Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 185

1.

Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study.

Chiò A, Calvo A, Moglia C, Mazzini L, Mora G; PARALS study group.

J Neurol Neurosurg Psychiatry. 2011 Jul;82(7):740-6. doi: 10.1136/jnnp.2010.235952. Epub 2011 Mar 14.

PMID:
21402743
2.

Variability and prognostic relevance of different phenotypes in amyotrophic lateral sclerosis - data from a population-based registry.

Wolf J, Safer A, Wöhrle JC, Palm F, Nix WA, Maschke M, Grau AJ.

J Neurol Sci. 2014 Oct 15;345(1-2):164-7. doi: 10.1016/j.jns.2014.07.033. Epub 2014 Jul 19.

PMID:
25086855
3.

Identification and outcomes of clinical phenotypes in amyotrophic lateral sclerosis/motor neuron disease: Australian National Motor Neuron Disease observational cohort.

Talman P, Duong T, Vucic S, Mathers S, Venkatesh S, Henderson R, Rowe D, Schultz D, Edis R, Needham M, Macdonnell R, McCombe P, Birks C, Kiernan M.

BMJ Open. 2016 Sep 30;6(9):e012054. doi: 10.1136/bmjopen-2016-012054.

4.

Natural history and clinical features of the flail arm and flail leg ALS variants.

Wijesekera LC, Mathers S, Talman P, Galtrey C, Parkinson MH, Ganesalingam J, Willey E, Ampong MA, Ellis CM, Shaw CE, Al-Chalabi A, Leigh PN.

Neurology. 2009 Mar 24;72(12):1087-94. doi: 10.1212/01.wnl.0000345041.83406.a2.

5.

Natural history of young-adult amyotrophic lateral sclerosis.

Sabatelli M, Madia F, Conte A, Luigetti M, Zollino M, Mancuso I, Lo Monaco M, Lippi G, Tonali P.

Neurology. 2008 Sep 16;71(12):876-81. doi: 10.1212/01.wnl.0000312378.94737.45. Epub 2008 Jul 2.

PMID:
18596241
6.

Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS.

Sabatelli M, Zollino M, Luigetti M, Grande AD, Lattante S, Marangi G, Monaco ML, Madia F, Meleo E, Bisogni G, Conte A.

Amyotroph Lateral Scler. 2011 Jul;12(4):278-82. doi: 10.3109/17482968.2011.580849.

PMID:
21702734
7.

Amyotrophic Lateral Sclerosis Regional Variants (Brachial Amyotrophic Diplegia, Leg Amyotrophic Diplegia, and Isolated Bulbar Amyotrophic Lateral Sclerosis).

Jawdat O, Statland JM, Barohn RJ, Katz JS, Dimachkie MM.

Neurol Clin. 2015 Nov;33(4):775-85. doi: 10.1016/j.ncl.2015.07.003. Epub 2015 Sep 8. Review.

8.

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
9.

Abnormalities in cortical and peripheral excitability in flail arm variant amyotrophic lateral sclerosis.

Vucic S, Kiernan MC.

J Neurol Neurosurg Psychiatry. 2007 Aug;78(8):849-52. Epub 2007 Jan 8.

10.

[A study of bulbar, upper extremity, and lower extremity motor function preservation at the time that respiratory symptoms appear in ALS].

Kimura F, Fujimura C, Ishida S, Hosokawa T, Sato T, Nakajima H, Furutama D, Sugino M.

Rinsho Shinkeigaku. 2007 Apr;47(4):140-6. Japanese.

PMID:
17511283
11.

Diagnostic and Prognostic Biomarkers in Amyotrophic Lateral Sclerosis: Neurofilament Light Chain Levels in Definite Subtypes of Disease.

Gaiani A, Martinelli I, Bello L, Querin G, Puthenparampil M, Ruggero S, Toffanin E, Cagnin A, Briani C, Pegoraro E, Sorarù G.

JAMA Neurol. 2017 May 1;74(5):525-532. doi: 10.1001/jamaneurol.2016.5398.

12.

Clinical phenotypes and natural progression for motor neuron disease: analysis from an Australian database.

Talman P, Forbes A, Mathers S.

Amyotroph Lateral Scler. 2009 Apr;10(2):79-84. doi: 10.1080/17482960802195871.

PMID:
18608095
13.

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
14.

Clinical Spectrum of Amyotrophic Lateral Sclerosis (ALS).

Grad LI, Rouleau GA, Ravits J, Cashman NR.

Cold Spring Harb Perspect Med. 2017 Aug 1;7(8). pii: a024117. doi: 10.1101/cshperspect.a024117. Review.

PMID:
28003278
15.

Focal thinning of the motor cortex mirrors clinical features of amyotrophic lateral sclerosis and their phenotypes: a neuroimaging study.

Schuster C, Kasper E, Machts J, Bittner D, Kaufmann J, Benecke R, Teipel S, Vielhaber S, Prudlo J.

J Neurol. 2013 Nov;260(11):2856-64. doi: 10.1007/s00415-013-7083-z. Epub 2013 Aug 31.

PMID:
23996101
16.

Clinical epidemiology of amyotrophic lateral sclerosis in Liguria, Italy: An update of LIGALS register.

Scialò C, Novi G, Bandettini di Poggio M, Canosa A, Sormani MP, Mandich P, Origone P, Truffelli R, Mancardi GL, Caponnetto C.

Amyotroph Lateral Scler Frontotemporal Degener. 2016 Oct - Nov;17(7-8):535-542. Epub 2016 Jul 11.

PMID:
27399231
17.

Identifying who will benefit from non-invasive ventilation in amyotrophic lateral sclerosis/motor neurone disease in a clinical cohort.

Berlowitz DJ, Howard ME, Fiore JF Jr, Vander Hoorn S, O'Donoghue FJ, Westlake J, Smith A, Beer F, Mathers S, Talman P.

J Neurol Neurosurg Psychiatry. 2016 Mar;87(3):280-6. doi: 10.1136/jnnp-2014-310055. Epub 2015 Apr 9.

PMID:
25857659
18.

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
19.

Rapidly progressive amyotrophic lateral sclerosis initially masquerading as a demyelinating neuropathy.

Ahdab R, Créange A, Saint-Val C, Farhat WH, Lefaucheur JP.

Neurophysiol Clin. 2013 Jun;43(3):181-7. doi: 10.1016/j.neucli.2013.05.001. Epub 2013 May 18.

PMID:
23856174
20.

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

Supplemental Content

Support Center