Results 161 to 170 of about 45,547 (280)
Objective The aim of this study was to develop and validate International Classification of Diseases (ICD) code–based algorithms for identifying systemic sclerosis (SSc) cases within electronic health record (EHR) data and to evaluate algorithm performance. Methods We identified patients with at least one ICD, Ninth Revision (ICD‐9)/ICD‐10 code for SSc
Gulsen Ozen +3 more
wiley +1 more source
Clinical features of dengue-associated myositis in children: a retrospective study. [PDF]
Birne RO +7 more
europepmc +1 more source
ABSTRACT We present the case of a 78‐year‐old woman with metabolic syndrome and a history of multiple ischemic strokes who developed progressive symmetrical proximal muscle weakness, predominantly affecting the lower extremities, while on atorvastatin.
Nischal Shrestha +2 more
wiley +1 more source
Orbital myositis last year and now Crohn's disease: A case report of a rare association. [PDF]
Patel A +4 more
europepmc +1 more source
Keywords: inclusion body myositis; sporadic inclusion body myositis (sIBM) - common myopathy in Caucasians over 50 years of age; epidemiology and genetic susceptibility; genetic susceptibility, linked to HLA-DR3 and 8.1 MHC ancestral haplotype (AH)
Mastaglia, F.L., Needham, M.
core
Abdominal Wall Desmoid Tumor Misdiagnosed as Schwannoma: A Case Report
ABSTRACT We present the case of a 35‐year‐old woman with an abdominal wall mass initially diagnosed radiologically as a schwannoma. Histopathology revealed desmoid fibromatosis through β‐catenin positivity, despite no trauma or surgical history. Complete excision with negative margins was curative, highlighting immunohistochemistry's diagnostic value ...
Faten Limaiem, Mohamed Hajri
wiley +1 more source
Comparative neurologic toxicity profiles of chemotherapy versus immune checkpoint inhibitors in melanoma: a propensity score-matched analysis. [PDF]
Abualrob MA +7 more
europepmc +1 more source
Mitochondrial DNA variants in inclusion body myositis
Mitochondrial DNA variants have been shown to be associated with many diseases. Mutations at mitochondrial DNA nucleotide positions 3192, 3196, 3397 and 4336 have been described in association with late-onset Alzheimer's disease.
Kok, C.C. +8 more
core
Muscular involvement in Sjögren's disease is associated with male gender, Ro52 autoantibodies, and a higher clinical activity. [PDF]
Gründges C +10 more
europepmc +1 more source

