Amyotrophic lateral sclerosis is a multifactorial disease.
about
Transgenic mice for interleukin 3 develop motor neuron degeneration associated with autoimmune reaction against spinal cord motor neuronsFeasibility of creating a National ALS Registry using administrative data in the United StatesMapping amyotrophic lateral sclerosis lake risk factors across northern New EnglandThe risk of motor neurone disease and multiple sclerosis is different in Estonians and Russians. Data from South Estonia.Dissociated small hand muscle involvement in amyotrophic lateral sclerosis detected by motor unit number estimates.Kinesin mutations cause motor neuron disease phenotypes by disrupting fast axonal transport in DrosophilaExpanding the role of hospice care in amyotrophic lateral sclerosis.Talampanel reduces the level of motoneuronal calcium in transgenic mutant SOD1 mice only if applied presymptomaticallyCurrent pharmacological management of amyotrophic [corrected] lateral sclerosis and a role for rational polypharmacy.State of the field: An informatics-based systematic review of the SOD1-G93A amyotrophic lateral sclerosis transgenic mouse model.Serotonergic mechanisms in amyotrophic lateral sclerosis.Outcomes of physical therapy, speech pathology, and occupational therapy for people with motor neuron disease: a systematic review.Metals in motor neuron diseases.Survey of cannabis use in patients with amyotrophic lateral sclerosis.Administration of 4-(α-L-rhamnosyloxy)-benzyl isothiocyanate delays disease phenotype in SOD1(G93A) rats: a transgenic model of amyotrophic lateral sclerosis.Amyotrophic lateral sclerosis in Mexico: validation of two predictive scales.Expression of a Cu,Zn superoxide dismutase typical of familial amyotrophic lateral sclerosis induces mitochondrial alteration and increase of cytosolic Ca2+ concentration in transfected neuroblastoma SH-SY5Y cells.A differential autophagy-dependent response to DNA double-strand breaks in bone marrow mesenchymal stem cells from sporadic ALS patients.Endogenous female reproductive hormones and the risk of amyotrophic lateral sclerosis.Parental age and the risk of amyotrophic lateral sclerosis.RANTES levels are elevated in serum and cerebrospinal fluid in patients with amyotrophic lateral sclerosisAnalysis of factors that modify susceptibility and rate of progression in amyotrophic lateral sclerosis (ALS)
P2860
Q24313198-4BA2B04E-DD14-4E20-903F-70BDC8EDCD2EQ28389859-8E5F7AB3-95F8-409C-9766-0D1011CBBC93Q28395864-D382B378-50E7-4EC6-B48B-0DF1F9EEA6E1Q31214759-5D9B3CB3-AC3C-420D-80C0-EB9511954F92Q33867364-BE383354-1C9E-4C2E-BE69-862AF8050EA6Q33968701-53ADB34A-557A-45F4-A78D-02B54A0590F6Q34091694-434716B6-4BAA-4CBA-9B48-C8A58ECD27EEQ35595854-A3804FBF-B363-4F63-BB10-97D439CDC7B9Q35753380-3EA39328-5043-43F4-B201-5BF987D02B5AQ36494315-9662C521-5FC4-475C-881D-577A800145CDQ36544155-A4BFF4B6-1BFD-43EF-8C90-8C69714C3366Q36555304-26F23C47-4D28-418A-BEEC-3687D9AEE008Q36612897-4575B9FE-B0F2-4D62-B12C-66F2E8804094Q39382412-F8835FD2-FF73-4F6B-9B57-4D471BDA1353Q40812404-58AF8FFE-4DC7-48EA-8249-A736DA232C7BQ40883419-D3B898C5-B7DA-4645-8096-C398DF2EA2C1Q41088622-9F85FB72-634F-4701-A25B-4F58ED789B83Q42234881-F43FF32B-6060-4813-90D8-2E91A27E2C84Q43937878-CAA39305-598F-4DCE-B3BD-7488771F89CEQ44419383-E5F2F332-192F-4BCE-8D5F-EE786FF932E0Q58125223-ADBD7E20-24D7-4D0E-A9FD-3D6036E32700Q58125280-52F54712-C13A-44A3-A214-CEA58D52A8D4
P2860
Amyotrophic lateral sclerosis is a multifactorial disease.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Amyotrophic lateral sclerosis is a multifactorial disease.
@en
type
label
Amyotrophic lateral sclerosis is a multifactorial disease.
@en
prefLabel
Amyotrophic lateral sclerosis is a multifactorial disease.
@en
P2860
P356
P1433
P1476
Amyotrophic lateral sclerosis is a multifactorial disease.
@en
P2093
P2860
P304
P356
10.1002/MUS.880180711
P577
1995-07-01T00:00:00Z