#Als emg findings manual#
#Als emg findings trial#

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis/Riluzole Study Group II. Dose-ranging study of riluzole in amyotrophic lateral sclerosis. Lacomblez L, Bensimon G, Leigh PN, Guillet P, Meininger V.

#Als emg findings trial#

A controlled trial of riluzole in amyotrophic lateral sclerosis. Oxidative stress biomarkers in sporadic ALS. Mitsumoto H, Santella RM, Liu X, Bogdanov M, Zipprich J, Wu HC, et al. Increased lipid peroxidation in sera of ALS patients: a potential biomarker of disease burden. Simpson EP, Henry YK, Henkel JS, Smith RG, Appel SH. Oxidative damage to protein in sporadic motor neuron disease spinal cord. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Rosen DR, Siddique T, Patterson D, Figlewicz DA, Sapp P, Hentati A, et al. Current hypotheses for the underlying biology of amyotrophic lateral sclerosis. Molecular and cellular pathways of neurodegeneration in motor neurone disease. Progress in clinical neurosciences: the evidence for ALS as a multisystems disorder of limited phenotypic expression. Oxidative stress in ALS: key role in motor neuron injury and therapeutic target. Amyotroph Lateral Scler Frontotemporal Degener. Primary lateral sclerosis: predicting functional outcome. 72(12):1087-94.Īlmeida V, de Carvalho M, Scotto M, Pinto S, Pinto A, Ohana B, et al. Natural history and clinical features of the flail arm and flail leg ALS variants. Wijesekera LC, Mathers S, Talman P, Galtrey C, Parkinson MH, Ganesalingam J, et al. 51(6):1546-54.Ĭlinical and neuropathological criteria for frontotemporal dementia. Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. California: Published by the LLU Department of Neurology, Loma Linda 2007.

#Als emg findings manual#

A manual for patients, families and friends. ALS 1996 and Beyond: New Hopes and Challenges. ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degeneration. Amyotrophic Lateral Sclerosis: A Patient Care Guide for Clinicians. Neurodegenerative diseases target large-scale human brain networks. Seeley WW, Crawford RK, Zhou J, Miller BL, Greicius MD. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. 72(2):257-68.ĭeJesus-Hernandez M, Mackenzie IR, Boeve BF, Boxer AL, Baker M, Rutherford NJ, et al. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Renton AE, Majounie E, Waite A, Simón-Sánchez J, Rollinson S, Gibbs JR, et al. Can regional spreading of amyotrophic lateral sclerosis motor symptoms be explained by prion-like propagation?. The motor neuron diseases and related disorders. An estimate of amyotrophic lateral sclerosis heritability using twin data. 65 Suppl 1:S17-23.Īl-Chalabi A, Fang F, Hanby MF, Leigh PN, Shaw CE, Ye W, et al. Managing amyotrophic lateral sclerosis: slowing disease progression and improving patient quality of life. The management of amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis: A 40-year personal perspective. Living with amyotrophic lateral sclerosis/motor neurone disease (ALS/MND): decision-making about 'ongoing change and adaptation'. Clinical diagnosis and management of amyotrophic lateral sclerosis. Practice parameter update: The care of the patient with amyotrophic lateral sclerosis: multidisciplinary care, symptom management, and cognitive/behavioral impairment (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology. Miller RG, Jackson CE, Kasarskis EJ, et al. Report of the Quality Standards Subcommittee of the American Academy of Neurology. Practice Parameter update: The care of the patient with amyotrophic lateral sclerosis: Drug, nutritional, and respiratory therapies (an evidence-based review). Miller RG, Jackson CE, Kasarskis EJ et al.

Amyotroph Lateral Scler Other Motor Neuron Disord. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. American Academy of Neurology Guidelineīrooks BR, Miller RG, Swash M, Munsat TL.Needle Electromyography and Nerve Conduction Studies.