scholarly article | Q13442814 |
P50 | author | Carolina Barnett | Q59688216 |
P2093 | author name string | Peter Bede | |
Jordan R Green | |||
Yana Yunusova | |||
Emily K Plowman | |||
P2860 | cites work | Primitive reflexes in amyotrophic lateral sclerosis: prevalence and correlates. | Q50853326 |
Amyotrophic lateral sclerosis. Communication status and survival with ventilatory support. | Q51138711 | ||
Needle electromyography of the frontalis muscle in patients with amyotrophic lateral sclerosis. | Q51272870 | ||
Ultrasonographic detection of fasciculations markedly increases diagnostic sensitivity of ALS. | Q51529864 | ||
Multidisciplinary ALS care improves quality of life in patients with ALS. | Q51924828 | ||
Natural history of amyotrophic lateral sclerosis in a database population Validation of a scoring system and a model for survival prediction | Q52340479 | ||
Accuracy, reproducibility and variability of quantitative assessments of bulbar and respiratory function in motor neurone disease. | Q52879999 | ||
The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function. BDNF ALS Study Group (Phase III). | Q53535985 | ||
Subjective experience and coping in ALS | Q54738846 | ||
Assessment of bulbar function in amyotrophic lateral sclerosis: validation of a self-report scale (Center for Neurologic Study Bulbar Function Scale). | Q55664870 | ||
Amyotrophic lateral sclerosis | Q56531747 | ||
Utility of trapezius EMG for diagnosis of amyotrophic lateral sclerosis | Q56772040 | ||
Motor unit number estimation (MUNE): Where are we now? | Q57171769 | ||
Minimally Detectable Change and Minimal Clinically Important Difference of a Decline in Sentence Intelligibility and Speaking Rate for Individuals With Amyotrophic Lateral Sclerosis | Q58096837 | ||
Revisiting the pathoanatomy of pseudobulbar affect: mechanisms beyond corticobulbar dysfunction | Q58125489 | ||
Validation of robust tools to measure sialorrhea in amyotrophic lateral sclerosis: A study in a large French cohort | Q58280431 | ||
Excellent inter‐rater, intra‐rater, and telephone‐administered reliability of the ALSFRS‐R in a multicenter clinical trial | Q58287999 | ||
Amyotrophic Lateral Sclerosis Mimic Syndromes | Q59558037 | ||
Clusters of Deviant Speech Dimensions in the Dysarthrias | Q67213482 | ||
Differential Diagnostic Patterns of Dysarthria | Q67213964 | ||
Electrical impedance myography in the evaluation of the tongue musculature in amyotrophic lateral sclerosis. | Q35842997 | ||
On a Case of Muscular Atrophy, with Disease of the Spinal Cord and Medulla Oblongata | Q36287628 | ||
Predictive value of clinical indices in detecting aspiration in patients with neurological disorders | Q36317197 | ||
Prognostic value of decreased tongue strength on survival time in patients with amyotrophic lateral sclerosis | Q36357161 | ||
Prognostic factors in ALS: A critical review | Q36447824 | ||
Advanced magnetic resonance neuroimaging in bulbar and limb onset early amyotrophic lateral sclerosis | Q36570542 | ||
Defining Swallowing-Related Quality of Life Profiles in Individuals with Amyotrophic Lateral Sclerosis | Q36913504 | ||
Voluntary Cough Airflow Differentiates Safe Versus Unsafe Swallowing in Amyotrophic Lateral Sclerosis | Q36913652 | ||
ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degeneration | Q37593829 | ||
Dysarthria in amyotrophic lateral sclerosis: A review | Q37698625 | ||
Dysphagia in Amyotrophic Lateral Sclerosis: Impact on Patient Behavior, Diet Adaptation, and Riluzole Management | Q37712906 | ||
Trends in Research Literature Describing Dysphagia in Motor Neuron Diseases (MND): A Scoping Review | Q38700978 | ||
Optimizing electrical impedance myography of the tongue in amyotrophic lateral sclerosis | Q39501594 | ||
The COSMIN checklist for assessing the methodological quality of studies on measurement properties of health status measurement instruments: an international Delphi study | Q39973628 | ||
A large-scale multicentre cerebral diffusion tensor imaging study in amyotrophic lateral sclerosis | Q40128196 | ||
Inter- and intrajudge reliability of a clinical examination of swallowing in adults | Q40770365 | ||
Enhanced Bulbar Function in Amyotrophic Lateral Sclerosis: The Nuedexta Treatment Trial. | Q41009555 | ||
Natural history of amyotrophic lateral sclerosis. Observations with the Charing Cross Amyotrophic Lateral Sclerosis Rating Scales. | Q41096180 | ||
