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The latter approach has much higher computational complexity limiting its use in motor diagnostics applications.
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The impact of elevated body fat on motor coordination diagnostic assessments in children with DCD has not been established.
Although α-synuclein fibrillisation and Lewy body formation in human brain are the key and essential pathogenic process in PD, substantial loss of dopaminergic neurons is more likely responsible for the onset of the clinical motor symptoms diagnostic of PD.
All patients fulfilled the clinical diagnostic criteria according to the UK Parkinson's Disease Society Brain Bank and subsequently developed dementia more than a year from onset of motor symptoms (Diagnostic and Statistical Manual of Mental Disorders Fourth Edition (DSM IV); APA, 1994), or met the revised consensus criteria for DLB.
The other one is to understand how we can build new applications that carmakers have not thought about yet, on top of these new smart and connected platforms". "We can also connect physically to the car's control network (CAN) that gives you access to all the vehicle's data (diagnostic, motor power, drivetrain, battery power, pedal position...), but that'll be less fun," joked Musquet.
Although these symptoms can also develop after the clinical diagnosis of PD, for this review, we focus on the period prior to the emergence of diagnostic motor abnormalities.
Concurrent and discriminant validity have been assessed by comparing the Pediatric Outcomes Data Collection Instrument with other measures of health and well-being, gross motor function and diagnostic subgroups in children with CP [ 43].
In 2004, she founded Nanobiosym Labs as a research organization to develop her theories on how molecular motors work and Nanobiosym Diagnostics to create technologies to take advantage of her findings.
Incorporation of needle electromyographic evidence of lower motor neuron degeneration into diagnostic criteria has undoubtedly advanced diagnosis, but even earlier diagnosis might be possible by including tests of subclinical upper motor neuron disease.
Manifest HD was defined as carrying the HTT CAG repeat expansion mutation (≥36) and having a motor score with a diagnostic confidence of four on the UHDRS motor scale (37).
We investigated the association between subject's Hoehn & Yahr (H&Y) stage, Mini-Mental State Examination (MMSE), age, and motor symptom subgroups and diagnostic performance of ioflupane [I] imaging.
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