Telehealth-based exercise in amyotrophic lateral sclerosis by Virginia Kudritzki, Ileana M. Howard, Ileana M. Howard

Subjects: “…amyotrophic lateral sclerosis…”
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Amyotrophic lateral sclerosis: considerations on diagnostic criteria by Marco A. Chieia, Acary S.B. Oliveira, Helga C.A. Silva, Alberto Alain Gabbai

“…Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder, compromising the motor neuron, characterized by progressive muscle weakness, with reserved prognosis. …”
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Urinary symptoms in patients with amyotrophic lateral sclerosis by J.F. Vázquez-Costa, S. Arlandis

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Eosinophils at diagnosis are elevated in amyotrophic lateral sclerosis by Jing Yang, Jing Yang, Jing Yang, Tingting Liu, Tingting Liu, Tingting Liu, Lei Zhang, Xin Li, Xin Li, Xin Li, Feng Ping Du, Feng Ping Du, Feng Ping Du, Qi Liu, Qi Liu, Qi Liu, Hui Dong, Hui Dong, Hui Dong, Yaling Liu, Yaling Liu, Yaling Liu

Subjects: “…amyotrophic lateral sclerosis (ALS)…”
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Laryngeal sensitivity in patients with amyotrophic lateral sclerosis by Giovanni Ruoppolo, Emanuela Onesti, Maria Cristina Gori, Ilenia Schettino, Vittorio Frasca, Antonella Biasiotta, Carla Giordano, Marco Ceccanti, Chiara Cambieri, Antonio Greco, Costantino Buonopane, Giorgio Cruccu, Marco De Vincentiis, Maurizio Inghilleri

Subjects: “…Amyotrophic Lateral Sclerosis…”
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Where and Why Modeling Amyotrophic Lateral Sclerosis by Francesco Liguori, Susanna Amadio, Cinzia Volonté

Subjects: “…amyotrophic lateral sclerosis…”
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Presymptomatic genetic counseling in amyotrophic lateral sclerosis by Yu. A. Shpilyukova, A. A. Rosliakova, M. N. Zakharova, S. N. Illarioshkin

“…Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by progressive loss of central and peripheric motor neurons, with genetic factors playing significant role in its  development. …”
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Structural and functional neuroimaging in amyotrophic lateral sclerosis by Ilya S. Bakulin, Aleksandr V. Chervyakov, Elena I. Kremneva, Rodion N. Konovalov, Maria N. Zakharova

Subjects: “…amyotrophic lateral sclerosis…”
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Dihydrotestosterone in Amyotrophic lateral sclerosis—The missing link? by Nishit Sawal, Jasbinder Kaur, Kamaljeet Kaur, Satinder Gombar

Subjects: “…Amyotrophic Lateral Sclerosis…”
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Synaptic Dysfunction and Plasticity in Amyotrophic Lateral Sclerosis by Rosario Gulino

“…Recent evidence has supported the hypothesis that amyotrophic lateral sclerosis (ALS) is a multi-step disease, as the onset of symptoms occurs after sequential exposure to a defined number of risk factors. …”
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Invertebrate genetic models of amyotrophic lateral sclerosis by LiJun Zhou, LiJun Zhou, RenShi Xu, RenShi Xu

Subjects: “…amyotrophic lateral sclerosis…”
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Diagnostic criteria of amyotrophic lateral sclerosis (ALS) by Reinhard Dengler

Subjects: “…amyotrophic lateral sclerosis…”
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Quantitative FLAIR MRI in amyotrophic lateral sclerosis by Fabes, J, Matthews, L, Filippini, N, Talbot, K, Jenkinson, M, Turner, M

“…<strong>Rationale and Objectives</strong> T2-weighted MRI hyperintensity assessed visually in the corticospinal tract (CST) lacks sensitivity for a diagnosis of amyotrophic lateral sclerosis (ALS). We sought to explore a quantitative approach to FLAIR MRI intensity across a range of ALS phenotypes. …”

Biomarkers in amyotrophic lateral sclerosis: opportunities and limitations. by Bowser, R, Turner, M, Shefner, J

“…Insights into the mechanisms of amyotrophic lateral sclerosis (ALS) have relied predominantly on the study of postmortem tissue. …”

Inflammation and neurovascular changes in amyotrophic lateral sclerosis by Evans, M, Couch, Y, Sibson, N, Turner, MR

“…Neuroinflammation in now established as an important factor in the pathogenesis of many neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS). At various time points, astrocytes and microglia are markedly activated, either producing neuroprotective or pro-inflammatory molecules, which can decrease or increase the rate of primary motor neuron degeneration respectively. …”

The tough body at the epicentre of amyotrophic lateral sclerosis by Turner, M, Menke, R

Sweet food preference in amyotrophic lateral sclerosis by Turner, M, Talbot, K

“…Although tongue electromyography (EMG) was normal, corticobulbar signs were consistent with amyotrophic lateral sclerosis (ALS), a pattern which in the absence of functional impairment outside of speech and swallowing, is appropriately termed progressive bulbar palsy…”

Inflammation and neurovascular changes in amyotrophic lateral sclerosis. by Evans, M, Couch, Y, Sibson, N, Turner, M

“…Neuroinflammation in now established as an important factor in the pathogenesis of many neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS). At various time points, astrocytes and microglia are markedly activated, either producing neuroprotective or pro-inflammatory molecules, which can decrease or increase the rate of primary motor neuron degeneration respectively. …”

Defining pre-symptomatic amyotrophic lateral sclerosis by Benatar, M, Turner, M, Wuu, J

“…This requires an understanding of early/pre-symptomatic disease, a need that is underscored by advances in antisense oligonucleotide, and viral-vector-based gene therapies. In amyotrophic lateral sclerosis (ALS), the study of pre-symptomatic disease requires a cohesive conceptual framework for describing this phase of disease. …”

Quantifying disease progression in amyotrophic lateral sclerosis. by Simon, N, Turner, M, Vucic, S, Al-Chalabi, A, Shefner, J, Lomen-Hoerth, C, Kiernan, M

“…Amyotrophic lateral sclerosis (ALS) exhibits characteristic variability of onset and rate of disease progression, with inherent clinical heterogeneity making disease quantitation difficult. …”