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Items: 1 to 20 of 147

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.

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
3.

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
4.

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
5.

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
6.

Onset and spreading patterns of upper and lower motor neuron symptoms in amyotrophic lateral sclerosis.

Körner S, Kollewe K, Fahlbusch M, Zapf A, Dengler R, Krampfl K, Petri S.

Muscle Nerve. 2011 May;43(5):636-42. doi: 10.1002/mus.21936.

PMID:
21484822
7.

Onset and spreading patterns of lower motor neuron involvements predict survival in sporadic amyotrophic lateral sclerosis.

Fujimura-Kiyono C, Kimura F, Ishida S, Nakajima H, Hosokawa T, Sugino M, Hanafusa T.

J Neurol Neurosurg Psychiatry. 2011 Nov;82(11):1244-9. doi: 10.1136/jnnp-2011-300141. Epub 2011 Sep 15.

PMID:
21921087
8.

[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
10.

Survival rate of patients with amyotrophic lateral sclerosis in Wakayama Prefecture, Japan, 1966 to 2005.

Kihira T, Yoshida S, Okamoto K, Kazimoto Y, Ookawa M, Hama K, Miwa H, Kondo T.

J Neurol Sci. 2008 May 15;268(1-2):95-101. doi: 10.1016/j.jns.2007.11.011. Epub 2007 Dec 31.

PMID:
18164728
11.

Evaluation and rehabilitation of patients with adult motor neuron disease.

Francis K, Bach JR, DeLisa JA.

Arch Phys Med Rehabil. 1999 Aug;80(8):951-63. Review.

PMID:
10453774
12.

[Epidemiology of amyotrophic lateral sclerosis].

Soriani MH, Desnuelle C.

Rev Neurol (Paris). 2009 Aug-Sep;165(8-9):627-40. doi: 10.1016/j.neurol.2009.04.004. Epub 2009 Jun 13. Review. French.

PMID:
19524991
13.

Hereditary pure lower motor neuron disease with adult onset and rapid progression.

Van den Berg-Vos RM, Van den Berg LH, Jansen GH, Parton M, Shaw CE, Hesseling-Janssen AL, Wokke JH.

J Neurol. 2001 Apr;248(4):290-6.

PMID:
11374093
14.

Study of motor asymmetry in ALS indicates an effect of limb dominance on onset and spread of weakness, and an important role for upper motor neurons.

Devine MS, Kiernan MC, Heggie S, McCombe PA, Henderson RD.

Amyotroph Lateral Scler Frontotemporal Degener. 2014 Dec;15(7-8):481-7. doi: 10.3109/21678421.2014.906617. Epub 2014 May 9.

PMID:
24809721
15.

Amyotrophic lateral sclerosis. Insights from genetics.

Brown RH Jr.

Arch Neurol. 1997 Oct;54(10):1246-50. Review.

PMID:
9341570
16.

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
17.

Isolated bulbar phenotype of amyotrophic lateral sclerosis.

Burrell JR, Vucic S, Kiernan MC.

Amyotroph Lateral Scler. 2011 Jul;12(4):283-9. doi: 10.3109/17482968.2011.551940.

PMID:
21702735
18.

The pseudopolyneuritic form of amyotrophic lateral sclerosis (Patrikios' disease).

Cappellari A, Ciammola A, Silani V.

Electromyogr Clin Neurophysiol. 2008 Mar;48(2):75-81.

PMID:
18435211
19.

Demographic characteristics and prognosis in a Flemish amyotrophic lateral sclerosis population.

Thijs V, Peeters E, Theys P, Matthijs G, Robberecht W.

Acta Neurol Belg. 2000 Jun;100(2):84-90.

PMID:
10934559
20.

Multiple orofacial indices in amyotrophic lateral sclerosis.

DePaul R, Brooks BR.

J Speech Hear Res. 1993 Dec;36(6):1158-67.

PMID:
8114482
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