Results 71 to 80 of about 3,896,599 (361)

Actionable Wearables Data for the Neurology Clinic: A Proof‐of‐Concept Tool

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Wearable devices can monitor key health and fitness domains. In multiple sclerosis (MS), monitoring step count and sleep is feasible, valid, and offers a holistic glimpse of patient functioning and worsening. However, data generated from wearables are typically unavailable at the point of care.
Nicolette Miller   +12 more
wiley   +1 more source

A comparison of the clinical duration and recovery characteristics of cisatracurium after priming using rocuronium or cisatracurium: preliminary study [PDF]

open access: yesKorean Journal of Anesthesiology, 2014
BackgroundThe priming technique can speed up the onset of cisatracurium during intubation. However, there have been no reports on the effect of the priming technique on duration or recovery profile of cisatracurium.
Ki Tae Jung   +3 more
doaj   +1 more source

Home oxygen for children: who, how and when? [PDF]

open access: yes, 2005
A review of the specific requirements of home oxygen therapy in children which attempts to offer guidance to clinicians and service ...
Balfour-Lynn, I.M.   +2 more
core   +2 more sources

Digital Activity Markers in Chronic Inflammatory Demyelinating Polyneuropathy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To evaluate the utility of smartwatch and smartphone‐based activity metrics for assessing disease severity and quality of life in patients with chronic inflammatory demyelinating polyneuropathy (CIDP). Methods In the electronic monitoring of disease activity in patients with CIDP (EMDA‐CIDP) trial, we performed a prospective ...
Lars Masanneck   +15 more
wiley   +1 more source

Proposal for a Revised Classification of the Depth of Neuromuscular Block and Suggestions for Further Development in Neuromuscular Monitoring.

open access: yesAnesthesia and Analgesia, 2019
June 2019 • Volume 128 • Number 6 www.anesthesia-analgesia.org 1361 DOI: 10.1213/ANE.0000000000004065 Anesthesiologists are experiencing new demands for the induction and maintenance of deep neuromuscular block for certain surgical interventions and ...
P. Biro   +3 more
semanticscholar   +1 more source

Multimodal Autonomic Biomarkers Predict Phenoconversion in Pure Autonomic Failure

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Pure autonomic failure (PAF) presents with autonomic failure without other neurological features. A third develop central neurological features, fulfilling criteria for multiple system atrophy (MSA) and Lewy body diseases (LBD), including Parkinson's disease and Dementia with Lewy bodies.
S. Koay   +12 more
wiley   +1 more source

Neuromuscular monitoring in myasthenic syndrome [PDF]

open access: yesAnaesthesia, 2001
We describe the anaesthetic management of a 72‐year‐old man with myasthenic syndrome. Pre‐operatively, he was treated with 3,4‐diaminopyridine and showed a strong hand grip. During general anaesthesia with nitrous oxide and sevoflurane in oxygen, a mechanomyograph and two accelerographs were set up for the hands and left foot to monitor neuromuscular ...
Keizo Shibata, H. Itoh, S. Nitta
openaire   +2 more sources

Feasibility, drug safety, and effectiveness of etiological treatment programs for Chagas disease in Honduras, Guatemala, and Bolivia: 10-year experience of Médecins Sans Frontières [PDF]

open access: yes, 2009
BACKGROUND: Chagas disease (American trypanosomiasis) is a zoonotic or anthropozoonotic disease caused by the parasite Trypanosoma cruzi. Predominantly affecting populations in poor areas of Latin America, medical care for this neglected disease is often
A Valencia   +35 more
core   +4 more sources

Repeat Expansions in PLIN4 Cause Autosomal Dominant Vacuolar Myopathy With Sarcolemmal Features

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective We aim to describe and characterize two unrelated Spanish families suffering from an autosomal dominant autophagic vacuolar myopathy caused by repeat expansions in PLIN4. Methods We evaluated the clinical phenotype and muscle imaging, and performed a genetic workup that included exome sequencing, muscle RNAseq, and long‐read genome ...
Laura Llansó   +17 more
wiley   +1 more source

Neuromuscular Monitoring: Keep It Simple!

open access: yesAnesthesia and Analgesia, 2019
The proposals by Biro et al, 1 which appear in this month’s “Open Mind,” address the future of perioperative neuromuscular monitoring. In essence, their article is an “opinion piece,” which clearly was well received by the peer-review experts of this ...
M. Naguib, A. Kopman
semanticscholar   +1 more source

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