مكتبة

Source: npj Genomic Medicine, Vol 7, Iss 1, Pp 1-8 (2022)npj Genomic MedicineAl Khleifat, A, Iacoangeli, A, van Vugt, J J F A, Bowles, H, Moisse, M, Zwamborn, R A J, van der Spek, R A A, Shatunov,

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Gene therapy for ALS: A review

Authors : Defne A. Amado; Beverly L. Davidson

Subjects: Genetic enhancement; Gene delivery; Bioinformatics

Source: Molecular Therapy. 29:3345-3358

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Healthcare Utilisation and Satisfaction with Care in Patients with Amyotrophic Lateral Sclerosis - An Observational Study

Authors : Charlotte Ytterberg; Kristina Gottberg; Petter Sandstedt

Subjects: Male; Research Report; medicine.medical_specialty

Source: Journal of Neuromuscular Diseases

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MATR3 F115C knock-in mice do not exhibit motor defects or neuropathological features of ALS

Authors : Xiao Xiao Lily Chen; Justin You; Jihye Rachel Kim

Subjects: 0301 basic medicine; Motor Disorders; Mutant

Source: Biochemical and Biophysical Research Communications. 568:48-54

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Native Separation and Metallation Analysis of SOD1 Protein from the Human Central Nervous System: a Methodological Workflow

Authors : Glenda M. Halliday; Benjamin G. Trist; Asuncion Carmona ...

Subjects: SOD1; Central nervous system; Context (language use)

Source: Analytical ChemistryAnalytical Chemistry, American Chemical Society, 2021, 93 (32), pp.11108-11115. ⟨10.1021/acs.analchem.1c01128⟩Analytical chemistry 93(32), 11108-11115 (2021).

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Demystifying the spontaneous phenomena of motor hyperexcitability

Authors : Christopher Shaw; W.K. Chan; F. Norwood

Subjects: Neuromyotonia; Context (language use); Electromyography

Source: Clinical Neurophysiology. 132:1830-1844

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A survey on patients' disease perception and the impact of the COVID-19 pandemic on persons living with amyotrophic lateral sclerosis in Malaysia

Authors : Khean Jin Goh; Suzanna Edgar; Ee Chin Loh

Subjects: Adult; Male; Health Knowledge, Attitudes, Practice

Source: Neurodegenerative Disease Management

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Association between Body Composition and Dysphagia in Patients with Amyotrophic Lateral Sclerosis

Authors : Gabriela Menegatti; Rosana M Borges; Helena N M Sierra

Subjects: amyotrophic lateral sclerosis; medicine.medical_specialty; Neurosciences. Biological psychiatry. Neuropsychiatry

Source: Neurology International, Vol 13, Iss 32, Pp 315-327 (2021)Neurology InternationalVolume 13Issue 3Pages 32-327

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نتائج البحث

فلترة النتائج

A bioinformatic inquiry of the EAAT2 interactome in postmortem and neuropsychiatric datasets

Engaging Specialist Palliative Care in the Management of Amyotrophic Lateral Sclerosis: A Patient-, Family-, and Provider-Based Approach

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis

Gene therapy for ALS: A review

Healthcare Utilisation and Satisfaction with Care in Patients with Amyotrophic Lateral Sclerosis - An Observational Study

MATR3 F115C knock-in mice do not exhibit motor defects or neuropathological features of ALS

Native Separation and Metallation Analysis of SOD1 Protein from the Human Central Nervous System: a Methodological Workflow

Demystifying the spontaneous phenomena of motor hyperexcitability

A survey on patients' disease perception and the impact of the COVID-19 pandemic on persons living with amyotrophic lateral sclerosis in Malaysia

Association between Body Composition and Dysphagia in Patients with Amyotrophic Lateral Sclerosis

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