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amyotrophic lateral sclerosis
rare neurodegenerative disease with amyotrophy and progressive paralysis
Details
- Subclass of
- motor neuron disease, TDP-43 Proteinopathies, monogenic disease
- afflicts
- motor neuron
- genetic association
- ITGA9, CTNND2, TSPAN9, TFAP2A, ATP2B2, EPB41, LRRC8C, NFASC, SLC25A12, ERBB4, TRPM8, KCNMB2
- health specialty
- neurology
- ICD-9-CM
- 335.20
- ICPC 2 ID
- N99
- medical examination
- Awaji Criteria
- named after
- Lou Gehrig, Jean-Martin Charcot
- nickname
- Lou Gehrig's disease
- short name
- ELA, ALS
- topic has template
- Template:Amyotrophic lateral sclerosis
- topic's main category
- Category:Amyotrophic lateral sclerosis
Connected on Wikidata
Subject of
- ALS Awareness Month
- Min kamp mot tiden
- genetics of amyotrophic lateral sclerosis
- amyotrophic lateral sclerosis research
- Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders
- Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Phase 1 Dose Escalation and PK Study of Cu(II)ATSM in ALS/MND
- Neuromuscular Magnetic Stimulation in ALS Patients
- A Study to Evaluate the Safety, Tolerability and Efficacy of ILB in Patients With Amyotrophic Lateral Sclerosis
- A Systematic Investigation of Phonetic Complexity Effects on Articulatory Motor Performance in Progressive Dysarthria
- Music Therapy Protocol to Support Bulbar and Respiratory Functions in ALS
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