Results 51 to 60 of about 225,755 (317)
Türk Kardiyoloji Derneği Arşivi, 2013 Several studies have determined an association between obesity and increased risk of cardiac arrhythmia. Currently, due to the increased frequency of obesity, food-, plant-, and drug-based therapies for weight loss have gained great attention.
Hakkı Şimşek +3 more
doaj +1 more source
, 2020 Introduction:Supraventricular tachycardia is the most common cause of arrhythmia in children. The aim of this study was to determine the dose and efficacy of adenosine treatment in the management of supraventricular tachycardia and to determine the ...
Yüksel Bıcılıoğlu +5 more
core +1 more source
Pathogenic PF4/Polyanion ELISA‐Negative Antibodies in HIT
American Journal of Hematology, EarlyView.ABSTRACT Background Platelet factor 4‐polyanion enzyme‐linked immunosorbent assays (ELISAs) are considered highly sensitive for diagnosing heparin‐induced thrombocytopenia (HIT), such that current practice guidelines recommend use of ELISA‐negative results to exclude HIT.
Adam J. Kanack +25 more
wiley +1 more source
Right ventricular outflow tract tachycardia after an initial dose of amantadine
Türk Kardiyoloji Derneği Arşivi, 2015 Amantadine hydrochloride is an antiviral agent that is also effective in the treatment of Parkinson's disease. In the literature, cardiac arrhythmia is reported in toxic doses of amantadine, but in this paper we report a patient with right ventricular ...
Cüneyt Kocaş +3 more
doaj +1 more source
Journal of Pediatric Emergency and Intensive Care Medicine, 2023 The most common tachyarrhythmias in childhood are narrow QRS complex tachyarrhythmias. The majority of these are supraventricular tachycardia (SVT).
Aziz Zeytin, Çapan Konca, Celal Varan
doaj +1 more source
, 2005 Studies analyzing the diagnostic value of 12-lead electrocardiographic criteria differentiating slow-fast atrioventricular nodal reentrant tachycardia (AVNRT) from atrioventricular reentrant tachycardia (AVRT) due to concealed accessory pathway have ...
Dorszewski, Anja +8 more
core +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Griscelli Syndrome Type 2 (GS2) is a rare autosomal recessive disorder caused by pathogenic mutations in the RAB27A gene. Typically, it is characterized by cutaneous hypopigmentation, immunodeficiency, with or without neurological abnormalities secondary to hemophagocytic lymphohistiocytosis (HLH). Without treatment, GS2 often results in fatal
Dzhoy Papingi +6 more
wiley +1 more source
Diagnosis, Treatment and Follow-up of Fetal Cardiac Arrhythmia
Journal of Pediatric Research, 2021 Aim:The importance of managing fetal arrhythmia has increased with advances in fetal echocardiography. We aimed to describe the incidence, types, clinical characteristics, treatments, and follow-ups of patients diagnosed with fetal arrhythmia in our ...
Ayşe Şimşek, Tülay Demircan
doaj +1 more source
JAMA: The Journal of the American Medical Association, 1898 Mrs. —, aged 40, has many times during the last ten years told me about attacks of palpitation which she has had and which have come on suddenly, lasted from a few seconds to ten minutes and then as suddenly stopped. Many times I have been sent for when she had been having the attacks, but the heart would have quieted before I reached her.
openaire +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Autosomal recessive loss‐of‐function variants in PPP1R13L cause an ultra‐rare cardiocutaneous syndrome characterized by rapidly progressive arrhythmogenic cardiomyopathy (ACM). PPP1R13L encodes iASPP, which has two potentially overlapping mechanisms driving ACM as both a regulator of NFκB‐mediated inflammation and a binding partner within the ...
Aaron Renberg +9 more
wiley +1 more source