Amyotrophic Lateral Sclerosis
What's New
Last Posted: Apr 02, 2024
- Fluctuating salience in those living with genetic risk of motor neuron disease: A qualitative interview study.
Jade Howard et al. Health Expect 2024 27(2) e14024 - Harnessing Big Data in Amyotrophic Lateral Sclerosis: Machine Learning Applications for Clinical Practice and Pharmaceutical Trials.
Ee Ling Tan et al. J Integr Neurosci 2024 23(3) 58 - Amyotrophic lateral sclerosis: translating genetic discoveries into therapies.
Fulya Akçimen et al. Nat Rev Genet 2023 4 (9) 642-658 - Ensemble-imbalance-based classification for amyotrophic lateral sclerosis prognostic prediction: identifying short-survival patients at diagnosis.
Fabiano Papaiz et al. BMC Med Inform Decis Mak 2024 24(1) 80 - Individuals' experiences in genetic counseling and predictive testing for familial amyotrophic lateral sclerosis.
Connolly G Steigerwald et al. J Genet Couns 2024 - Predicting amyotrophic lateral sclerosis (ALS) progression with machine learning.
Muzammil Arif Din Abdul Jabbar et al. Amyotroph Lateral Scler Frontotemporal Degener 2023 1-14 - The implications of DNA methylation for amyotrophic lateral sclerosis.
Adriana Helena DE Oliveira Reis et al. An Acad Bras Cienc 2023 95(suppl 2) e20230277 - Incorporating Genetic Testing Into the Care of Patients With Amyotrophic Lateral Sclerosis/Frontotemporal Degeneration Spectrum Disorders.
Chelsea Chambers et al. Neurol Clin Pract 2023 13(5) e200201 - Evidence-based consensus guidelines for ALS genetic testing and counseling.
Jennifer Roggenbuck et al. Ann Clin Transl Neurol 2023 - Rare variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genome
JP Ross et al, Genetics in Medicine, August 25, 2023 - At-home wearables and machine learning sensitively capture disease progression in amyotrophic lateral sclerosis
AS Gupta et al, Nature Comm. August 21, 2023 - SOD1-ALS-Browser: a web-utility for investigating the clinical phenotype in SOD1 amyotrophic lateral sclerosis.
Thomas P Spargo et al. Amyotroph Lateral Scler Frontotemporal Degener 2023 1-10 - PROSA-a multicenter prospective observational study to develop low-burden digital speech biomarkers in ALS and FTD.
Johannes Tröger et al. Amyotroph Lateral Scler Frontotemporal Degener 2023 1-10 - Genetic screening for Huntington disease phenocopies in Sweden: A tertiary center case series focused on short tandem repeat (STR) disorders.
Martin Paucar et al. J Neurol Sci 2023 451120707 - Shared genetic risk loci between Alzheimer's disease and related dementias, Parkinson's disease, and amyotrophic lateral sclerosis.
Michael Wainberg et al. Alzheimers Res Ther 2023 15(1) 113 - Clinical and molecular features of patients with amyotrophic lateral sclerosis and SOD1 mutations: a monocentric study.
Delia Gagliardi et al. Front Neurol 2023 141169689 - Advantages of routine next generation sequencing over standard genetic testing in the ALS clinic.
Jakub Scaber et al. Eur J Neurol 2023 - Clinical and genetic features of amyotrophic lateral sclerosis patients with C9orf72 mutations.
Maximilian Wiesenfarth et al. Brain communications 2023 5(2) fcad087 - Clinical testing panels for ALS: global distribution, consistency, and challenges.
Allison A Dilliott et al. Amyotrophic lateral sclerosis & frontotemporal degeneration 2023 1-16 - Wearable device and smartphone data quantify ALS progression and may provide novel outcome measures
SA Johnson et al, NPJ Digital Medicine, March 6, 2023
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About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Page last updated:May 01, 2024
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