Results 1 to 10 of about 71,653 (158)

Exaggerated Placental Site Reaction: A Challenging Diagnosis [PDF]

Case Reports in Obstetrics and Gynecology
Gestational trophoblastic disease (GTD) includes both neoplastic and nonneoplastic disorders arising from placental trophoblastic tissue. Among tumor-like conditions, exaggerated placental site reaction (EPSR) is a rare benign condition characterized by ...
Eleonora Nardi, Silvio Tartaglia, Davide Mulone, Ursula Catena, Antonio Lanzone, Vincenzo Arena   +5 more
doaj   +2 more sources

Mechanism behind the recombination requirement for benign termination of relativistic electron beams

Nuclear Fusion
We present a first-principles explanation of the recombination requirement for benign termination of relativistic electron (RE) beams in tokamaks. Kinetic modeling including neutrals shows that a specific range in injected neutral quantity results in ...
G. Su, C.F.B. Zimmermann, C. Paz-Soldan, M. Hölzl, P. Aleynikov   +4 more
doaj   +3 more sources

Plasma exchange-based artificial liver support for acute liver failure associated with early-onset intrahepatic cholestasis of pregnancy: a case report [PDF]

BMC Pregnancy and Childbirth
Background Intrahepatic cholestasis of pregnancy (ICP) is typically benign, but progression to acute liver failure (ALF) is a rare, life-threatening complication.
Yannan Zhu, Zuoxin Qin, Haiyan Tang, Bangmin Li   +3 more
doaj   +2 more sources

Prevalence and characteristics of coronary anomalies in Bulgarian patients undergoing coronary angiography [PDF]

BMC Cardiovascular Disorders
Background Coronary artery anomalies (CAAs) are rare congenital abnormalities with variable reported prevalence. Data from Eastern Europe remain limited.
Rozen Grigorov, Stefan Yambolov, Ivaylo Borisov, Nikolai Nikolov, Svetoslav Georgiev   +4 more
doaj   +2 more sources

Clinical and genetic analysis of PRRT2 gene mutations in a cohort of 21 pediatric patients: a case series [PDF]

Frontiers in Pediatrics
BackgroundThe Proline-Rich Transmembrane Protein 2 (PRRT2) gene is associated with a spectrum of autosomal dominant paroxysmal disorders, including Benign Familial Infantile Epilepsy (BFIE), Paroxysmal Kinesigenic Dyskinesia (PKD), and Hemiplegic ...
Xiaolan Zheng, Caimei Lin
doaj   +2 more sources

Benign termination of runaway electron beams on ASDEX Upgrade and TCV

Plasma Physics and Controlled Fusion
Abstract This paper discusses the development of a benign termination scenario for runaway electron (RE) beams on ASDEX Upgrade and TCV. A systematic study revealed that a low electron density (n e) companion plasma was required to achieve a large MHD instability, which expelled the confined REs over a large wetted area
Sheikh, U., Decker, J., Hoppe, M., Pedrini, M., Sieglin, B., Simons, L., Cazabonne, J.A., Caloud, J., Cerovsky, J., Wijkamp, T., Coda, S., Colandrea, C., Dal Molin, A., Duval, B., Ficker, O., Griener, M., Papp, G., Pautasso, G., Paz-Soldan, C., Reux, C., Tomesova, E., Team, ASDEXUpgrade, TCV team,, Team, MST1   +23 more
exaly   +8 more sources

Variability of MHD instabilities in benign termination of high-current runaway electron beams in the JET and DIII-D tokamaks

Nuclear Fusion
Benign termination, in which magnetohydrodynamic (MHD) instabilities deconfine runaway electrons (REs) following hydrogenic injections, is a promising strategy for mitigating dangerous RE loads after disruptions.
C.F.B. Zimmermann, C. Paz-Soldan, G. Su, C. Reux, A.F. Battey, O. Ficker, S.N. Gerasimov, C.J. Hansen, S. Jachmich, A. Lvovskiy, J. Puchmayr, N. Schoonheere, U. Sheikh, I.G. Stewart, G. Szepesi, JET Contributors, the EUROfusion Tokamak Exploitation Team   +16 more
doaj   +4 more sources

Wilson disease associated with a novel variant in the ATP7B gene [PDF]

Frontiers in Neurology
IntroductionWilson disease is an autosomal recessive monogenic disorder caused by mutations in the copper-transporting P-type ATPase beta gene (ATP7B) located on human chromosome 13. This gene encodes copper-transporting P-type ATPase.
Lipeng Yang, Jun Li, Si Xie, Xinhong Feng   +3 more
doaj   +2 more sources

Carotid Sinus Syndrome Secondary to Laryngocele: A Case Report [PDF]

Iranian Journal of Otorhinolaryngology, 2021
Introduction: Carotid sinus syndrome (CSS) is a hypersensitivity of the carotid sinus manifested by atrioventricular sinus bradycardia or decreased arterial pressure of at least 50 mmHg.
Enzo Chianetta, Barbara Verro, Giuseppe Greco, Rosalia Gargano   +3 more
doaj   +1 more source

Benign but Terminal: Cardiopulmonary Collapse from a Massive Chest Wall Lipoma [PDF]

Journal of Investigative Medicine High Impact Case Reports, 2020
Lipomas are the most common benign soft tissue tumor. Yet, strikingly simple tumors can become problematic when compounded by odd characteristics such as size and location. We report the case of a 53-year-old male who developed complete right lung collapse secondary to a large right-sided chest wall lipoma with accelerated growth in the past 6 months ...
Shweta Paulraj, Prateek Suresh Harne, Kanish Mirchia, Sundus Mian, Raman Sohal, Gaston Habib, Amish Shah, Ioana Amzuta   +7 more
openaire   +3 more sources