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Items: 15

1.

A novel form of juvenile recessive ALS maps to loci on 6p25 and 21q22.

Butterfield RJ, Ramachandran D, Hasstedt SJ, Otterud BE, Leppert MF, Swoboda KJ, Flanigan KM.

Neuromuscul Disord. 2009 Apr;19(4):279-87. doi: 10.1016/j.nmd.2009.02.006. Epub 2009 Mar 21.

PMID:
19318250
2.

Genetic factors in the early diagnosis of ALS.

Andersen PM.

Amyotroph Lateral Scler Other Motor Neuron Disord. 2000 Mar;1 Suppl 1:S31-42. Review.

PMID:
11464924
3.

[Juvenile and adult forms of spinal muscular atrophies].

Pou A.

Neurologia. 1996 Dec;11 Suppl 5:43-57. Review. Spanish.

PMID:
9044573
4.

Molecular and cellular function of ALS2/alsin: implication of membrane dynamics in neuronal development and degeneration.

Hadano S, Kunita R, Otomo A, Suzuki-Utsunomiya K, Ikeda JE.

Neurochem Int. 2007 Jul-Sep;51(2-4):74-84. Epub 2007 May 4. Review.

PMID:
17566607
5.
6.

Primary lateral sclerosis.

Singer MA, Statland JM, Wolfe GI, Barohn RJ.

Muscle Nerve. 2007 Mar;35(3):291-302. Review.

PMID:
17212349
7.

[Primary lateral sclerosis: the era of international diagnosis criteria].

Le Forestier N, Meininger V.

Rev Neurol (Paris). 2009 May;165(5):415-29. doi: 10.1016/j.neurol.2008.07.022. Epub 2008 Oct 7. Review. French.

PMID:
18842276
8.

Mutations in PEX10 are a cause of autosomal recessive ataxia.

Régal L, Ebberink MS, Goemans N, Wanders RJ, De Meirleir L, Jaeken J, Schrooten M, Van Coster R, Waterham HR.

Ann Neurol. 2010 Aug;68(2):259-63. doi: 10.1002/ana.22035. Review.

PMID:
20695019
9.

Axon guidance proteins: novel therapeutic targets for ALS?

Schmidt ER, Pasterkamp RJ, van den Berg LH.

Prog Neurobiol. 2009 Aug;88(4):286-301. doi: 10.1016/j.pneurobio.2009.05.004. Epub 2009 Jun 10. Review.

PMID:
19523502
10.

The monogenic primary dystonias.

Müller U.

Brain. 2009 Aug;132(Pt 8):2005-25. doi: 10.1093/brain/awp172. Epub 2009 Jul 3. Review.

PMID:
19578124
11.

The management of amyotrophic lateral sclerosis.

Phukan J, Hardiman O.

J Neurol. 2009 Feb;256(2):176-86. doi: 10.1007/s00415-009-0142-9. Epub 2009 Feb 17. Review.

PMID:
19224316
12.

The complex relation between genotype and phenotype in motor neuron disease.

Cañete-Soler R, Schlaepfer WW.

Ann Neurol. 2007 Jul;62(1):8-14. Review.

PMID:
17469207
13.

The genetic heterogeneity of mendelian susceptibility to mycobacterial diseases.

Al-Muhsen S, Casanova JL.

J Allergy Clin Immunol. 2008 Dec;122(6):1043-51; quiz 1052-3. doi: 10.1016/j.jaci.2008.10.037. Review.

PMID:
19084105
14.

[Juvenile ALS].

Warita H, Abe K.

Ryoikibetsu Shokogun Shirizu. 1999;(27 Pt 2):323-5. Review. Japanese. No abstract available.

PMID:
10434664
15.

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