Heart failure with reduced ejection fraction and chronic kidney disease: a focus on therapies and interventions.

Autor: Taha HSE; Cardiology Department, Kasr Al-Ainy Faculty of Medicine, Cairo University, Giza, Egypt., Momtaz M; Nephrology & Internal Medicine, Internal Medicine Department, Kasr Al-Ainy Faculty of Medicine, Cairo University, Giza, Egypt., Elamragy AA; Cardiology Department, Kasr Al-Ainy Faculty of Medicine, Cairo University, Giza, Egypt., Younis O; Cardiology Department, National Heart Institute, 5 Ibn Al Nafees Square, Al Kit Kat, Giza, 12651, Egypt. dr.omar_younis@outlook.com., Fahim MAS; Cardiology Department, Kasr Al-Ainy Faculty of Medicine, Cairo University, Giza, Egypt.

Publikováno v: Heart failure reviews [Heart Fail Rev] 2025 Jan; Vol. 30 (1), pp. 159-175. Date of Electronic Publication: 2024 Oct 18.

Personal and public safety issues related to arrhythmias that may affect consciousness: implications for regulation and physician recommendations. A medical/scientific statement from the American Heart Association and the North American Society of Pacing and Electrophysiology

Autor: Levine Pa, Wilkoff Bl, A. E. Epstein, Friedman Pl, Harvey Jc, A. Garson, A. J. Camm, Kidwell Ga, Francis E. Marchlinski, E. N. Prystowsky, Klein Gj, David G. Benditt, Miles Wm, Darling Ej

Publikováno v: Circulation. 94(5)

Patients with arrhythmias may experience complete or partial loss of consciousness, and questions about activities that are safe for them arise every day. Probably the most common question concerns the advisability of driving, because the safety of b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b65491cf8bdc4f4f259c49de303f2c1
https://pubmed.ncbi.nlm.nih.gov/17287391

Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

Autor: Faridi R; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.; National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan., Rehman AU; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA., Morell RJ; Genomics and Computational Biology Core, NIDCD, NIH, Bethesda, MD, USA., Friedman PL; Internal Medicine Consult Service, Clinical Center, National Institutes of Health, Bethesda, MD, USA., Demain L; Manchester Centre for Genomic Medicine, University of Manchester and Central Manchester University Hospitals, NHS Foundation Trust, Manchester, UK., Zahra S; National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan., Khan AA; National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan., Tohlob D; Manchester Centre for Genomic Medicine, University of Manchester and Central Manchester University Hospitals, NHS Foundation Trust, Manchester, UK.; Clinical Pathology Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt., Assir MZ; Allama Iqbal Medical College, University of Health Sciences, Lahore, Pakistan.; Shaheed Zulfiqar Ali Bhutto Medical University, Pakistan, Institute of Medical Sciences, Islamabad, Pakistan., Beaman G; Manchester Centre for Genomic Medicine, University of Manchester and Central Manchester University Hospitals, NHS Foundation Trust, Manchester, UK., Khan SN; National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan., Newman WG; Manchester Centre for Genomic Medicine, University of Manchester and Central Manchester University Hospitals, NHS Foundation Trust, Manchester, UK., Riazuddin S; Shaheed Zulfiqar Ali Bhutto Medical University, Pakistan, Institute of Medical Sciences, Islamabad, Pakistan.; Allama Iqbal Medical Research Centre, Jinnah Hospital Complex, Lahore, Pakistan., Friedman TB; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, USA.

Publikováno v: Clinical genetics [Clin Genet] 2017 Feb; Vol. 91 (2), pp. 328-332. Date of Electronic Publication: 2016 Nov 16.

Successful management of massive digoxin overdose using DIGIFab and therapeutic plasma exchange: a case report.

Autor: Alhussein, Reema M.¹ (AUTHOR) Reemaalhusseinn@gmail.com, Alamri, Nawaf A.¹ (AUTHOR), Alhashem, Hussain M.¹ (AUTHOR), Alarifi, Mohammed I.² (AUTHOR), Alyahya, Bader³ (AUTHOR)

Publikováno v: Journal of Medical Case Reports. 3/5/2024, Vol. 18 Issue 1, p1-6. 6p.

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