(2000). El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders: Vol. 1, No. 5, pp. 293-299.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders Template
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About the Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders format
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders is a peer-reviewed journal published by Taylor & Francis, covering Amyotrophic Lateral Sclerosis Research, Neurogenetic and Muscular Disorders Research, Genetic Neurodegenerative Diseases.
| Publisher | Taylor & Francis |
|---|---|
| Reference style | Author–year (Chicago, T&F) Author–year — (Smith, 2023) in the text Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders 12 (3): 45–58.
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| Publishes research in | Amyotrophic Lateral Sclerosis Research Neurogenetic and Muscular Disorders Research Genetic Neurodegenerative Diseases Parkinson's Disease Mechanisms and Treatments Neurological diseases and metabolism |
| ISSN | 1466-0822 |
| h-index | 48 |
| i10-index | 197 |
| Total citations | 14,992 |
| Top institutions publishing here | California Pacific Medical Center |
| Journal website | www.tandfonline.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
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Most-cited papers in Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders
BACKGROUND: Brain derived neurotrophic factor (BDNF) is a potent survival factor for motoneurons. This study investigated the safety and tolerability of recombinant methionyl human BDNF (r-metHuBDNF) infused intrathecally by means of an implanted pump in patients with ALS. METHODS: Twenty-five patients with probable or definite ALS were treated with either r-metHuBDNF (25, 60, 150, 400…
OBJECTIVE: Since the discovery of mutations in the gene encoding Cu/Zn superoxide dismutase (SOD1) ten years ago, testing for SOD1 gene mutations has become a part of the investigation of patients with suspected motor neuron disease. We searched for novel SOD1 mutations and for clinical characteristics of patients with these mutations. METHODS: Analysis was made…
INTRODUCTION: Increasing evidence suggests that oxidative stress may be involved in the pathogenesis of amyotrophic lateral sclerosis (ALS). The antioxidant vitamin E (alpha-tocopherol) has been shown to slow down the onset and progression of paralysis in transgenic mice expressing a mutation in superoxide dismutase found in certain forms of familial ALS. The current study was…
INTRODUCTION: Recently it has been shown in animal models of amyotrophic lateral sclerosis (ALS) that stem cells significantly slow the progression of the disease and prolong survival. We have evaluated the feasibility and safety of a method of intraspinal cord implantation of autologous mesenchymal stem cells (MSCs) in a few well-monitored patients with ALS. METHOD:…