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Results: 1 to 20 of 1296

Similar articles for PubMed (Select 10430837)

1.

Autosomal dominant juvenile amyotrophic lateral sclerosis.

Rabin BA, Griffin JW, Crain BJ, Scavina M, Chance PF, Cornblath DR.

Brain. 1999 Aug;122 ( Pt 8):1539-50.

2.

Spontaneous activity in electromyography may differentiate certain benign lower motor neuron disease forms from amyotrophic lateral sclerosis.

Jokela ME, Jääskeläinen SK, Sandell S, Palmio J, Penttilä S, Saukkonen A, Soikkeli R, Udd B.

J Neurol Sci. 2015 Jun 3. pii: S0022-510X(15)00341-X. doi: 10.1016/j.jns.2015.06.002. [Epub ahead of print]

PMID:
26059445
3.

Complexities of Genetic Counseling for ALS: A Case of Two Siblings with Discordant Genetic Test Results.

Mandich P, Mantero V, Verdiani S, Gotta F, Caponnetto C, Bellone E, Ferrandes G, Origone P.

J Genet Couns. 2015 Apr 7. [Epub ahead of print]

PMID:
25843563
4.

Laboratory evaluation of suspected motor neuron disease: A survey of physicians.

Sanderson AB, Novak JC, Nash SM, Kolb SJ, Kissel JT.

Muscle Nerve. 2015 Jul;52(1):83-7. doi: 10.1002/mus.24639. Epub 2015 May 14.

PMID:
25736958
5.

Electrophysiological and spinal imaging evidences for sensory dysfunction in amyotrophic lateral sclerosis.

Iglesias C, Sangari S, El Mendili MM, Benali H, Marchand-Pauvert V, Pradat PF.

BMJ Open. 2015 Feb 24;5(2):e007659. doi: 10.1136/bmjopen-2015-007659.

6.

Small-fibre neuropathy related to bulbar and spinal-onset in patients with ALS.

Truini A, Biasiotta A, Onesti E, Di Stefano G, Ceccanti M, La Cesa S, Pepe A, Giordano C, Cruccu G, Inghilleri M.

J Neurol. 2015 Apr;262(4):1014-8. doi: 10.1007/s00415-015-7672-0. Epub 2015 Feb 17.

PMID:
25683764
7.

Importance of sample size for the estimation of repeater F waves in amyotrophic lateral sclerosis.

Fang J, Liu MS, Guan YZ, Cui B, Cui LY.

Chin Med J (Engl). 2015 Feb 20;128(4):515-9. doi: 10.4103/0366-6999.151107.

8.

[Motor nerve hyperexcitability in ALS: its pathophysiology and treatment].

Shibuya K, Misawa S, Kuwabara S.

Rinsho Shinkeigaku. 2014;54(12):1086-8. doi: 10.5692/clinicalneurol.54.1086. Japanese.

PMID:
25672715
9.

[Fasciculation potentials in ALS-significance, and relationship with clinical features].

Bokuda K, Shimizu T.

Rinsho Shinkeigaku. 2014;54(12):1083-5. doi: 10.5692/clinicalneurol.54.1083. Japanese.

PMID:
25672714
10.

Gamma-synuclein pathology in amyotrophic lateral sclerosis.

Peters OM, Shelkovnikova T, Highley JR, Cooper-Knock J, Hortobágyi T, Troakes C, Ninkina N, Buchman VL.

Ann Clin Transl Neurol. 2015 Jan;2(1):29-37. doi: 10.1002/acn3.143. Epub 2014 Dec 12.

11.

[Amyotrophic lateral sclerosis].

Hübers A, Weishaupt JH, Ludolph AC.

Med Monatsschr Pharm. 2014 Oct;37(10):356-64; quiz 365-6. Review. German.

PMID:
25632606
12.

Nerve ultrasound for differentiation between amyotrophic lateral sclerosis and multifocal motor neuropathy.

Grimm A, Décard BF, Athanasopoulou I, Schweikert K, Sinnreich M, Axer H.

J Neurol. 2015 Apr;262(4):870-80. doi: 10.1007/s00415-015-7648-0. Epub 2015 Jan 28.

PMID:
25626722
13.

Mutation analysis of MATR3 in Australian familial amyotrophic lateral sclerosis.

Fifita JA, Williams KL, McCann EP, O'Brien A, Bauer DC, Nicholson GA, Blair IP.

Neurobiol Aging. 2015 Mar;36(3):1602.e1-2. doi: 10.1016/j.neurobiolaging.2014.11.010. Epub 2014 Nov 20.

PMID:
25523636
14.

Mitochondrial abnormalities and low grade inflammation are present in the skeletal muscle of a minority of patients with amyotrophic lateral sclerosis; an observational myopathology study.

Al-Sarraj S, King A, Cleveland M, Pradat PF, Corse A, Rothstein JD, Leigh PN, Abila B, Bates S, Wurthner J, Meininger V.

Acta Neuropathol Commun. 2014 Dec 14;2:165. doi: 10.1186/s40478-014-0165-z.

15.

MicroRNAs as potential circulating biomarkers for amyotrophic lateral sclerosis.

Cloutier F, Marrero A, O'Connell C, Morin P Jr.

J Mol Neurosci. 2015 May;56(1):102-12. doi: 10.1007/s12031-014-0471-8. Epub 2014 Nov 30.

PMID:
25433762
16.

Motor neuron disease with selective degeneration of anterior horn cells associated with non-Hodgkin lymphoma.

Struck AF, Salamat S, Waclawik AJ.

J Clin Neuromuscul Dis. 2014 Dec;16(2):83-9. doi: 10.1097/CND.0000000000000056.

PMID:
25415520
17.

[Comparison of clinical and physiological characteristics between Kennedy disease and amyotrophic lateral sclerosis].

Yang J, Wang Q, Lin L, Wang D, Zheng H, Guan Y.

Nan Fang Yi Ke Da Xue Xue Bao. 2014 Nov;34(11):1688-92. Chinese.

18.

Corneal confocal microscopy reveals trigeminal small sensory fiber neuropathy in amyotrophic lateral sclerosis.

Ferrari G, Grisan E, Scarpa F, Fazio R, Comola M, Quattrini A, Comi G, Rama P, Riva N.

Front Aging Neurosci. 2014 Oct 16;6:278. doi: 10.3389/fnagi.2014.00278. eCollection 2014.

19.

Electrophysiological differences between Hirayama disease, amyotrophic lateral sclerosis and cervical spondylotic amyotrophy.

Jin X, Jiang JY, Lu FZ, Xia XL, Wang LX, Zheng CJ.

BMC Musculoskelet Disord. 2014 Oct 16;15:349. doi: 10.1186/1471-2474-15-349.

20.

Another Perspective on Fasciculations: When is it not Caused by the Classic form of Amyotrophic Lateral Sclerosis or Progressive Spinal Atrophy?

Leite MA, Orsini M, de Freitas MR, Pereira JS, Gobbi FH, Bastos VH, de Castro Machado D, Machado S, Arrias-Carrion O, de Souza JA, Oliveira AB.

Neurol Int. 2014 Aug 8;6(3):5208. doi: 10.4081/ni.2014.5208. eCollection 2014 Aug 5. Review.

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