) in a 30‐year‐old Ugandan man presenting with migratory polyarthralgia, intermittent fever, lymphadenopathy, and atypical persistent pruritic hyperpigmented plaques.
Abdisalam Ahmed Sandeyl, Stephen Kizito Mirembe, Kusemererwa Byaruhanga, Farah Dubad Abdi, Abdisamad Guled Hersi, Louis K. Kamyuka, Venance Emmanuel Mswelo, Rawan Yousif Hassan   +7 more
wiley   +1 more source

Analysis of Real‐World Data Utilization in the Orphan Drug Approval Process: Focusing on New Drug Marketing Applications Submitted to the FDA

Clinical Pharmacology &Therapeutics, Volume 119, Issue 5, Page 1340-1349, May 2026.
In the field of rare diseases—where traditional clinical trials are often impractical—real‐world data (RWD) have emerged as a scientifically valid alternative to support regulatory decision making. This study systematically evaluates the utilization of RWD in orphan drug approvals by the FDA Center for Drug Evaluation and Research (CDER) over the past ...
Minji Kim, Eunjin Hong
wiley   +1 more source

Group A β-hemolytic streptococcus causing purpura fulminans: two case reports. [PDF]

Front Immunol
Alkhatatbeh A, Chen J, Chen Y, Ma Z, Chen H, Chen B, Zhou Y, Xia X, Huang X, Hong S, Hu J.   +10 more
europepmc   +1 more source

Engineering, Expression, Purification, and Application of Glycosaminoglycan‐Specific Antibodies

Current Protocols, Volume 6, Issue 5, May 2026.
Abstract Cluster of differentiation markers have been transformative for defining cell populations and their functional states, but recent work indicates that finer granularity can be achieved by considering the diverse heparan sulfate structures presented on proteoglycans.
Kheerthana Duraivelan, Sriram Sundaravel, Esther N. Njoroge, Robert A. Townley, Ulrich G. Steidl, Hannes E. Bülow, Steven C. Almo, Scott J. Garforth   +7 more
wiley   +1 more source

Systematic Literature Review of the Economic and Quality of Life Burden of Congenital and Immune-Mediated Thrombotic Thrombocytopenic Purpura. [PDF]

J Blood Med
Kaur H, Ghoshal D, Khurana IS.
europepmc   +1 more source

Leukocytoclastic vasculitis and necrobiotic pulmonary nodules in endoscopic remission of ulcerative colitis

JPGN Reports, Volume 7, Issue 2, Page 309-311, May 2026.
Abstract Skin and lung findings, including the rare findings of leukocytoclastic vasculitis (LCV) and necrobiotic pulmonary nodules, are known extraintestinal manifestations (EIMs) of inflammatory bowel disease. However, these rare EIMs have typically been reported as being a sign of active intestinal disease.
Joshua D. Noe, James Bistolarides, Karolyn A. Wanat, Yvonne Chiu   +3 more
wiley   +1 more source

Acute Myocardial Infarction Due to Eltrombopag Therapy in a Patient with Immune Thrombocytopenic Purpura

Turkish Journal of Hematology, 2017
Sena Sert, Hasan Özdil, Murat Sünbül
doaj   +1 more source

Diffuse purpuric eruption in a patient with acute myeloid leukemia

JAAD Case Reports, 2023
Zoha K. Momin, BS, Aya Alame, MD, Travis Vandergriff, MD, Cristina Thomas, MD, Kaveh Nezafati, MD   +4 more
doaj   +1 more source

Cutaneous leukocytoclastic vasculitis mimicking IgA vasculitis in a patient with intestinal Behçet's disease: a diagnostic challenge. [PDF]

An Bras Dermatol
Nakamura T, Chen KR, Yamamoto T.
europepmc   +1 more source

Microscopic Polyangiitis After Pulmonary Nontuberculous Mycobacterial Disease: A Case Report and Literature Review

Respirology Case Reports, Volume 14, Issue 5, May 2026.
This case highlights that ANCA‐associated vasculitis can emerge in patients with chronic airway disease and a history of nontuberculous mycobacterial infection, potentially masquerading as infection‐related inflammation. Early recognition based on extrapulmonary clues (urinary abnormalities and neuropathy) enabled prompt diagnosis and treatment with ...
Hidenori Takahashi, Riho Nakagawa, Mio Toyama‐Kousaka, Yugo Satake, Hiroki Nagamatsu, Ryutaro Hirose, Naoya Toba, Shinichiro Ota, Miwa Morikawa, Natsuko Nakano, Kazuyoshi Ishigaki, Masaharu Shinkai   +11 more
wiley   +1 more source