Pages that link to "Q34613895"
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The following pages link to Study of 962 patients indicates progressive muscular atrophy is a form of ALS. (Q34613895):
Displaying 50 items.
- New developments and future opportunities in biomarkers for amyotrophic lateral sclerosis (Q26783410) (← links)
- Differentiating lower motor neuron syndromes (Q28070092) (← links)
- Differential motor neuron involvement in progressive muscular atrophy: a comparative study with amyotrophic lateral sclerosis. (Q30578395) (← links)
- The epidemiology of ALS: a conspiracy of genes, environment and time (Q34377698) (← links)
- Genetic overlap between apparently sporadic motor neuron diseases (Q34479235) (← links)
- Motor neuron disease clinically limited to the lower motor neuron is a diffuse TDP-43 proteinopathy (Q35075257) (← links)
- Lockhart Clarke's contribution to the description of amyotrophic lateral sclerosis (Q35239032) (← links)
- The clinical spectrum of isolated peripheral motor dysfunction (Q35875329) (← links)
- CSF cytokine profile distinguishes multifocal motor neuropathy from progressive muscular atrophy (Q35928735) (← links)
- Acute stimulation of transplanted neurons improves motoneuron survival, axon growth, and muscle reinnervation (Q36947657) (← links)
- Deciphering amyotrophic lateral sclerosis: what phenotype, neuropathology and genetics are telling us about pathogenesis (Q37189268) (← links)
- Transcranial magnetic stimulation and amyotrophic lateral sclerosis: pathophysiological insights (Q37206683) (← links)
- Clinical neurogenetics: amyotrophic lateral sclerosis (Q37274526) (← links)
- Biomarkers in amyotrophic lateral sclerosis: opportunities and limitations (Q37944427) (← links)
- The natural history of motor neuron disease: assessing the impact of specialist care (Q38014082) (← links)
- Clinical and genetic heterogeneity of amyotrophic lateral sclerosis (Q38078984) (← links)
- Diagnostic yield and cost-effectiveness of investigations in patients presenting with isolated lower motor neuron signs (Q38215069) (← links)
- The phenotypic variability of amyotrophic lateral sclerosis (Q38259758) (← links)
- Epigenetic differences between monozygotic twins discordant for amyotrophic lateral sclerosis (ALS) provide clues to disease pathogenesis (Q38644299) (← links)
- The predictive value of respiratory function tests for non-invasive ventilation in amyotrophic lateral sclerosis (Q38661891) (← links)
- Managing pressures ulcers in a resource constrained situation: a holistic approach (Q41004057) (← links)
- Plasma profiling reveals three proteins associated to amyotrophic lateral sclerosis. (Q42173440) (← links)
- MR Spectroscopy Findings in Early Stages of Motor Neuron Disease (Q43858889) (← links)
- SMN1 gene duplications are more frequent in patients with progressive muscular atrophy. (Q44032993) (← links)
- Motoneuron Disease: Clinical (Q45869420) (← links)
- Clinical Spectrum of Amyotrophic Lateral Sclerosis (ALS). (Q46017258) (← links)
- Upper and extra-motoneuron involvement in early motoneuron disease: a diffusion tensor imaging study (Q46092568) (← links)
- Complete hazard ranking to analyze right-censored data: An ALS survival study. (Q47238514) (← links)
- An assessment of treatment guidelines, clinical practices, demographics, and progression of disease among patients with amyotrophic lateral sclerosis in Japan, the United States, and Europe (Q47782678) (← links)
- Quantitative analysis of the features of fasciculation potentials and their relation with muscle strength in amyotrophic lateral sclerosis (Q47956994) (← links)
- White matter pathology in ALS and lower motor neuron ALS variants: a diffusion tensor imaging study using tract-based spatial statistics (Q48651223) (← links)
- Longitudinal course of cortical thickness decline in amyotrophic lateral sclerosis (Q48660838) (← links)
- Accumulation of STIM1 is associated with the degenerative muscle fibre phenotype in ALS and other neurogenic atrophies (Q48701229) (← links)
- Diagnostic contribution of magnetic resonance imaging in an atypical presentation of motor neuron disease. (Q49677520) (← links)
- Non-motor manifestations in ALS patients with tracheostomy and invasive ventilation (Q50145225) (← links)
- Benefit of the Awaji diagnostic algorithm for amyotrophic lateral sclerosis: a prospective study (Q51045774) (← links)
- Amyotrophic lateral sclerosis in Catalonia: a population based study (Q51202335) (← links)
- Fasciculation potentials in amyotrophic lateral sclerosis and the diagnostic yield of the Awaji algorithm (Q51450813) (← links)
- Impairment in Respiratory Function Contributes to Olfactory Impairment in Amyotrophic Lateral Sclerosis. (Q52657184) (← links)
- Progressive muscular atrophy: a patient with confirmatory postmortem findings. (Q53641394) (← links)
- A blended psychosocial support program for partners of patients with amyotrophic lateral sclerosis and progressive muscular atrophy: protocol of a randomized controlled trial. (Q55261083) (← links)
- Association between structural and functional corticospinal involvement in amyotrophic lateral sclerosis assessed by diffusion tensor MRI and triple stimulation technique (Q57274212) (← links)
- ALSUntangled No. 26: Lunasin (Q57464304) (← links)
- Time to generalization and prediction of survival in patients with amyotrophic lateral sclerosis: a retrospective observational study (Q58005566) (← links)
- ALSUntangled No. 28: Acupuncture (Q58125391) (← links)
- Repetitive Nerve Stimulation in Amyotrophic Lateral Sclerosis (Q58714179) (← links)
- Amyotrophic Lateral Sclerosis and its Mimics/Variants: A Comprehensive Review (Q60912737) (← links)
- Motor neuron disease: progressive muscular atrophy in the ALS spectrum (Q84028681) (← links)
- Clinical Reasoning: A case of bilateral foot drop in a 74-year-old man (Q89635921) (← links)
- A robotic neck brace to characterize head-neck motion and muscle electromyography in subjects with amyotrophic lateral sclerosis (Q92492009) (← links)