Results 161 to 170 of about 9,262,118 (306)
Miscellaneous sketchbook, 2 [picture] /
Title devised by cataloguer from acquisitions documentation.; Part of the John Power sketchbooks collection.; Condition: Yellowing, soiled, stained, tears.; Also available online at: http://nla.gov.au/nla.pic-vn6293848; Exhibited: Abstraction-Creation: J.
Power, J. J. W. (John Joseph Wardell), 1881-1943.
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Evaluating multi-ancestry genome-wide association methods: Statistical power, population structure, and practical implications. [PDF]
Dias JA +7 more
europepmc +2 more sources
Effect Sizes and Statistical Power in Hearing Aid Research. [PDF]
Pandey P +4 more
europepmc +1 more source
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
Norfolk sketchbook [picture] /
Title devised by cataloguer.; Part of the John Power sketchbooks collection.; Inscriptions: "Norfolk"--In pencil on front cover.; Condition: Yellowing, soiled, stained.; Also available online at: http://nla.gov.au/nla.pic-vn6292751; Exhibited ...
Power, J. J. W. (John Joseph Wardell), 1881-1943.
core
Association Between Motor Pathway Damage and Motor Deficit in Upper and Lower Limb in People With MS
ABSTRACT Objective Corticospinal tract damage is common in people with MS, but the degree of clinical symptoms varies. We hypothesize that corticospinal tract lesions are more extensive and severe in people with MS with motor impairments in both upper and lower limbs.
Mathilde Liffran +13 more
wiley +1 more source
Additional crossovers in cluster randomised crossover trials do not always increase statistical power. [PDF]
Tanvir KM +3 more
europepmc +1 more source
Clinical Impact of NOTCH3 Variant Location After First Stroke in CADASIL
ABSTRACT Objective Despite its monogenic origin, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy exhibits marked variability in clinical expression and severity. Variants in the NOTCH3 gene, within epidermal growth factor‐like repeat domains 1–6 or 7–34, are known to influence disease onset, but their impact ...
Léa Aguilhon +5 more
wiley +1 more source
How to improve statistical power in a trial with SCA2 patients using natural history data. [PDF]
Tran M +7 more
europepmc +1 more source
ABSTRACT Objective Variants in SLC6A1, encoding the GABA transporter 1 (GAT‐1), cause epilepsy, autism spectrum disorder, and developmental delay via loss of GABA uptake, impaired trafficking, and ER retention. We previously found that 4‐Phenylbutyrate (PBA), an FDA‐approved drug, restores GABA uptake and reduces seizures in SLC6A1‐related disorders ...
Melissa B. DeLeeuw +5 more
wiley +1 more source

