Results 61 to 70 of about 411,754 (345)
The Case of a 28‐Year‐Old Woman With Medically Refractory Focal Epilepsy
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT We present the case of a 28‐year‐old right‐handed woman with medically refractory focal epilepsy. Her seizure semiology and electroencephalography (EEG) indicated a seizure onset zone in the right central‐parietal area. However, both MRI and PET scans were unremarkable, showing no focal lesions or areas of altered metabolism.
Rishi Sharma +5 more
wiley +1 more source
The Impact of Smart Phone Applications on Improving Marketing Performance of Banking Services in Jordanian Commercial Banks [PDF]
, 2022 Researcher- Amman Arab University
openalex +1 more source
Acoustic Measures Capture Speech Dysfunction in Spinocerebellar Ataxia
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Spinocerebellar ataxias (SCA) are hereditary cerebellar degenerative disorders with a common feature of dysarthria, involving impaired phonatory and articulatory control of speech, thereby affecting social communication. In this study, we investigated whether acoustic measures could objectively measure speech dysfunction and identify
Zena Fadel +5 more
wiley +1 more source
BASSA: New software tool reveals hidden details in visualisation of low‐frequency animal sounds
Ecology and EvolutionThe study of animal sounds in biology and ecology relies heavily upon time–frequency (TF) visualisation, most commonly using the short‐time Fourier transform (STFT) spectrogram.
Benjamin A. Jancovich, Tracey L. Rogers
doaj +1 more source
The Case of a 37‐Year‐Old Woman Presenting With Subacute Weakness and Paresthesias
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Acute intermittent porphyria (AIP) is a rare metabolic disorder that may present with subacute neuropathy and systemic symptoms, often leading to diagnostic delay. We report a 37‐year‐old woman with eight weeks of progressive bilateral upper extremity weakness and paresthesias, followed by lower extremity involvement and falls, in the setting ...
Peter Pacut +3 more
wiley +1 more source
Anatomical and spectrographic analysis of the voice in disease: A report of five cases
South African Journal of Communication Disorders, 1973 Five cases are presented. One is a case of ventricular phonation of iatrogenic origin and the remaining four had undergone laryngectomy for carcinoma of the larynx. Points of interest are discussed, particularly the constant ventricular fold phonation of
W. A. Kerr, L. W. Lanham
doaj +1 more source
Neuropsychiatric Symptoms Mimicking Dementia in a Patient Treated With Imatinib
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Tyrosine kinase inhibitors are the cornerstone of chronic myeloid leukemia treatment. Newer agents have more potency and a broader spectrum of action, but also a higher potential for neuropsychiatric side effects. We present a case of a patient on imatinib who developed progressive cognitive, mood, and behavioral alterations.
Ashley Jones +3 more
wiley +1 more source
Applying an Ethical Lens to the Treatment of People With Multiple Sclerosis
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT The practice of neurology requires an understanding of clinical ethics for decision‐making. In multiple sclerosis (MS) care, there are a wide range of ethical considerations that may arise. These involve shared decision‐making around selection of a disease‐modifying therapy (DMT), risks and benefits of well‐studied medications in comparison to
Methma Udawatta, Farrah J. Mateen
wiley +1 more source
Effects of vocalization training on drooling severity in Parkinson's disease
Chinese Journal of Contemporary Neurology and Neurosurgery, 2019 Objective To investigate the effect of vocalization training in improving drooling in patients with Parkinson's disease (PD). Methods A total of 60 PD patients from August 2018 to July 2019 were randomly divided into control group (N = 30) and ...
Qing⁃ling FENG +7 more
doaj
Clinically Relevant Outcome Measures in Women With Adrenoleukodystrophy
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Adrenoleukodystrophy is a rare inherited peroxisomal disease caused by pathogenic variants in the ABCD1 gene located on the X chromosome. Although the most severe central nervous system and adrenal complications typically affect only men with adrenoleukodystrophy, the majority of women develop myeloneuropathy symptoms in adulthood.
Chenwei Yan +3 more
wiley +1 more source