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Similar articles for PubMed (Select 9341570)

1.

Amyotrophic lateral sclerosis. Insights from genetics.

Brown RH Jr.

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

PMID:
9341570
2.

Primary lateral sclerosis as a phenotypic manifestation of familial ALS.

Brugman F, Wokke JH, Vianney de Jong JM, Franssen H, Faber CG, Van den Berg LH.

Neurology. 2005 May 24;64(10):1778-9.

PMID:
15911810
3.

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.

4.

Mechanisms for neuronal degeneration in amyotrophic lateral sclerosis and in models of motor neuron death (Review).

Martin LJ, Price AC, Kaiser A, Shaikh AY, Liu Z.

Int J Mol Med. 2000 Jan;5(1):3-13. Review.

PMID:
10601567
5.

Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patients.

Andersen PM, Forsgren L, Binzer M, Nilsson P, Ala-Hurula V, Keränen ML, Bergmark L, Saarinen A, Haltia T, Tarvainen I, Kinnunen E, Udd B, Marklund SL.

Brain. 1996 Aug;119 ( Pt 4):1153-72. Erratum in: Brain 1998 Jan;121(Pt 1):187.

7.

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
8.

A molecular genetic approach to amyotrophic lateral sclerosis.

Siddique T, Hu P, Hentati A, Deng G, Hung WY, McInnis MG, Warren AC, Rimmler J, Antonarakis S, Pericak-Vance MA.

Int J Neurol. 1991-1992;25-26:60-9. Review.

PMID:
11980064
9.

Familial amyotrophic lateral sclerosis with a novel G85S mutation of superoxide dismutase 1 gene: clinical features of lower motor neuron disease.

Takazawa T, Ikeda K, Hirayama T, Kawabe K, Nakamura Y, Ito H, Kano O, Yoshii Y, Tanaka F, Sobue G, Iwasaki Y.

Intern Med. 2010;49(2):183-6. Epub 2010 Jan 15.

10.

Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis.

Luigetti M, Conte A, Madia F, Marangi G, Zollino M, Mancuso I, Dileone M, Del Grande A, Di Lazzaro V, Tonali PA, Sabatelli M.

Neurol Sci. 2009 Dec;30(6):517-20. doi: 10.1007/s10072-009-0125-8. Epub 2009 Aug 15.

PMID:
19685200
11.

Progressive muscular atrophy variant of familial amyotrophic lateral sclerosis (PMA/ALS).

Cervenakova L, Protas II, Hirano A, Votiakov VI, Nedzved MK, Kolomiets ND, Taller I, Park KY, Sambuughin N, Gajdusek DC, Brown P, Goldfarb LG.

J Neurol Sci. 2000 Aug 15;177(2):124-30.

PMID:
10980308
12.

Positive effect of transplantation of hNT neurons (NTera 2/D1 cell-line) in a model of familial amyotrophic lateral sclerosis.

Garbuzova-Davis S, Willing AE, Milliken M, Saporta S, Zigova T, Cahill DW, Sanberg PR.

Exp Neurol. 2002 Apr;174(2):169-80. Erratum in: Exp Neurol 2002 Jun;175(2):451.

PMID:
11922659
13.

Onuf's nucleus is frequently involved in motor neuron disease/amyotrophic lateral sclerosis.

Bergmann M, Völpel M, Kuchelmeister K.

J Neurol Sci. 1995 Apr;129(2):141-6.

PMID:
7608728
14.

[From gene to disease: amyotrophic lateral sclerosis].

van Vught PW, Veldink JH, Baas F, van Muiswinkel FL, van den Berg LH.

Ned Tijdschr Geneeskd. 2004 Oct 23;148(43):2125-7. Review. Dutch.

PMID:
15553356
15.

Amyotrophic lateral sclerosis.

Wijesekera LC, Leigh PN.

Orphanet J Rare Dis. 2009 Feb 3;4:3. doi: 10.1186/1750-1172-4-3. Review.

16.
17.

Redox system expression in the motor neurons in amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS, superoxide dismutase 1 (SOD1)-mutated familial ALS, and SOD1-mutated ALS animal models.

Kato S, Kato M, Abe Y, Matsumura T, Nishino T, Aoki M, Itoyama Y, Asayama K, Awaya A, Hirano A, Ohama E.

Acta Neuropathol. 2005 Aug;110(2):101-12. Epub 2005 Jun 28.

PMID:
15983830
18.

Mutational analysis of the Cu/Zn superoxide dismutase gene in 23 familial and 69 sporadic cases of amyotrophic lateral sclerosis in Belgium.

Aguirre T, Matthijs G, Robberecht W, Tilkin P, Cassiman JJ.

Eur J Hum Genet. 1999 Jul;7(5):599-602.

19.

Amyotrophic lateral sclerosis: pathogenesis.

Brown RH Jr, Robberecht W.

Semin Neurol. 2001 Jun;21(2):131-9. Review.

PMID:
11442322
20.

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
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