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hereditary motor neuron disease相关文献:
Motor Neuron Disease: Pathophysiology, Diagnosis, and Management.
Foster LA, Salajegheh MK.
Am J Med. 2019 Jan;132(1):32-37. doi: 10.1016/j.amjmed.2018.07.012. Epub 2018 Aug 1.
PMID:30075105
Motor neuron diversity in development and disease.
Kanning KC, Kaplan A, Henderson CE.
Annu Rev Neurosci. 2010;33:409-40. doi: 10.1146/annurev.neuro.051508.135722.
PMID:20367447
Atypical Motor Neuron Disease variants: Still a diagnostic challenge in Neurology.
Pinto WBVR, Debona R, Nunes PP, Assis ACD, Lopes CG, Bortholin T, Dias RB, Naylor FGM, Chieia MAT, Souza PVS, Oliveira ASB.
Rev Neurol (Paris). 2019 Apr;175(4):221-232. doi: 10.1016/j.neurol.2018.04.016. Epub 2019 Mar 4.
PMID:30846210
Differentiating lower motor neuron syndromes.
Garg N, Park SB, Vucic S, Yiannikas C, Spies J, Howells J, Huynh W, Matamala JM, Krishnan AV, Pollard JD, Cornblath DR, Reilly MM, Kiernan MC.
J Neurol Neurosurg Psychiatry. 2017 Jun;88(6):474-483. doi: 10.1136/jnnp-2016-313526. Epub 2016 Dec 21.
PMID:28003344
The epidemiology of amyotrophic lateral sclerosis.
Talbott EO, Malek AM, Lacomis D.
Handb Clin Neurol. 2016;138:225-38. doi: 10.1016/B978-0-12-802973-2.00013-6.
PMID:27637961
Hereditary spastic paraplegia: More than an upper motor neuron disease.
Parodi L, Fenu S, Stevanin G, Durr A.
Rev Neurol (Paris). 2017 May;173(5):352-360. doi: 10.1016/j.neurol.2017.03.034. Epub 2017 Apr 24.
PMID:28449883
Amyotrophic Lateral Sclerosis and Other Motor Neuron Diseases.
Izenberg A.
Continuum (Minneap Minn). 2023 Oct 1;29(5):1538-1563. doi: 10.1212/CON.0000000000001345.
PMID:37851042
Progressive Muscular Atrophy.
Liewluck T, Saperstein DS.
Neurol Clin. 2015 Nov;33(4):761-73. doi: 10.1016/j.ncl.2015.07.005.
PMID:26515620
Amyotrophic Lateral Sclerosis and Other Motor Neuron Diseases.
Quinn C, Elman L.
Continuum (Minneap Minn). 2020 Oct;26(5):1323-1347. doi: 10.1212/CON.0000000000000911.
PMID:33003004
Hereditary canine spinal muscular atrophy: an animal model of motor neuron disease.
Cork LC.
Can J Neurol Sci. 1991 Aug;18(3 Suppl):432-4. doi: 10.1017/s0317167100032613.
PMID:1933694
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