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Results: 1 to 20 of 108

1.

Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent dataset.

Bonifati V, Breedveld GJ, Squitieri F, Vanacore N, Brustenghi P, Harhangi BS, Montagna P, Cannella M, Fabbrini G, Rizzu P, van Duijn CM, Oostra BA, Meco G, Heutink P.

Ann Neurol. 2002 Feb;51(2):253-6.

PMID:
11835383
[PubMed - indexed for MEDLINE]
2.

Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36.

van Duijn CM, Dekker MC, Bonifati V, Galjaard RJ, Houwing-Duistermaat JJ, Snijders PJ, Testers L, Breedveld GJ, Horstink M, Sandkuijl LA, van Swieten JC, Oostra BA, Heutink P.

Am J Hum Genet. 2001 Sep;69(3):629-34. Epub 2001 Jul 2.

PMID:
11462174
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7.

Bonifati V, Dekker MC, Vanacore N, Fabbrini G, Squitieri F, Marconi R, Antonini A, Brustenghi P, Dalla Libera A, De Mari M, Stocchi F, Montagna P, Gallai V, Rizzu P, van Swieten JC, Oostra B, van Duijn CM, Meco G, Heutink P; Italian Parkinson Genetics Network.

Neurol Sci. 2002 Sep;23 Suppl 2:S59-60.

PMID:
12548343
[PubMed - indexed for MEDLINE]
4.

Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36.

Valente EM, Bentivoglio AR, Dixon PH, Ferraris A, Ialongo T, Frontali M, Albanese A, Wood NW.

Am J Hum Genet. 2001 Apr;68(4):895-900. Epub 2001 Mar 7.

PMID:
11254447
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

PARK6 is a common cause of familial parkinsonism.

Valente EM, Brancati F, Caputo V, Graham EA, Davis MB, Ferraris A, Breteler MM, Gasser T, Bonifati V, Bentivoglio AR, De Michele G, Dürr A, Cortelli P, Filla A, Meco G, Oostra BA, Brice A, Albanese A, Dallapiccola B, Wood NW; European Consortium on Genetic Susceptibility in Parkinson's Disease.

Neurol Sci. 2002 Sep;23 Suppl 2:S117-8.

PMID:
12548371
[PubMed - indexed for MEDLINE]
6.

DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism.

Bonifati V, Rizzu P, Squitieri F, Krieger E, Vanacore N, van Swieten JC, Brice A, van Duijn CM, Oostra B, Meco G, Heutink P.

Neurol Sci. 2003 Oct;24(3):159-60.

PMID:
14598065
[PubMed - indexed for MEDLINE]
7.

Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism.

Ibáñez P, De Michele G, Bonifati V, Lohmann E, Thobois S, Pollak P, Agid Y, Heutink P, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group.

Neurology. 2003 Nov 25;61(10):1429-31.

PMID:
14638971
[PubMed - indexed for MEDLINE]
8.

Homozygous exon 4 deletion in parkin gene in a Korean family with autosomal recessive early onset parkinsonism.

Kim JS, Lee KS, Kim YI, Lee KH, Kim HT.

Yonsei Med J. 2003 Apr 30;44(2):336-9.

PMID:
12728478
[PubMed - indexed for MEDLINE]
Free Article
9.

Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype.

Klein C, Pramstaller PP, Kis B, Page CC, Kann M, Leung J, Woodward H, Castellan CC, Scherer M, Vieregge P, Breakefield XO, Kramer PL, Ozelius LJ.

Ann Neurol. 2000 Jul;48(1):65-71.

PMID:
10894217
[PubMed - indexed for MEDLINE]
10.

Clinical features and neuroimaging of PARK7-linked parkinsonism.

Dekker M, Bonifati V, van Swieten J, Leenders N, Galjaard RJ, Snijders P, Horstink M, Heutink P, Oostra B, van Duijn C.

Mov Disord. 2003 Jul;18(7):751-7.

