Results 131 to 140 of about 167,787,432 (216)
Annals 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
Ireland sketchbook [picture] /
, 1930 Title devised by cataloguer.; Part of the John Power sketchbooks collection.; Inscriptions: "Ireland"--In pencil on front cover.; Condition: Yellowing, soiled, stained, tears, loss.; Also available online at: http://nla.gov.au/nla.pic-vn6293748 ...
Power, J. J. W. (John Joseph Wardell), 1881-1943.
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Clinical Impact of NOTCH3 Variant Location After First Stroke in CADASIL
Annals of Clinical and Translational Neurology, EarlyView.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
Asia, Europe and Canada sketchbook [picture] /
, 1930 Title devised by cataloguer.; Part of the John Power sketchbooks collection.; Condition: Yellowing, soiled, stained, tears.; Also available online at: http://nla.gov.au/nla.pic-vn6294112; Exhibited: Abstraction-Creation: J.W.
Power, J. J. W. (John Joseph Wardell), 1881-1943.
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Annals of Clinical and Translational Neurology, EarlyView.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
, 1930 Title devised by cataloguer.; Part of the John Power sketchbooks collection.; Inscriptions: "India"--In pencil on front cover.; Condition: Yellowing, soiled, stained.; Also available online at: http://nla.gov.au/nla.pic-vn6293781; Exhibited: Abstraction ...
Power, J. J. W. (John Joseph Wardell), 1881-1943.
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Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective To clarify the clinical relevance of dopamine transporter single‐photon emission computed tomography (DAT‐SPECT) abnormalities in amyotrophic lateral sclerosis (ALS), with a prespecified focus on sex‐stratified associations with disease progression and short‐term prognosis.
Tomoya Kawazoe +7 more
wiley +1 more source
, 1935 Title devised by cataloguer from inscriptions.; Part of the John Power sketchbooks collection.; Inscriptions: "Bournemouth + spares"--In pencil on front cover.; Condition: Yellowing, soiled, stained.; Also available online at: http://nla.gov.au/nla.pic ...
Power, J. J. W. (John Joseph Wardell), 1881-1943, artist.
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Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Facioscapulohumeral muscular dystrophy (FSHD) is one of the most debilitating and common muscular dystrophies. Despite its severity, no approved therapy exists for FSHD patients. However, several therapeutic candidates are currently under development, and some have recently entered clinical trials, marking the need for reliable ...
Mustafa Bilal Bayazit +11 more
wiley +1 more source
Australian views and figures studies sketchbook [picture] /
, 1930 Title devised by cataloguer.; Part of the John Power sketchbooks collection.; Condition: Yellowing, soiled, stained.; Also available online at: http://nla.gov.au/nla.pic-vn6294140; Exhibited: Abstraction-Creation: J.W.
Power, J. J. W. (John Joseph Wardell), 1881-1943.
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