Results 141 to 150 of about 236,334 (314)

METHOD OF CHARACTERISTICS FOR DESIGN OF CENTRIFUGAL PUMP GEOMETRY

open access: yesTASK Quarterly, 2010
The method of characteristics leads to the blade geometry of a centrifugal pump. The method is built taking the advantage of the governing equations of fluid mechanics written in a non-orthogonal coordinates system.
ROMUALD PUZYREWSKI   +2 more
doaj  

To pump or not to pump; paediatric insulin pump efficacy [PDF]

open access: yesEndocrine Abstracts, 2015
Mariam Rahm, Sermed Mezher
openaire   +1 more source

White Matter Hyperintensity Burden and Short‐Interval Change Associated With Sleep Apnoea in the UK Biobank

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Purpose White matter hyperintensities (WMH) are a core neuroimaging marker of cerebral small vessel disease (CSVD). Sleep apnoea (SA) is a recognized vascular risk factor, but its associations with regional WMH burden, short‐interval WMH change and cognitive performance in population‐based cohorts remain incompletely defined. We
Peng Cheng   +4 more
wiley   +1 more source

The Investigation of Pump Performance and Evaluation over the Internet

open access: yes, 2010
Selection and configuration are widely met tasks in design; this is an example of a web-based selection/configuration tool with embedded optimisation.
Webb, DC, Darbyshire, K, Waterworth, G
core  

Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach   +23 more
wiley   +1 more source

Pipeline Extension from Wellhead to Hand Pumps in Villages [PDF]

open access: yes, 2012
This technical briefing note looks at the criteria for selecting ‘Pipeline Extension from Wellhead to Hand Pumps in Villages’ in all settings (e.g.

core  

Risk of Non‐Arteritic Anterior Ischemic Optic Neuropathy in Idiopathic Intracranial Hypertension Patients Treated with GLP‐1 Receptor Agonists

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Introduction Glucagon‐like peptide‐1 receptor agonists (GLP‐1 RAs) have demonstrated significant weight‐reducing effects and may offer benefits in idiopathic intracranial hypertension (IIH); however, recent concerns about the risk of non‐arteritic anterior ischemic optic neuropathy (NAION) have emerged.
Faisal A. Al‐Harbi   +9 more
wiley   +1 more source

Compound Heterozygote Friedreich Ataxia Patients With Covert Proximal FXN Gene Deletions

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT We present Friedreich ataxia patients with frataxin gene deletions. Data and records were collected at the Children's Hospital of Philadelphia from patients enrolled in the FACOMS natural history study. Patients with proximal deletions initially diagnosed with only one GAA expanded allele had more severe disease than their homozygous expansion
Michael P. Lazaropoulos   +5 more
wiley   +1 more source

Pressure–Flow Rate Characteristics of the Pumps with Permanent Magnets

open access: yes
Theoretical and experimental modelling investigations have demonstrated that electromagnetic induction pumps based on the principle of rotating permanent magnets (PMP) have many advantages in comparison with traditional linear inductor pumps [1].
Krišbergs, Rihards   +2 more
core  

Recurrent Hypothermia and Autonomic Dysfunction Secondary to Shapiro Syndrome

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT A 44‐year‐old man presented with recurrent hypothermia, diaphoresis and hypertension. Extensive investigation for infectious, inflammatory, metabolic and endocrine aetiologies was negative. MR scan of the brain demonstrated no lesions but revealed callosal dysgenesis, consistent with Shapiro syndrome.
Naveen Kumar   +3 more
wiley   +1 more source

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