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About 21,138 results

ALLMedicine™ Amyotrophic Lateral Sclerosis Center

Research & Reviews  7,363 results

Neurofilament light chain response during therapy with antisense oligonucleotide Tofers...
https://doi.org/10.1002/mus.27818
Muscle & Nerve; Meyer T, Schumann P et. al.

Mar 18th, 2023 - In amyotrophic lateral sclerosis (ALS) caused by superoxide dismutase 1 (SOD1) gene mutations (SOD1-ALS), the antisense oligonucleotide tofersen had been investigated in a phase 3 study (VALOR) and subsequently introduced in an expanded access pro...

Emerging Promise of the Therapeutic Approaches of Mitochondria for Neurodegenerative Di...
https://doi.org/10.2174/1570159X21666230316150559
Current Neuropharmacology; Rahman MM, Tumpa AA et. al.

Mar 18th, 2023 - Mitochondria are critical for homeostasis and metabolism in all cellular eukaryotes. Brain mitochondria are the primary source of fuel that supports many brain functions, including intracellular energy supply, cellular calcium regulation, regulati...

Religiosity in patients with amyotrophic lateral sclerosis, a cross-country comparison.
https://doi.org/10.1007/s11136-023-03383-4
Quality of Life Research : an International Journal of Qu... Ciećwierska K, Lulé D et. al.

Mar 18th, 2023 - Amyotrophic lateral sclerosis (ALS) is a progressive motor impairment leading to early death. Religiousness is one of the factors potentially alleviating the psychological burden of patients. However, its role might vary according to cultural cont...

Expanded access protocol (EAP) program for access to investigational products for amyot...
https://doi.org/10.1002/mus.27819
Muscle & Nerve; Yerton M, Winter A et. al.

Mar 18th, 2023 - Expanded access protocols (EAPs) are a Food and Drug Administration (FDA)-regulated pathway for granting access to investigational products (IPs) to individuals with serious diseases who are ineligible for clinical trials. There is limited informa...

CDNF rescues motor neurons in models of amyotrophic lateral sclerosis by targeting endo...
https://doi.org/10.1093/brain/awad087
Brain : a Journal of Neurology; De Lorenzo F, Lüningschrör P et. al.

Mar 18th, 2023 - Amyotrophic lateral sclerosis is a progressive neurodegenerative disease that affects motor neurons (MNs) in the spinal cord, brainstem, and motor cortex, leading to paralysis and eventually to death within 3 to 5 years of symptom onset. To date, ...

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Guidelines  4 results

Respiratory Management of Patients with Neuromuscular Weakness: An American College of ...
https://doi.org/10.1016/j.chest.2023.03.011
Chest Khan A, Frazer-Green L et. al.

Mar 16th, 2023 - Respiratory failure is a significant concern in neuromuscular diseases (NMD). This CHEST guideline examines the literature on the respiratory management of patients with NMD to provide evidence-based recommendations. An expert panel conducted a sy...

Provisional best practices guidelines for the evaluation of bulbar dysfunction in amyot...
https://doi.org/10.1002/mus.26408
Muscle & Nerve; Pattee GL, Plowman EK et. al.

Jan 9th, 2019 - Universally established comprehensive clinical bulbar scales objectively assessing disease progression in amyotrophic lateral sclerosis (ALS) are currently lacking. The goal of this working group project is to design a best practice set of provisi...

ESPEN guideline clinical nutrition in neurology.
https://doi.org/10.1016/j.clnu.2017.09.003
Clinical Nutrition (Edinburgh, Scotland); Burgos R, Bretón I et. al.

Dec 25th, 2017 - Neurological diseases are frequently associated with swallowing disorders and malnutrition. Moreover, patients with neurological diseases are at increased risk of micronutrient deficiency and dehydration. On the other hand, nutritional factors may...

Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: ...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2764728
Neurology Miller RG, Jackson CE et. al.

Oct 14th, 2009 - To systematically review evidence bearing on the management of patients with amyotrophic lateral sclerosis (ALS). The authors analyzed studies from 1998 to 2007 to update the 1999 practice parameter. Topics covered in this section include breaking...

