Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 62

1.

No association between genetic polymorphism at codon 129 of the prion protein gene and primary progressive multiple sclerosis.

Stüve O, Wang J, Chan A, Hemmer B, Cepok S, Nessler S, Zipp F, Goldman MD, Meuth SG, Korth C, Lambracht-Washington D.

Arch Neurol. 2011 Feb;68(2):264-5. doi: 10.1001/archneurol.2010.354. No abstract available. Erratum in: Arch Neurol. 2011 Mar;68(3):302.

PMID:
21320996
2.

Genetic association of CASP8 polymorphisms with primary progressive multiple sclerosis.

Camiña-Tato M, Fernández M, Morcillo-Suárez C, Navarro A, Julià E, Edo MC, Montalban X, Comabella M.

J Neuroimmunol. 2010 May;222(1-2):70-5. doi: 10.1016/j.jneuroim.2010.03.003. Epub 2010 Apr 2.

PMID:
20363033
3.

Evidence for association of chromosome 10 open reading frame (C10orf27) gene polymorphisms and multiple sclerosis.

Goertsches R, Baranzini SE, Morcillo C, Nos C, Camiña M, Oksenberg JR, Montalban X, Comabella M.

Mult Scler. 2008 Apr;14(3):412-4. doi: 10.1177/1352458507083780. Epub 2008 Jan 21.

PMID:
18208870
4.

Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease.

Mead S, Beck J, Dickinson A, Fisher EM, Collinge J.

Neurosci Lett. 2000 Aug 25;290(2):117-20.

PMID:
10936691
5.

The genetic influence of the nonclassical MHC molecule HLA-G on multiple sclerosis.

Kroner A, Grimm A, Johannssen K, Mäurer M, Wiendl H.

Hum Immunol. 2007 May;68(5):422-5. Epub 2007 Feb 15.

PMID:
17462509
6.

Tumour necrosis factor alpha gene (TNF-alpha) -376 polymorphism in Hungarian patients with primary progressive multiple sclerosis.

Losonczi E, Bencsik K, Nagy ZF, Honti V, Szalczer E, Rajda C, Illés Z, Mátyás K, Rózsa C, Csépány T, Füvesi J, Vécsei L.

J Neuroimmunol. 2009 Mar 31;208(1-2):115-8. doi: 10.1016/j.jneuroim.2009.01.004. Epub 2009 Feb 6.

PMID:
19201038
7.

APOE epsilon status in Hungarian patients with primary progressive multiple sclerosis.

Losonczi E, Bencsik K, Fricska Nagy Z, Honti V, Szalczer E, Rajda C, Illés Z, Mátyás K, Rózsa C, Csépány T, Füvesi J, Vécsei L.

Swiss Med Wkly. 2010 Nov 26;140:w13119. doi: 10.4414/smw.2010.13119.

8.

Comment to Tumour necrosis factor alpha gene -376 polymorphism in Hungarian patients with primary progressive multiple sclerosis.

Kauffman MA, Villa AM.

J Neuroimmunol. 2009 Jul 25;212(1-2):151. doi: 10.1016/j.jneuroim.2009.05.001. Epub 2009 May 15. No abstract available.

PMID:
19446891
9.

Prion protein codon 129 genotype prevalence is altered in primary progressive aphasia.

Li X, Rowland LP, Mitsumoto H, Przedborski S, Bird TD, Schellenberg GD, Peskind E, Johnson N, Siddique T, Mesulam MM, Weintraub S, Mastrianni JA.

Ann Neurol. 2005 Dec;58(6):858-64.

PMID:
16315279
10.

Interleukin 18 receptor 1 expression distinguishes patients with multiple sclerosis.

Gillett A, Thessen Hedreul M, Khademi M, Espinosa A, Beyeen AD, Jagodic M, Kockum I, Harris RA, Olsson T.

Mult Scler. 2010 Sep;16(9):1056-65. doi: 10.1177/1352458510364634. Epub 2010 Mar 30.

PMID:
20354066
11.

Frequency of functional interleukin-10 promoter polymorphism is different between relapse-onset and primary progressive multiple sclerosis.

de Jong BA, Westendorp RG, Eskdale J, Uitdehaag BM, Huizinga TW.

Hum Immunol. 2002 Apr;63(4):281-5.

PMID:
12039409
12.

Lack of evidence to support the association of the human prion gene with schizophrenia.

Tsai MT, Su YC, Chen YH, Chen CH.

Mol Psychiatry. 2001 Jan;6(1):74-8.

PMID:
11244488
13.

Polymorphism at 3' UTR +28 of the prion-like protein gene is associated with sporadic Creutzfeldt-Jakob disease.

Jeong BH, Kim NH, Choi EK, Lee C, Song YH, Kim JI, Carp RI, Kim YS.

Eur J Hum Genet. 2005 Sep;13(9):1094-7.

14.

The human prion gene M129V polymorphism is not associated with idiopathic Parkinson's disease in three distinct populations.

Scholz SW, Xiromerisiou G, Fung HC, Eerola J, Hellström O, Papadimitriou A, Hadjigeorgiou GM, Tienari PJ, Fernandez HH, Mandel R, Okun MS, Gwinn-Hardy K, Singleton AB.

Neurosci Lett. 2006 Mar 13;395(3):227-9. Epub 2005 Nov 18.

PMID:
16298483
15.

Prion disease genetics.

Mead S.

Eur J Hum Genet. 2006 Mar;14(3):273-81. Review.

16.
17.

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism.

Goldfarb LG, Petersen RB, Tabaton M, Brown P, LeBlanc AC, Montagna P, Cortelli P, Julien J, Vital C, Pendelbury WW, et al.

Science. 1992 Oct 30;258(5083):806-8.

PMID:
1439789
18.

Does the prion protein gene 129 codon polymorphism influence sleep? Evidence from a fatal familial insomnia kindred.

Plazzi G, Montagna P, Beelke M, Nobili L, De Carli F, Cortelli P, Vandi S, Avoni P, Tinuper P, Gambetti P, Lugaresi E, Ferrillo F.

Clin Neurophysiol. 2002 Dec;113(12):1948-53.

PMID:
12464332
19.

Interleukin-10 promoter polymorphisms in patients with multiple sclerosis.

Myhr KM, Vågnes KS, Marøy TH, Aarseth JH, Nyland HI, Vedeler CA.

J Neurol Sci. 2002 Oct 15;202(1-2):93-7.

PMID:
12220699
20.

A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease.

Yamada M, Itoh Y, Fujigasaki H, Naruse S, Kaneko K, Kitamoto T, Tateishi J, Otomo E, Hayakawa M, Tanaka J, et al.

Neurology. 1993 Dec;43(12):2723-4. No abstract available.

PMID:
7902972

Supplemental Content

Support Center