Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Ahmed A, Hawash"'
Autor:
Ghada Nour Eldeen, Tarek A. Elkhooly, Gehan T. El Bassyouni, Tamer M. Hamdy, Ahmed R. Hawash, Riham M. Aly
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-16 (2024)
Abstract Most of the conditions involving cartilaginous tissues are irreversible and involve degenerative processes. The aim of the present study was to fabricate a biocompatible fibrous and film scaffolds using electrospinning and casting techniques
Externí odkaz:
https://doaj.org/article/a04e934279494f53a7c18be87ac07a3a
Publikováno v:
Acta Dermato-Venereologica, Vol 101, Iss 10 (2021)
Keloids are scars that extend beyond the margins of an insulting cutaneous injury. Keloids are often thought to be primarily a cosmetic issue, as they are typically quite raised and pigmented. However, these scars also present with functional symptom
Externí odkaz:
https://doaj.org/article/7036c22fc013493fac3992182129a197
Autor:
Jessica H Myers, Kirsten Denman, Chris DuPont, Ahmed A Hawash, Kevin R Novak, Andrew Koesters, Manfred Grabner, Anamika Dayal, Andrew A Voss, Mark M Rich
Publikováno v:
eLife, Vol 10 (2021)
In addition to the hallmark muscle stiffness, patients with recessive myotonia congenita (Becker disease) experience debilitating bouts of transient weakness that remain poorly understood despite years of study. We performed intracellular recordings
Externí odkaz:
https://doaj.org/article/f201e13c4e5f4c20b08b45b730d90c95
Publikováno v:
Experimental Dermatology. 30:1208-1217
While there is a vast array of aetiologies that may lead to chronic pruritus, recent data suggests that many of these conditions share similar interactions between keratinocytes, nerves, and the immune system. Specifically, the type 2 immune response
Publikováno v:
Dermatologic Therapy. 35
Publikováno v:
Exp Neurol
Patients with myotonia congenita suffer from muscle stiffness caused by muscle hyperexcitability. Although loss-of-function mutations in the ClC-1 muscle chloride channel have been known for 25 years to cause myotonia congenita, this discovery has le
Autor:
Kevin R. Novak, Anamika Dayal, Chris DuPont, Jessica H Myers, Mark M. Rich, Andrew Koesters, Kirsten Denman, Andrew A. Voss, Manfred Grabner, Ahmed A. Hawash
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f6215c5c397370bb10183025c7f0aad
https://doi.org/10.7554/elife.65691.sa2
https://doi.org/10.7554/elife.65691.sa2
Autor:
Chris DuPont, Anamika Dayal, Andrew Koesters, Kevin R. Novak, Kirsten Denman, Andrew A. Voss, Jessica H Myers, Ahmed A. Hawash, Mark M. Rich, Manfred Grabner
Publikováno v:
eLife, Vol 10 (2021)
eLife
eLife
In addition to the hallmark muscle stiffness, patients with recessive myotonia congenita (Becker disease) experience debilitating bouts of transient weakness that remain poorly understood despite years of study. We performed intracellular recordings
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93b40765fcf9a44c20c5417a622d7891
https://doi.org/10.1101/2020.12.23.424129
https://doi.org/10.1101/2020.12.23.424129
Autor:
W. David Arnold, John T. Kissel, Julie Agriesti, Amy Bartlett, Mark M. Rich, David Kline, Ahmed A. Hawash, Miriam Freimer, Samantha LoRusso
Publikováno v:
Muscle & Nerve. 59:240-243
Introduction Paramyotonia congenita (PMC) is a nondystrophic myotonic disorder that is believed to be caused by a defect in Nav 1.4 sodium channel inactivation. Ranolazine, which acts by enhancing slow inactivation of sodium channels, has been propos
Publikováno v:
JAAD Case Reports
Inhalant abuse is the intentional inhalation of volatile substances to achieve intoxication. Inhaled substances include cheap, easily accessible, legal, everyday products, and abuse is most common in adolescence. There is considerable morbidity and m