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Amyotrophic Lateral Sclerosis 4, Juvenile

Known as: ALS4, NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES 
National Institutes of Health

Papers overview

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2019
2019
Four new chalcohalides Ba3AlQ4X (Q = S, Se; X = Cl, Br) have been discovered by a conventional high-temperature method. All of… 
2017
2017
We report a 44 years old man with slowly progressive muscular atrophy of the extremities for over 30 years. He experienced… 
2016
2016
Objective: To determine whether GGGGCC (G4C2) repeat expansions at loci other than C9orf72 serve as common causes of amyotrophic… 
2014
2014
Development of Alzheimer's disease (AD) is characterized by progressive neuronal death and a decline in learning and memory… 
2012
2012
Amyotrophic lateral sclerosis 4 (ALS4), a rare form of autosomal dominant juvenile-onset ALS characterised by slow progression… 
Review
2011
Review
2011
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive muscle weakness that reflects… 
2005
2005
OBJECTIVE To observe the different mRNA levels of Candida albicans ALS gene family between planktonic and biofilm-grown cells… 
2003
2003
To determine whether Charcot-Marie-Tooth (CMT) with pyramidal features is genetically distinct from other dominantly inherited… 
2002
2002
AI-sensitive (als) mutants of Arabidopsis were isolated and characterized with the aim of defining mechanisms of AI toxicity and… 
2000
2000
  • Xi ChenJ. Chen
  • 2000
  • Corpus ID: 37329241
With a 0.5 kb probe of CX2, distribution of CX2 tandem repeats was studied in different C.albicans strains. Results suggest that…