Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Ana P. Abdala"'
Publikováno v:
Physiological Reports, Vol 10, Iss 19, Pp n/a-n/a (2022)
Abstract Rett Syndrome (RTT) is a congenital, X‐chromosome‐linked developmental disorder characterized by developmental delay, dysautonomia, and breathing irregularities. RTT is also associated with sudden death and QT intervals are prolonged in
Externí odkaz:
https://doaj.org/article/f05ecb1cad914724ab07bd42c5bb7a28
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 10, p 5735 (2022)
Rett syndrome (RTT) is a severe developmental disorder that is strongly linked to mutations in the MECP2 gene. RTT has been associated with sudden unexplained death and ECG QT interval prolongation. There are mixed reports regarding QT prolongation i
Externí odkaz:
https://doaj.org/article/b91fbb8a24ab469b9373cd0a8e2a006c
Autor:
Krzysztof Narkiewicz, MD, Laura E.K. Ratcliffe, BSc, MBBS, Emma C. Hart, PhD, Linford J.B. Briant, PhD, Marzena Chrostowska, PhD, Jacek Wolf, MD, Anna Szyndler, MD, Dagmara Hering, MD, Ana P. Abdala, PhD, Nathan Manghat, MD, Amy E. Burchell, MA, BMBCh, Claire Durant, PhD, Melvin D. Lobo, Paul A. Sobotka, MD, Nikunj K. Patel, MBBS, MD, James C. Leiter, MD, Zoar J. Engelman, PhD, Angus K. Nightingale, MB, BChir, MD, Julian F.R. Paton, PhD
Publikováno v:
JACC: Basic to Translational Science, Vol 1, Iss 5, Pp 313-324 (2016)
Animal and human data indicate pathological afferent signaling emanating from the carotid body that drives sympathetically mediated elevations in blood pressure in conditions of hypertension. This first-in-man, proof-of-principle study tested the saf
Externí odkaz:
https://doaj.org/article/090de4c0ffaa48999a72a1b604d2cccd
Autor:
Ahmed El-Medany, Zoe H. Adams, Hazel C. Blythe, Katrina A. Hope, Adrian H. Kendrick, Ana Paula Abdala Sheikh, Julian F. R. Paton, Angus K. Nightingale, Emma C. Hart
Publikováno v:
Communications Medicine, Vol 4, Iss 1, Pp 1-10 (2024)
Abstract Background The symptoms of long COVID, which include fatigue, breathlessness, dysregulated breathing, and exercise intolerance, have unknown mechanisms. These symptoms are also observed in heart failure and are partially driven by increased
Externí odkaz:
https://doaj.org/article/236c1c97f455485b8a53adfd42f438cb
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2023)
Introduction: Deaths due to overdose of fentanyls result primarily from depression of respiration. These potent opioids can also produce muscle rigidity in the diaphragm and the chest muscles, a phenomenon known as Wooden Chest Syndrome, which furthe
Externí odkaz:
https://doaj.org/article/194f6592d1d24af48639a4667c1637a4
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-5 (2018)
Abstract The reversal of the Rett syndrome disease process in the Mecp2 mouse model of Guy et al. (2007) has motivated families and researchers to work on this condition. The reversibility in adult mice suggests that there is potentially much to be g
Externí odkaz:
https://doaj.org/article/e314279404264ecf95d272580b8e0976
Publikováno v:
Physiological Reports. 10
Publikováno v:
Physiological reports. 10(19)
Rett Syndrome (RTT) is a congenital, X-chromosome-linked developmental disorder characterized by developmental delay, dysautonomia, and breathing irregularities. RTT is also associated with sudden death and QT intervals are prolonged in some RTT pati