Zobrazeno 1 - 10
of 2 132
pro vyhledávání: '"G, Engel"'
Autor:
Xin‐Ming Shen, Tomohiko Nakata, Seiji Mizuno, Issei Imoto, Duygu Selcen, Kinji Ohno, Andrew G. Engel
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 5, Pp 732-743 (2023)
Abstract Objective To dissect the kinetic defects of acetylcholine receptor (AChR) γ subunit variant in an incomplete form of the Escobar syndrome without pterygium and compare it with those of a variant of corresponding residue in the AChR ε subun
Externí odkaz:
https://doaj.org/article/12fb62f583b14adf8b8977384aad2bd7
Autor:
Mark J. Stoltenberg, Maura Kennedy, Janet Rico, Matthew Russell, Laura A. Petrillo, Kirsten G. Engel, Mihir Kamdar, Kei Ouchi, David H. Wang, Rachelle H. Bernacki, Kevin Biese, Emily Aaronson
Publikováno v:
Journal of the American College of Emergency Physicians Open, Vol 3, Iss 6, Pp n/a-n/a (2022)
Abstract With the aging of our population, older adults are living longer with multiple chronic conditions, frailty, and life‐limiting illnesses, which creates specific challenges for emergency departments (EDs). Older adults and those with serious
Externí odkaz:
https://doaj.org/article/8fcf4daad6b348fbbdededa8ffbf4416
Autor:
Andrew G. Engel
Myasthenia Gravis and Myasthenic Disorders, Second Edition is a thoroughly re-written and updated version of the highly successful first edition published in 1999. The current edition begins with an overview of the anatomy and molecular architecture
Autor:
Xin‐Ming Shen, Margherita Milone, Hang‐Long Wang, Brenda Banwell, Duygu Selcen, Steven M. Sine, Andrew G. Engel
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 10, Pp 2066-2078 (2019)
Abstract Objective To characterize the molecular and phenotypic basis of a severe slow‐channel congenital myasthenic syndrome (SCCMS). Methods Intracellular and single‐channel recordings from patient endplates; alpha‐bungarotoxin binding studie
Externí odkaz:
https://doaj.org/article/d00ccbda480a4d6988125db4b30dce44
Publikováno v:
BMC Geriatrics, Vol 19, Iss 1, Pp 1-8 (2019)
Abstract Background Health-related quality of life (HRQoL), encompassing social, emotional, and physical wellbeing is an important clinical outcome of medical care, especially among geriatric patients. It is unclear which domains of HRQoL are most im
Externí odkaz:
https://doaj.org/article/e5b45db77d42450fa3ca6269dac4cbf1
Publikováno v:
Surgery for Obesity and Related Diseases. 19:344-349
While bariatric surgery results in substantial weight loss, one negative side effect of surgery is that patients often experience more rapid and intense intoxication effects after consuming alcohol.Given that alcohol use has been associated with impa
Autor:
Betina Ristorp Andersen, Maria Birkvad Rasmussen, Karl Bang Christensen, Kirsten G Engel, Charlotte Ringsted, Ellen Løkkegaard, Martin G Tolsgaard
Publikováno v:
PLoS ONE, Vol 15, Iss 2, p e0227988 (2020)
OBJECTIVE:This study aimed to identify factors influencing mothers' and their partners' perceptions of care quality, and to identify associated clinical factors. METHODS:Questionnaires were developed based on eight interviews with couples after emerg
Externí odkaz:
https://doaj.org/article/85473966984749cb8c46677c9afe8317
Autor:
Rachel Thompson, Angela Abicht, David Beeson, Andrew G. Engel, Bruno Eymard, Emmanuel Maxime, Hanns Lochmüller
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-16 (2018)
Abstract Background Congenital myasthenic syndromes (CMS) are a heterogeneous group of inherited neuromuscular disorders sharing the common feature of fatigable weakness due to defective neuromuscular transmission. Despite rapidly increasing knowledg
Externí odkaz:
https://doaj.org/article/deb2546230134a5a95ce25f9504d37d5
Autor:
Sarah Maguire, Lois J. Surgenor, Daniel Le Grange, Hubert Lacey, Ross D. Crosby, Scott G. Engel, Kirsty M. Fromholtz, Bryony Bamford, Stephen Touyz
Publikováno v:
Journal of Eating Disorders, Vol 5, Iss 1, Pp 1-10 (2017)
Abstract Background An illness staging model for anorexia nervosa (AN) has received increasing attention, but assessing the merits of this concept is dependent on empirically examining a model in clinical samples. Building on preliminary findings reg
Externí odkaz:
https://doaj.org/article/0c6e0c7bc6c64dfbba9b684a08e0f622
Publikováno v:
Medwave, Vol 19, Iss 05, Pp e7645-e7645 (2019)
Introducción Los síndromes miasténicos congénitos son un grupo heterogéneo de desórdenes genéticos, caracterizados por una transmisión sináptica anormal en la placa neuromuscular. Reporte Presentamos el caso de un paciente de dos años,
Externí odkaz:
https://doaj.org/article/fd57b43f39ca4f8ea4b38890b27e6bc7