Results 71 to 80 of about 25,555 (216)
Movement Disorders Clinical Practice, EarlyView.Abstract Background Lower urinary tract symptoms (LUTS) are among the most prevalent nonmotor complaints across the parkinsonian spectrum, yet they remain underutilized as diagnostic and management signals in neurology practice. Although prior reviews have characterized disease‐specific patterns of urinary dysfunction, and recent guidelines address ...
Saar Anis +3 more
wiley +1 more source
Behavioral Disorders in Association with Posterior Callosal and Frontal Cerebral Infarction
Behavioural Neurology, 1993 Behavioral disorders were a prominent clinical feature after the surgical treatment of an anterior communicating artery aneurysm rupture in a 44-year-old man. Callosal apraxia was associated with an alien hand.
J. P. Lejeune, D. Caparros-Lefebvre
doaj +1 more source
Frontiers in Human Neuroscience, 2014 The feeling of acting voluntarily is a fundamental component of human behavior and social life and is usually accompanied by a sense of agency. However, this ability can be impaired in a number of diseases and disorders.
Mariella ePazzaglia +2 more
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Movement Disorders, EarlyView.Abstract Background CSF1R‐related disorder (CSF1R‐RD) is a severe autosomal dominant leukoencephalopathy characterized by progressive cognitive, neuropsychiatric, and motor decline. Although genetic testing is widely available, numerous likely pathogenic variants in CSF1R frequently remain classified as variants of uncertain significance (VUS ...
Charles Wade +8 more
wiley +1 more source
The academic responses to the apraxia objection
Praxis Filosófica, 2018 In this paper, I reconstruct and analyze the Academic skeptics’ responses to the apraxia objection. This objection claims that the scepticism is a doctrine impossible to be put into practice because its theses lead to apraxia, that is, a state of lack or
Christian F. Pineda-Pérez
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Developmental Medicine &Child Neurology, EarlyView.This systematic overview highlights communication impairment as a defining feature of Rett syndrome, with expressive language consistently affected more severely than receptive language and social ability. Across the literature, most studies rely on caregiver‐reported measures, with relatively few employing direct or objective measurements of speech ...
Lucas N. Raniolo +6 more
wiley +1 more source
Phonological analysis of substitution errors of patients with apraxia of speech
Dementia & NeuropsychologiaThe literature on apraxia of speech describes the types and characteristics of phonological errors in this disorder. In general, phonemes affected by errors are described, but the distinctive features involved have not yet been investigated.
Maysa Luchesi Cera, Karin Zazo Ortiz
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Genetic testing in paediatric neurological disorders
Developmental Medicine &Child Neurology, EarlyView.In this study 390 paediatric patients with neurological disorders underwent genetic testing via exome sequencing, commercial panel, in‐house epilepsy, and movement disorder gene panels. Exome sequencing provides the highest diagnostic yield, and severe developmental delay and hypotonia predicted pathogenic variants in the exome sequencing cohort ...
Wafa Bani Uraba +15 more
wiley +1 more source
Developmental Medicine &Child Neurology, EarlyView.Abstract Aim To map diagnostic procedures and standardized instruments reportedly used to identify autism spectrum disorder (ASD) in people with cerebral palsy or other early‐onset motor conditions (EOMC) including Rett syndrome and muscular dystrophy.
Olga Laporta‐Hoyos +11 more
wiley +1 more source