Results 261 to 270 of about 36,061 (316)

Antenatal predictors of intestinal pathologies in fetal bowel dilatation

Journal of Paediatrics and Child Health, 2020
AimFetal bowel dilatation (FBD) in the late trimester of pregnancy can be related with varies of prognosis. Our aims were to obtain antenatal factors that might have relevance for the distinct prognosis with FBD.MethodsSeven features of 68 pregnancies presented with FBD were assessed.
Lan Huang, Danping Huang, Hongying Wang, Xiangxiang Zhang, Hongkui Yu, Pan Yang   +5 more
openaire   +2 more sources

Pathological analysis of hypertrophic cardiomyopathy simulating dilated cardiomyopathy

Acta Pathologica Japonica, 1993
The pathomorphologic features of hypertrophic cardiomyopathy simulating dilated cardiomyopathy in the late stage (HCM‐DCM) were compared with those of ordinary hypertrophic cardiomyopathy (HCM). Seven autopsied hearts with HCM‐DCM and 11 with HCM were assessed quantitatively using an image analyzer.
T, Kawashima, Y, Yokota, M, Yokoyama, H, Itoh   +3 more
openaire   +2 more sources

Discrimination between physiologic and pathologic left ventricular dilatation

International Journal of Cardiology, 2006
The identification of certain cardiovascular disease in athletes may constitute the basis for disqualification from competition in an effort to minimize the risk of sudden cardiac death. The aim of this study was to assess diastolic and systolic parameters measured by tissue Doppler imaging in endurance veteran athletes who had prominent cardiac ...
Hulya Akhan, Kasikcioglu, Erdem, Kasikcioglu, Huseyin, Oflaz, Sennur, Unal, Berrin, Topcu, Zeynep, Tartan, Armagan, Arslan, Nese, Cam, Abidin, Kayserilioglu   +8 more
openaire   +2 more sources

Clinical and pathologic study of familial dilated cardiomyopathy

The American Journal of Cardiology, 1990
To evaluate the occurrence of familial cases of dilated cardiomyopathy (DC), 165 consecutive patients were studied. Diagnosis of myocardial disease was based on clinical, hemodynamic, bioptic, postmortem or a combination of these criteria. Twelve patients (7% of cases) showed evidence of myocardial disease in greater than or equal to 1 relative; 27 ...
MESTRONI L, MIANI D, DI LENARDA A, SILVESTRI, FURIO, BUSSANI, ROSSANA, FILIPPI G, CAMERINI F.   +6 more
openaire   +3 more sources

Pathologic Changes of the Trachea After Percutaneous Dilational Tracheostomy

Chest, 1996
The tracheas of 12 patients who had undergone autopsies after percutaneous dilatational tracheotomy (PDT) were analyzed macroscopically and microscopically. The puncture site of the trachea varied from just below the cricoid cartilage (two patients) to below the third ring (three patients).
L W, van Heurn, P H, Theunissen, G, Ramsay, P R, Brink   +3 more
openaire   +2 more sources

Pathologic anatomy of the dilated cardiomyopathies

The American Journal of Cardiology, 1989
Dilated cardiomyopathies are characterized by systolic pump failure and by dilatation of the ventricular cavity. Thus, they differ from the other 2 main types of cardiomyopathies, namely, hypertrophic cardiomyopathy and restrictive/obliterative cardiomyopathy.
openaire   +2 more sources

Allograft Pathology in Patients Transplanted for Idiopathic Dilated Cardiomyopathy

American Journal of Surgical Pathology, 2012
There are few morphologic studies on idiopathic dilated cardiomyopathy (CM) treated with transplant. We prospectively correlated gross, histologic, and clinical findings pertaining to hearts explanted in a 5-year period from patients with a clinical diagnosis of nonischemic CM and also correlated left ventricular diameter with preoperative ...
Mingchang, Zhang, Fabio, Tavora, Thomas, Huebner, Jonathan, Heath, Allen, Burke   +4 more
openaire   +2 more sources

Phenotype and pathology of the dilated cardiomyopathy with ataxia syndrome in children

Journal of Inherited Metabolic Disease, 2021
AbstractThe dilated cardiomyopathy with ataxia syndrome (DCMA) is an autosomal recessive mitochondrial disease caused by mutations in the DnaJ heat shock protein family (Hsp40) member C19 (DNAJC19) gene. DCMA or 3‐methylglutaconic aciduria type V is globally rare, but the largest number of patients in the world is found in the Hutterite population of ...
Pranav Machiraju, Vlad Degtiarev, Dhwani Patel, Hassan Hazari, R. Brian Lowry, Tanya Bedard, David Sinasac, Marie‐Anne Brundler, Steven C. Greenway, Aneal Khan   +9 more
openaire   +2 more sources

Tracheal lesion caused by percutaneous dilatational tracheostomy - a clinico-pathological study

Intensive Care Medicine, 1999
To analyse the accuracy of cannula placement and the extent of tracheal lesions of the anterior tracheal wall after percutaneous dilatational tracheostomy (PDT).A clinico-pathological study of tracheal specimens following PDT.University hospital.Forty-two tracheal specimens of intensive care patients (24 male, 18 female; age: 23-70 years) who died ...
M K, Walz, U, Schmidt
openaire   +2 more sources

Hepatic Sinusoidal Dilatation: A Review of Causes With Imaging-Pathologic Correlation

Seminars in Ultrasound, CT and MRI, 2016
Hepatic sinusoids are vascular conduits connecting the portal triad with the central vein. Multiple conditions can lead to sinusoidal dilatation and congestion with resultant stasis of blood within the lumen. The altered hemodynamics associated with hepatic sinusoidal dilatation generally result in heterogeneous enhancement of the hepatic parenchyma on
Furlan, A., Minervini, M., Borhani, A., Dioguardi Burgio, M., Tublin, M., BRANCATELLI, Giuseppe   +5 more
openaire   +2 more sources