Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Bandar Al-Ghamdi"'
Autor:
Bandar Al-Ghamdi, Fahmi A Alkaf, Menwar M Al-Anazi, Yahya Al Hebaishi, Normeen A Al Othimeen, Asirvatham Alwin Robert, Osman Ahmed, Abdullah Alkhushail
Publikováno v:
SAGE Open Medical Case Reports, Vol 8 (2020)
Nonbacterial thrombotic endocarditis, a form of noninfectious thrombotic endocarditis, is mainly characterized by deposition of sterile platelet thrombi on heart valves. Usually, it is observed in advanced malignancy. Herein, we report a case of a pr
Externí odkaz:
https://doaj.org/article/e9125cf1f792450eab053c0907ccfe0d
Publikováno v:
HeartRhythm Case Reports, Vol 3, Iss 4, Pp 229-232 (2017)
Externí odkaz:
https://doaj.org/article/54f93c3849b44b4cb5cd11f0efdc0573
Autor:
Ahmed L. Fathala, Salwa Q. Bukhari, Mohamed Shoukri, Hani El Sergani, Bandar Al-Ghamdi, Abdulaziz Al-Sugair
Publikováno v:
Annals of Saudi Medicine, Vol 37, Iss 2, Pp 154-160 (2017)
BACKGROUND: Normal single-photon emission computed tomography (SPECT) myocardial perfusion imaging (MPI) has a high negative predictive value for ischemic heart disease. Thus, the presence of subclinical coronary atherosclerosis detected by coronary
Externí odkaz:
https://doaj.org/article/d390013d289e48729dceb372442ddfdc
Autor:
Bandar Al-Ghamdi
Publikováno v:
Case Reports in Cardiology, Vol 2019 (2019)
Patients with complex congenital heart disease (CHD) and low left ventricular ejection fraction are at an increased risk of sudden cardiac death (SCD). Prevention of SCD by subcutaneous implantable cardioverter defibrillator (S-ICD) implantation may
Externí odkaz:
https://doaj.org/article/212286ddfe4743b29884ea100b3b381b
Autor:
Nawal Salahuddin, Azam Shafquat, Qussay Marashly, Khaled Juan Zaza, Moh’d Sharshir, Moazzum Khurshid, Zeeshan Ali, Melissa Malgapo, Mouhamad Ghyath Jamil, Mohamed Shoukri, Mohammed Hijazi, Bandar Al-Ghamdi
Publikováno v:
Cardiology Research and Practice, Vol 2018 (2018)
Background. Reduced heart rate variability (HRV) indicates dominance of the sympathetic system and a state of “physiologic stress.” We postulated that, in patients with critical illness, increases in HRV might signal successful resuscitation and
Externí odkaz:
https://doaj.org/article/de82090249984b518f8bc3b297c3caab
Publikováno v:
Annals of Saudi Medicine, Vol 34, Iss 5, Pp 415-426 (2014)
BACKGROUND AND OBJECTIVES: Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a rare genetic disorder that primarily involves the right ventricle (RV). It is characterized by progressive replacement of RV myocardium by fibrofatty t
Externí odkaz:
https://doaj.org/article/0b8bd890c9ad461981f1b6d2de630131
Autor:
Abdurahman Jamiel, Mohammed Hashim, Antonio Sorgente, Bandar Al Ghamdi, Amjad Al-Mandalawi, Raed Sweidan, Ahmad Hersi, Haitham Alanazi, Edmon Benjamin Khammo, Ismail Al Abri, Mohammad Mehdi Amin, Mohamed ElMaghawry, Abdulmohsen Almusaad, Nima Badie, Najib Alrawahi, Maria Luisa Loricchio, Alexandre Chami, Ahmed Al Fagih, Ghaliah Al Mohanny, Yahya Alhebaishi, Nazar Sudan, Fayez Bokhari, Naeem A. Alshoaibi, Mohamed Sayed
Publikováno v:
Journal of Interventional Cardiac Electrophysiology. 63:399-407
Purpose Cardiac resynchronization therapy (CRT) with multipoint left ventricular (LV) pacing (MultiPoint™ Pacing, MPP) has been shown to improve CRT response, although MPP response using automated pacing vector programming has not been demonstrated
Publikováno v:
Drug Metabolism and Personalized Therapy.
Objectives Despite its wide usage, warfarin therapy remains challenging due to its narrow therapeutic index, inter-individual response variability, and risk of bleeding. Previous reports have suggested that polymorphisms in VKORC1 and CYP2C9 genes co
Publikováno v:
Drug metabolism and personalized therapyReferences.
Despite its wide usage, warfarin therapy remains challenging due to its narrow therapeutic index, inter-individual response variability, and risk of bleeding. Previous reports have suggested that polymorphisms inThis cross-sectional study was conduct
Autor:
Abdullah S. Al-Kharashi, Ahmed M. Abu El-Asrar, Emad B. Abboud, Bandar Alamro, Fowzan S. Alkuraya, Ramadan Alturki, Rana Helaby, Niema Ibrahim, Bandar Al Ghamdi, Hisham Alkuraya, Nisha Patel, Mohammed D. Alotaibi, Sawsan R. Nowilaty, Abdulrahman Al-Hussaini, Sulaiman M. Alsulaiman, Amani Elshaer, Zainab Almasseri, Hamad Al-Zaidan, Naif A.M. Almontashiri, Wafaa Eyaid
Publikováno v:
Clinical Genetics. 97:447-456
Retinal arterial macroaneurysms with supravalvular pulmonic stenosis (RAMSVPS), also known as Familial Retinal Arterial Macroaneurysms (FRAM) syndrome, is a very rare multisystem disorder. Here, we present a case series comprising ophthalmologic and