Results 111 to 120 of about 13,293,436 (201)
What Is Your Diagnosis? Blood Smear From a Mixed‐Breed Dog
Veterinary Clinical Pathology, EarlyView.
Laura S. Peres +5 more
wiley +1 more source
Depigmentation Outcomes in Pigmented Oral Lichen Planus Managed With Mycophenolate Mofetil
ABSTRACT Pigmented oral lichen planus (OLP) is a chronic, immune‐mediated mucosal disorder associated with dark black or brown discoloration secondary to the excess melanin deposition. This medical condition is often accompanied by the typical white (reticular) or red (erosive) OLP features and is refractory to conventional therapy. We report a case of
Tania Biswas +5 more
wiley +1 more source
“Austrianov sindrom” pri zdravem 16-mesečnem dečku
V prispevku predstavljamo klinični primer 16-mesečnega dečka s pljučnico, meningitisom in endokarditisom. Iz hemokulture je bil izoliran Streptococcus pneumoniae tip 10A. Invazivna pnevmokokna okužba s triado pljučnica, meningitis in endokarditis je bila
Tina Weis +4 more
doaj +1 more source
Additional file 1: Table S1. Histopathological results for cases displaying arteritis/periarteritis (n=40) and cases of PFTS featuring periarteritis/arteritis (n=7), in total 47 cases.
Cobos, Àlex +5 more
openaire +1 more source
PCV chemotherapy for recurrent glioblastoma multiforme.
The authors evaluated response, time to progression (TTP), survival, prognostic factors, and toxicity in 63 patients with a recurrent glioblastoma multiforme treated with procarbazine, lomustine, and vincristine (PCV) chemotherapy.
Kappelle, AC +27 more
core +1 more source
ABSTRACT Ankylosing spondylitis (AS) is a chronic immune‐mediated inflammatory arthropathy primarily affecting the axial skeleton but may involve peripheral joints, particularly the hips. Avascular necrosis (AVN) of the femoral head represents a severe, underrecognized complication whose pathogenesis in AS is multifactorial—encompassing disease ...
Syeda Simrah Shah +5 more
wiley +1 more source
ABSTRACT Catastrophic antiphospholipid syndrome (CAPS) is a fulminant and rare variant of antiphospholipid syndrome characterized by rapidly progressive multiorgan thrombosis and a high mortality rate. Its diagnosis is often challenging due to overlapping clinical features with sepsis, thromboembolic disorders, and systemic autoimmune diseases.
Nazmin Ahmed +4 more
wiley +1 more source
ObjectiveTo analyze the clinical characteristics and pertussis-containing vaccine (PCV) vaccination status of 650 pertussis cases in Jiangning district, Nanjing city, Jiangsu province, to provide a reference for the development of pertussis vaccination ...
Yijun WANG +4 more
doaj +1 more source
Additional file 2: Table S2. Tissue availability per each studied case, including histological results and PCV-3 genome detection results (qPCR and ISH results).
Cobos, Àlex +5 more
openaire +1 more source
ABSTRACT Background Anemia remains highly prevalent among children aged 6–23 months in sub‐Saharan Africa. Previous estimates relied on outdated World Health Organization (WHO) hemoglobin cutoffs, which may have overestimated the burden. This study assessed anemia prevalence and associated factors using the updated 2024 WHO thresholds in nine sub ...
Temesgen Gebeyehu Wondmeneh
wiley +1 more source

