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Items: 1 to 20 of 110

1.

Neck weakness is a potent prognostic factor in sporadic amyotrophic lateral sclerosis patients.

Nakamura R, Atsuta N, Watanabe H, Hirakawa A, Watanabe H, Ito M, Senda J, Katsuno M, Tanaka F, Izumi Y, Morita M, Ogaki K, Taniguchi A, Aiba I, Mizoguchi K, Okamoto K, Hasegawa K, Aoki M, Kawata A, Abe K, Oda M, Konagaya M, Imai T, Nakagawa M, Tsuji S, Kaji R, Nakano I, Sobue G.

J Neurol Neurosurg Psychiatry. 2013 Dec;84(12):1365-71. doi: 10.1136/jnnp-2013-306020. Epub 2013 Aug 9.

PMID:
23933739
2.

Factors affecting longitudinal functional decline and survival in amyotrophic lateral sclerosis patients.

Watanabe H, Atsuta N, Nakamura R, Hirakawa A, Watanabe H, Ito M, Senda J, Katsuno M, Izumi Y, Morita M, Tomiyama H, Taniguchi A, Aiba I, Abe K, Mizoguchi K, Oda M, Kano O, Okamoto K, Kuwabara S, Hasegawa K, Imai T, Aoki M, Tsuji S, Nakano I, Kaji R, Sobue G.

Amyotroph Lateral Scler Frontotemporal Degener. 2015 Jun;16(3-4):230-6. doi: 10.3109/21678421.2014.990036. Epub 2014 Dec 30.

PMID:
25548957
3.

Age of onset differentially influences the progression of regional dysfunction in sporadic amyotrophic lateral sclerosis.

Yokoi D, Atsuta N, Watanabe H, Nakamura R, Hirakawa A, Ito M, Watanabe H, Katsuno M, Izumi Y, Morita M, Taniguchi A, Oda M, Abe K, Mizoguchi K, Kano O, Kuwabara S, Kaji R, Sobue G; JaCALS.

J Neurol. 2016 Jun;263(6):1129-36. doi: 10.1007/s00415-016-8109-0. Epub 2016 Apr 15.

PMID:
27083563
4.

Early or late appearance of "dropped head syndrome" in amyotrophic lateral sclerosis.

Gourie-Devi M, Nalini A, Sandhya S.

J Neurol Neurosurg Psychiatry. 2003 May;74(5):683-6. Review.

5.

Motor responses of the sternocleidomastoid muscle in patients with amyotrophic lateral sclerosis.

Pinto S, de Carvalho M.

Muscle Nerve. 2008 Oct;38(4):1312-7. doi: 10.1002/mus.21109.

PMID:
18785186
6.

Clinical features that distinguish PLS, upper motor neuron-dominant ALS, and typical ALS.

Gordon PH, Cheng B, Katz IB, Mitsumoto H, Rowland LP.

Neurology. 2009 Jun 2;72(22):1948-52. doi: 10.1212/WNL.0b013e3181a8269b.

PMID:
19487653
7.

Regionality of disease progression predicts prognosis in amyotrophic lateral sclerosis.

van der Kleij LA, Jones AR, Steen IN, Young CA, Shaw PJ, Shaw CE, Leigh PN, Turner MR, Al-Chalabi A.

Amyotroph Lateral Scler Frontotemporal Degener. 2015;16(7-8):442-7. doi: 10.3109/21678421.2015.1051987. Epub 2015 Jun 17.

PMID:
26083873
8.

[The changes of clinical characteristics in 100 Japanese amyotrophic lateral sclerosis patients between 1980 and 2000].

Kimura F, Shinoda K, Fujiwara S, Fujimura C, Nakajima H, Furutama D, Sugino M, Hanafusa T.

Rinsho Shinkeigaku. 2003 Jul;43(7):385-91. Japanese.

PMID:
14582363
9.

The amyotrophic lateral sclerosis functional rating scale predicts survival time in amyotrophic lateral sclerosis patients on invasive mechanical ventilation.

Lo Coco D, Marchese S, La Bella V, Piccoli T, Lo Coco A.

