Results 191 to 200 of about 72,988 (243)
ABSTRACT Groin swellings are the most frequent presenting clinical signs, which most frequently arise due to an inguinal hernia or lymphadenopathy. There are also rare congenital lesions, such as dermoid cysts, which can present similarly to common lesions, also leading to a diagnostic challenge.
Muhammad Hassaan Javaid +3 more
wiley +1 more source
Commentary: Grading of clear cell renal cell carcinoma using diffusion MRI with a multimodal apparent diffusion model. [PDF]
Chen J, Huang P, Yang L.
europepmc +1 more source
ABSTRACT Introduction Primary malignant neoplasms of the epididymis are rare. In this case report, we describe clear cell carcinoma associated with papillary cystadenoma of the epididymis (PCE). Case Presentation A 77‐year‐old man presented with a painless, enlarged left scrotum.
Hiroko Suzuki +9 more
wiley +1 more source
Both transient ischaemic attack (TIA) and ischaemic stroke lead to an increase in individual cellular‐derived populations of extracellular vesicles (EVs), including endothelial, platelet and leukocyte derived. These EVs have downstream roles in the pathophysiological events associated with TIA and stroke, including dysregulated inflammation and ...
Rebecca Marie Raven +3 more
wiley +1 more source
ABSTRACT COASY protein associated neurodegeneration is a rare, progressive autosomal recessive neuroferritinopathy due to pathogenic mutations in the COASY gene, coding for the mitochondrial located coenzyme A synthase. Clinical manifestations include seizures, progressive spasticity, dystonia, neuropathy, cognitive decline and neuropsychiatric ...
Matthew Lynch +8 more
wiley +1 more source
The diagnostic performance of ss-EPI-DWI, rs-EPI-DWI (RESOLVE) and TGSE-BLADE-DWI in a model of retinal ischemia: a comparative phantom study. [PDF]
Schütze A +5 more
europepmc +1 more source
Metabolic Stroke: Atypical Presentation of Succinic Semialdehyde Dehydrogenase Deficiency
ABSTRACT Succinic semialdehyde dehydrogenase (SSADH) deficiency is a rare autosomal recessive neurometabolic disorder caused by biallelic pathogenic variants in ALDH5A1, encoding the mitochondrial enzyme SSADH. This enzyme catalyses the conversion of succinic semialdehyde to succinic acid in the γ‐aminobutyric acid (GABA) degradation pathway.
Sharmila Kiss +10 more
wiley +1 more source
Comparison of image quality between simultaneous multi-slice single-shot EPI and readout-segmented EPI in diffusion-weighted imaging of prostate cancer: a retrospective study. [PDF]
Zhang T, Chen J, Li M, Shen A.
europepmc +1 more source
A DWI histogram-based nomogram for preoperative prediction of pathogens and antibiotic resistance in perianal abscesses. [PDF]
Wang J +8 more
europepmc +1 more source