PMID:
12815653
[PubMed - indexed for MEDLINE]
11.

Parkin gene causing benign autosomal recessive juvenile parkinsonism.

Nisipeanu P, Inzelberg R, Abo Mouch S, Carasso RL, Blumen SC, Zhang J, Matsumine H, Hattori N, Mizuno Y.

Neurology. 2001 Jun 12;56(11):1573-5.

PMID:
11402119
[PubMed - indexed for MEDLINE]
12.

PARK6-linked parkinsonism occurs in several European families.

Valente EM, Brancati F, Ferraris A, Graham EA, Davis MB, Breteler MM, Gasser T, Bonifati V, Bentivoglio AR, De Michele G, Dürr A, Cortelli P, Wassilowsky D, Harhangi BS, Rawal N, Caputo V, Filla A, Meco G, Oostra BA, Brice A, Albanese A, Dallapiccola B, Wood NW; European Consortium on Genetic Susceptibility in Parkinson's Disease.

Ann Neurol. 2002 Jan;51(1):14-8.

PMID:
11782979
[PubMed - indexed for MEDLINE]
13.

Parkin mutations are frequent in patients with isolated early-onset parkinsonism.

Periquet M, Latouche M, Lohmann E, Rawal N, De Michele G, Ricard S, Teive H, Fraix V, Vidailhet M, Nicholl D, Barone P, Wood NW, Raskin S, Deleuze JF, Agid Y, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease.

Brain. 2003 Jun;126(Pt 6):1271-8.

PMID:
12764050
[PubMed - indexed for MEDLINE]
Free Article
14.

Relative high frequency of the c.255delA parkin gene mutation in Spanish patients with autosomal recessive parkinsonism.

Muñoz E, Tolosa E, Pastor P, Martí MJ, Valldeoriola F, Campdelacreu J, Oliva R.

J Neurol Neurosurg Psychiatry. 2002 Nov;73(5):582-4.

PMID:
12397156
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Phenotypic characterisation of autosomal recessive PARK6-linked parkinsonism in three unrelated Italian families.

Bentivoglio AR, Cortelli P, Valente EM, Ialongo T, Ferraris A, Elia A, Montagna P, Albanese A.

Mov Disord. 2001 Nov;16(6):999-1006.

PMID:
11748730
[PubMed - indexed for MEDLINE]
16.

Autosomal-recessive juvenile parkinsonism in a Jewish Yemenite kindred: mutation of Parkin gene.

Nisipeanu P, Inzelberg R, Blumen SC, Carasso RL, Hattori N, Matsumine H, Mizuno Y.

Neurology. 1999 Oct 22;53(7):1602-4.

PMID:
10534280
[PubMed - indexed for MEDLINE]
17.

Pseudo-autosomal dominant inheritance of PARK2: two families with parkin gene mutations.

Kobayashi T, Matsumine H, Zhang J, Imamichi Y, Mizuno Y, Hattori N.

J Neurol Sci. 2003 Mar 15;207(1-2):11-7.

PMID:
12614925
[PubMed - indexed for MEDLINE]
18.

Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism.

Bonifati V, Lücking CB, Fabrizio E, Periquet M, Meco G, Brice A.

J Neurol Neurosurg Psychiatry. 2001 Oct;71(4):531-4.

PMID:
11561042
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Autosomal recessive juvenile parkinsonism.

Saito M, Maruyama M, Ikeuchi K, Kondo H, Ishikawa A, Yuasa T, Tsuji S.

Brain Dev. 2000 Sep;22 Suppl 1:S115-7. Review.

PMID:
10984671
[PubMed - indexed for MEDLINE]
20.

Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism.

Maruyama M, Ikeuchi T, Saito M, Ishikawa A, Yuasa T, Tanaka H, Hayashi S, Wakabayashi K, Takahashi H, Tsuji S.

Ann Neurol. 2000 Aug;48(2):245-50.

PMID:
10939576
[PubMed - indexed for MEDLINE]

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