A multidisciplinary clinic approach improves survival in ALS: a comparative study of ALS in Ireland and Northern Ireland | Q41637599 | ||
Motor unit number estimation (MUNE) in diseases of the motor neuron: utility and comparative analysis in a multimodal biomarker study. | Q42935383 | ||
Grey matter correlates of clinical variables in amyotrophic lateral sclerosis (ALS): a neuroimaging study of ALS motor phenotype heterogeneity and cortical focality | Q43739867 | ||
Focal thinning of the motor cortex mirrors clinical features of amyotrophic lateral sclerosis and their phenotypes: a neuroimaging study | Q44215931 | ||
Clinical features that distinguish PLS, upper motor neuron-dominant ALS, and typical ALS. | Q45261558 | ||
Spontaneous electromyographic activity of the tongue in amyotrophic lateral sclerosis | Q45734377 | ||
Decreased brain activation to tongue movements in amyotrophic lateral sclerosis with bulbar involvement but not Kennedy syndrome | Q46057525 | ||
Recombinant growth hormone treatment of amyotrophic lateral sclerosis | Q46170423 | ||
Speech deterioration in amyotrophic lateral sclerosis (ALS) after manifestation of bulbar symptoms. | Q47605893 | ||
A retrospective investigation of the relationship between baseline covariates and rate of ALSFRS-R decline in ALS clinical trials | Q47772089 | ||
What does the ALSFRS-R really measure? A longitudinal and survival analysis of functional dimension subscores in amyotrophic lateral sclerosis | Q48033371 | ||
Maximum Tongue Pressure is Associated with Swallowing Dysfunction in ALS Patients. | Q48256179 | ||
Cortical thickness in ALS: towards a marker for upper motor neuron involvement | Q48605539 | ||
Electromyography of sternocleidomastoid muscle in ALS: a prospective study | Q48613779 | ||
Tracking motor neuron loss in a set of six muscles in amyotrophic lateral sclerosis using the Motor Unit Number Index (MUNIX): a 15-month longitudinal multicentre trial. | Q48671390 | ||
The segmental diffusivity profile of amyotrophic lateral sclerosis associated white matter degeneration | Q48721254 | ||
A protocol for identification of early bulbar signs in amyotrophic lateral sclerosis | Q48733582 | ||
Multimodal spinal cord MRI offers accurate diagnostic classification in ALS. | Q49899544 | ||
Investigating the neuroanatomical substrate of pathological laughing and crying in amyotrophic lateral sclerosis with multimodal neuroimaging techniques | Q50072712 | ||
The diagnostic utility of patient-report and speech-language pathologists' ratings for detecting the early onset of bulbar symptoms due to ALS. | Q50204979 | ||
The evaluation of bulbar dysfunction in amyotrophic lateral sclerosis: survey of clinical practice patterns in the United States | Q50347043 | ||
Interobserver reliability and perceptual ratings: more than meets the ear | Q68295880 | ||
The effect of rate control on the intelligibility and naturalness of dysarthric speech | Q68876881 | ||
A double-blind, placebo-controlled trial of high doses of gangliosides in amyotrophic lateral sclerosis | Q69556043 | ||
Amyotrophic lateral sclerosis severity scale | Q69617955 | ||
The administration of guanidine in amyotrophic lateral sclerosis | Q69822558 | ||
A rating scale for amyotrophic lateral sclerosis: description and preliminary experience | Q70365353 | ||
Multiple orofacial indices in amyotrophic lateral sclerosis | Q72257979 | ||
Physiologic deficits in the orofacial system underlying dysarthria in amyotrophic lateral sclerosis | Q72390734 | ||
The relative value of facial, glossal, and masticatory muscles in the electrodiagnosis of amyotrophic lateral sclerosis | Q73115227 | ||
Videofluoroscopic evaluation of dysphagia in motor neurone disease with modified barium swallow | Q73151887 | ||
Radiological evidence of subclinical dysphagia in motor neuron disease | Q74560386 | ||
Needle electromyography of bulbar muscles in patients with amyotrophic lateral sclerosis: evidence of subclinical involvement | Q77568382 | ||
Listener agreement for auditory-perceptual ratings of dysarthria | Q80138042 | ||
Carcinoma of the tongue and bulbar-onset amyotrophic lateral sclerosis: unusual differential diagnosis | Q80551928 | ||
Longitudinal analysis of progression of dysphagia in amyotrophic lateral sclerosis | Q80556866 | ||
ALSFRS and appel ALS scores: discordance with disease progression | Q80742099 | ||