Chest. 2007 Jul;132(1):64-9. Epub 2007 May 2.

PMID:
17475635
10.

Patterns of clinical and electrodiagnostic abnormalities in early amyotrophic lateral sclerosis.

Simon NG, Lomen-Hoerth C, Kiernan MC.

Muscle Nerve. 2014 Dec;50(6):894-9. doi: 10.1002/mus.24244. Epub 2014 Oct 31.

PMID:
24647900
11.

Rate of disease progression: a prognostic biomarker in ALS.

Labra J, Menon P, Byth K, Morrison S, Vucic S.

J Neurol Neurosurg Psychiatry. 2016 Jun;87(6):628-32. doi: 10.1136/jnnp-2015-310998. Epub 2015 Jul 7.

PMID:
26152368
12.

Motor axonal excitability properties are strong predictors for survival in amyotrophic lateral sclerosis.

Kanai K, Shibuya K, Sato Y, Misawa S, Nasu S, Sekiguchi Y, Mitsuma S, Isose S, Fujimaki Y, Ohmori S, Koga S, Kuwabara S.

J Neurol Neurosurg Psychiatry. 2012 Jul;83(7):734-8. doi: 10.1136/jnnp-2011-301782. Epub 2012 May 7.

PMID:
22566594
13.

Phase angle is a prognostic factor for survival in amyotrophic lateral sclerosis.

Desport JC, Marin B, Funalot B, Preux PM, Couratier P.

Amyotroph Lateral Scler. 2008 Oct;9(5):273-8. doi: 10.1080/17482960801925039.

PMID:
18720089
14.

An Objective Functional Characterisation of Head Movement Impairment in Individuals with Neck Muscle Weakness Due to Amyotrophic Lateral Sclerosis.

Pancani S, Tindale W, Shaw PJ, McDermott CJ, MazzĂ  C.

PLoS One. 2017 Jan 9;12(1):e0169019. doi: 10.1371/journal.pone.0169019. eCollection 2017.

15.

Natural history and clinical features of sporadic amyotrophic lateral sclerosis in China.

Chen L, Zhang B, Chen R, Tang L, Liu R, Yang Y, Yang Y, Liu X, Ye S, Zhan S, Fan D.

J Neurol Neurosurg Psychiatry. 2015 Oct;86(10):1075-81. doi: 10.1136/jnnp-2015-310471. Epub 2015 Jun 29.

PMID:
26124198
16.

The predictors of survival in Chinese amyotrophic lateral sclerosis patients.

Wei Q, Chen X, Zheng Z, Guo X, Huang R, Cao B, Zeng Y, Shang H.

Amyotroph Lateral Scler Frontotemporal Degener. 2015 Jun;16(3-4):237-44. doi: 10.3109/21678421.2014.993650. Epub 2015 Jan 12.

PMID:
25581512
17.

The diagnostic pathway and prognosis in bulbar-onset amyotrophic lateral sclerosis.

Turner MR, Scaber J, Goodfellow JA, Lord ME, Marsden R, Talbot K.

J Neurol Sci. 2010 Jul 15;294(1-2):81-5. doi: 10.1016/j.jns.2010.03.028. Epub 2010 May 10.

PMID:
20452624
18.

Prediction of prognosis of ALS: Importance of active denervation findings of the cervical-upper limb area and trunk area.

Sato Y, Nakatani E, Watanabe Y, Fukushima M, Nakashima K, Kannagi M, Kanatani Y, Mizushima H.

Intractable Rare Dis Res. 2015 Nov;4(4):181-9. doi: 10.5582/irdr.2015.01043.

20.

Targeted assessment of lower motor neuron burden is associated with survival in amyotrophic lateral sclerosis.

Devine MS, Ballard E, O'Rourke P, Kiernan MC, Mccombe PA, Henderson RD.

Amyotroph Lateral Scler Frontotemporal Degener. 2016;17(3-4):184-90. doi: 10.3109/21678421.2015.1125502. Epub 2015 Dec 24.

PMID:
26700804

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