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Toplam kayıt 14, listelenen: 1-10
Idiopathic focal organizing pneumonia mimicking malignancy
(African Field Epidemiology Network-Afenet, 2020)
Idiopathic FOP is a rare type of COP. What we know on this subject is made up of a few clinical cases published in recent years. Our patient was admitted to the hospital with an intermittent coughing complaint that worsens ...
Evaluation of the morphological and clinical features of left anterior descending myocardial bridging with multi-detector computed tomography
(Termedia Publishing House Ltd., 2021)
Aim: The aim of the study was to assess the incidence, localization, depth, length of myocardial bridging (MB) with left anterior descending (LAD), systolic compression ratio, atherosclerotic plaque localization and degree ...
The evaluation of unilateral closed-lip schizencephaly on complex MRI sequences
(Editura Medicala, 2021)
Schizencephaly is one of the rare cortical malformations that classify in the group of neurological migration defects. The appearance of the anomaly is in the form of a cleft that passes through the brain parenchyma. In ...
Osteochondroma as a cause of ischiofemoral impingement – first case series
(Vilnius University Press, 2021)
Ischiofemoral impingement (ISFI) is the compression of the quadratus femoris muscle resulting from the narrowed distance between the lesser trochanter and the ischial bone. Congenital factors (such as developmental hip ...
An Omitted Radiological finding in the Pediatric Age Group: Physiological Sacroiliac Joint Vacuum Normal Variant
(PMC, 2021)
Introduction: Gas accumulation in human joint spaces has been generally described as the vacuum phenomenon (VP). To date, the sacroiliac joint VP has been associated mostly with pathological, particularly degenerative ...
Diffusion Weighted Imaging and MR Spectroscopic Findings in Maple Syrup Urine Disease: The Importance of Early Radiological Diagnosis in the Prevention of Cerebral Parenchymal Damage
(MEDCOM LTD, 2021)
Maple Syrup Urine Disease is a very rare autosomal recessive inherited disease that results from the defect in the catalytic activity of the alpha ketoacid dehydrogenase enzyme complex. The deficiency in the catabolism of ...
The contribution of susceptibility-weighted imaging (SWI) in the central nervous system superficial siderosis’ evaluation in 3 Tesla magnetic resonance imaging (MRI)
(Editura Medicala, 2021)
Objective. The aim of this study is to evaluate the magnetic resonance imaging (MRI) findings of central neural system (CNS) superficial siderosis cases and the diagnostic contribution of the susceptibility-weighted imaging ...
Is Fat Deposition of Renal Sinus a Concomitant Finding to Fatty Liver Disease? The First Study Regarding the Relationship Between Kidney and Liver Fat Content with Non-Contrast Computed Tomography
(MSU College of Osteopathic Medicine Statewide Campus System, 2022)
Introduction: It has been established that abnormal fat deposits are associated with fat deposition in other abdominal regions and linked to obesity, diabetes mellitus, hypertension, vascular and metabolic diseases. This ...
The evaluation of cerebral venous normal anatomy and variations by phase-contrast cranial magnetic resonance venography
(Via Medica, 2021)
Background: The aim of our study is to determine the ability of the PC-CMRV technique to detect cranial anatomy, variations, thrombosis, to reveal the deficits of the technique and to discuss the reasons for these deficits ...
FIBRO DYSPLASIA OSSIFICANS PROGRESSIVA
(MedGen, 2022)
Letter to Editor