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Drugs  18 results see all →

Clinicaltrials.gov  554 results

Dazucorilant in Patients With Amyotrophic Lateral Sclerosis
https://clinicaltrials.gov/ct2/show/NCT05407324

Mar 10th, 2023 - Eligible ALS patients will be randomized to one of three treatment arms (1:1:1) across the United States and Europe for a 24-week double-blind treatment period. Patients who complete participation (i.e., complete all visits) in the double-blind tr...

PRE-Symptomatic Studies in Amyotrophic Lateral Sclerosis
https://clinicaltrials.gov/ct2/show/NCT01508962

Mar 10th, 2023 - The goal of PRESS-ALS is to study the earliest manifestations of disease in people with early ALS in whom some areas of the body are not yet affected.

ALS Spinal Cord Gray and White Matter Study
https://clinicaltrials.gov/ct2/show/NCT05764434

Mar 10th, 2023 - This study aims to measure in vivo the spinal cord gray and white matter in patients with Amyotrophic Lateral Sclerosis and healthy persons that match the patients' age and sex using rAMIRA imaging, a novel Magnetic Resonance Imaging (MRI) method....

The Pre-symptomatic Familial Amyotrophic Lateral Sclerosis (Pre-fALS) Study
https://clinicaltrials.gov/ct2/show/NCT00317616

Mar 10th, 2023 - Healthy individuals from fALS families with a known genetic mutation will be included in this study. We encourage people who have previously undergone genetic testing and were found to carry the mutation that affects their family as well as those ...

Speech Analysis in ALS Patients
https://clinicaltrials.gov/ct2/show/NCT03868345

Mar 9th, 2023 - Cognitive dysfunction is increasingly recognized as a core feature of amyotrophic lateral sclerosis (ALS). With appropriate testing, up to 50% of ALS patients will show evidence of frontotemporal dysfunction. Approximately 15% of patients meet for...

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News  488 results

Investigational ALS Drug May Have Clinical Benefit, FDA Staff Says
https://www.medpagetoday.com/neurology/generalneurology/103620

Mar 20th, 2023 - Tofersen, an investigational antisense drug developed to treat amyotrophic lateral sclerosis (ALS) associated with a mutation in the SOD1 gene (SOD1-ALS), may have clinical benefit, FDA reviewers indicated in briefing documents ahead of an advisor...

Dementia Risk Higher for Elite Soccer Players
https://www.medpagetoday.com/neurology/dementia/103563

Mar 16th, 2023 - Men who played elite soccer were more likely to develop neurodegenerative diseases -- notably, dementia -- as they aged, a study in Sweden showed. The risk of neurodegenerative disease was 46% higher among soccer players who played in the Swedish ...

CHEST Unveils Guideline for Respiratory Management of Neuromuscular Diseases
https://www.medpagetoday.com/pulmonology/generalpulmonary/103571

Mar 16th, 2023 - Physicians should incorporate respiratory health care in early treatment plans for patients with neuromuscular diseases (NMD), according to new clinical guidelines from the American College of Chest Physicians (CHEST). Non-invasive ventilation, su...

Epstein-Barr/MS Link; How CBD Curtails Seizures; NIH Finds Rare Neurologic Disease
https://www.medpagetoday.com/neurology/generalneurology/103105

Feb 14th, 2023 - Mounting evidence supports a pivotal role of Epstein-Barr virus in multiple sclerosis (MS), creating opportunities for MS prevention and therapy. (Lancet Neurology) Non-ictal allodynia predicted anti-calcitonin gene-related peptide (CGRP) therapy ...

Viruses Tied to Subsequent Dementia, Other Neurodegenerative Diseases
https://www.medpagetoday.com/neurology/generalneurology/102872

Jan 30th, 2023 - At least 22 viral illnesses were linked with an increased risk of subsequent neurodegenerative disease, NIH researchers found. Using data from the U.K. and Finland, Mike Nalls, PhD, of the NIH Center for Alzheimer's and Related Dementias, and co-a...

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Patient Education  28 results see all →