Utility of clinical swallowing examination measures for detecting aspiration post-stroke | Q82552034 | ||
Patterns of cortical activity differ in ALS patients with limb and/or bulbar involvement depending on motor tasks | Q82719806 | ||
Evaluation of swallowing pressure in a patient with amyotrophic lateral sclerosis before and after cricopharyngeal myotomy using high-resolution manometry system | Q82980830 | ||
Clinical identification of dysarthria types among neurologists, residents in neurology and speech therapists | Q83494604 | ||
Development of a new scale for dysphagia in patients with progressive neuromuscular diseases: the Neuromuscular Disease Swallowing Status Scale (NdSSS) | Q85527047 | ||
Changes in tongue pressure, pulmonary function, and salivary flow in patients with amyotrophic lateral sclerosis | Q85655722 | ||
Evidence of multidimensionality in the ALSFRS-R Scale: a critical appraisal on its measurement properties using Rasch analysis | Q86443331 | ||
Reliability of measurements of tongue and hand strength and endurance using the Iowa Oral Performance Instrument with elderly adults | Q87934077 | ||
Gray Matter Volume Changes over the Whole Brain in the Bulbar- and Spinal-onset Amyotrophic Lateral Sclerosis: a Voxel-based Morphometry Study | Q88276553 | ||
The changing landscape of motor neuron disease imaging: the transition from descriptive studies to precision clinical tools | Q88640722 | ||
Cortical Thinning Pattern of Bulbar- and Spinal-onset Amyotrophic Lateral Sclerosis: a Surface-based Morphometry Study | Q89432497 | ||
Deconstructing progression of amyotrophic lateral sclerosis in stages: a Markov modeling approach | Q89994562 | ||
Additional evidence for a therapeutic effect of dextromethorphan/quinidine on bulbar motor function in patients with amyotrophic lateral sclerosis: A quantitative speech analysis | Q91176815 | ||
Automatic extraction of abnormal lip movement features from the alternating motion rate task in amyotrophic lateral sclerosis | Q91731412 | ||
Mimics and chameleons in motor neurone disease | Q24619538 | ||
Laryngeal dysfunction in Amyotrophic Lateral Sclerosis: a review and case report | Q24795457 | ||
Lessons of ALS imaging: Pitfalls and future directions - A critical review | Q26860864 | ||
El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis | Q29619074 | ||
Profiling Speech and Pausing in Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD) | Q30392615 | ||
Predicting Early Bulbar Decline in Amyotrophic Lateral Sclerosis: A Speech Subsystem Approach | Q30407658 | ||
A novel fixed-target task to determine articulatory speed constraints in persons with amyotrophic lateral sclerosis | Q30459549 | ||
Algorithmic Estimation of Pauses in Extended Speech Samples of Dysarthric and Typical Speech | Q30480544 | ||
Discriminant ability of the Eating Assessment Tool-10 to detect aspiration in individuals with amyotrophic lateral sclerosis. | Q30691863 | ||
Guidelines for using quantitative measures of brain magnetic resonance imaging abnormalities in monitoring the treatment of multiple sclerosis | Q32067610 | ||
Comparison of the King's and MiToS staging systems for ALS. | Q33659132 | ||
Ultra high-field (7tesla) magnetic resonance spectroscopy in Amyotrophic Lateral Sclerosis | Q33675140 | ||
Multimodal assessment of white matter tracts in amyotrophic lateral sclerosis | Q33757517 | ||
Consensus guidelines for the design and implementation of clinical trials in ALS. World Federation of Neurology committee on Research | Q33762409 | ||
Voxel-based MRI intensitometry reveals extent of cerebral white matter pathology in amyotrophic lateral sclerosis | Q34061536 | ||
A Case of Amyotrophic Lateral Sclerosis Presented as Oropharyngeal Dysphagia | Q34129367 | ||
Improving the quality of life for people with ALS: the challenge ahead | Q34314315 | ||
ALSFRS-R. | Q34362989 | ||
Communication Support for People with ALS. | Q34986955 | ||
Predicting prognosis in amyotrophic lateral sclerosis: a simple algorithm | Q35747193 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Cosmin | Q1136134 |
amyotrophic lateral sclerosis | Q206901 | ||
dysarthria | Q225957 | ||
P304 | page(s) | 106 | |
P577 | publication date | 2019-01-01 | |
P1433 | published in | Frontiers in Neurology | Q15817039 |
P1476 | title | Clinical Measures of Bulbar Dysfunction in ALS | |
P478 | volume | 10 |
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