Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Kay W P Ng"'
Autor:
Ryan W Johnson, Kay W P Ng, Alexander R Dietz, Mary E Hartman, Jack D Baty, Nausheen Hasan, Craig M Zaidman, Michael Shoykhet
Publikováno v:
PLoS ONE, Vol 13, Iss 12, p e0207720 (2018)
IMPORTANCE:ICU-acquired muscle atrophy occurs commonly and worsens outcomes in adults. The incidence and severity of muscle atrophy in critically ill children are poorly characterized. OBJECTIVE:To determine incidence, severity and risk factors for m
Externí odkaz:
https://doaj.org/article/a1c12ae16db14c6382b328f15e4d50dc
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
Polymyxin-induced neuromuscular blockade is a rare but potentially fatal condition, with majority of cases that were reported between 1962 and 1973. We describe a patient who developed hypercapnic respiratory failure after initiation of polymyxin for
Externí odkaz:
https://doaj.org/article/1188e3fd80e749a2ad2def2c5cd57e67
Publikováno v:
Frontiers in neurology. 13
The diagnosis of inherited neuromuscular disorders is challenging due to their genetic and phenotypic variability. Traditionally, neurophysiology and histopathology were primarily used in the initial diagnostic approach to these conditions. Sanger se
Publikováno v:
Muscle & Nerve. 59:88-94
Introduction We evaluated the reliability of measuring muscle thickness with ultrasound in limbs and diaphragms of critically ill children and determined the sensitivity of these measures to quantitate muscle atrophy over time. Methods An expert and
Autor:
Nausheen Hasan, Ryan Johnson, Kay W. P. Ng, Alexander R. Dietz, Michael Shoykhet, Craig M. Zaidman, Mary E. Hartman, Jack Baty
Publikováno v:
PLoS ONE, Vol 13, Iss 12, p e0207720 (2018)
PLoS ONE
PLoS ONE
Importance ICU-acquired muscle atrophy occurs commonly and worsens outcomes in adults. The incidence and severity of muscle atrophy in critically ill children are poorly characterized. Objective To determine incidence, severity and risk factors for m
Publikováno v:
Stroke Research and Treatment, Vol 2011 (2011)
Our knowledge about various inherited and acquired causes of thrombophilic disorders has increased significantly during the past decade. Technology for various diagnostic tests for these rare disorders has matched the rapid advances in our understand
Externí odkaz:
https://doaj.org/article/9e76e803542f42d28848418e2f997519