Similar articles for PMID: 10939576

Year	Number of Results
1996	1
1998	3
1999	2
2000	11
2001	12
2002	8
2003	9
2004	5
2005	8
2006	3
2007	5
2008	4
2009	9
2010	3
2011	7
2012	4
2013	1
2014	3
2015	4
2016	7
2017	7
2018	8
2019	3
2020	7
2021	3
2022	1
2023	2
2024	2

1

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. Maruyama M, et al. Ann Neurol. 2000 Aug;48(2):245-50. Ann Neurol. 2000. PMID: 10939576

2

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. Nisipeanu P, et al. Neurology. 2001 Jun 12;56(11):1573-5. doi: 10.1212/wnl.56.11.1573. Neurology. 2001. PMID: 11402119

3

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.

Abbas N, Lücking CB, Ricard S, Dürr A, Bonifati V, De Michele G, Bouley S, Vaughan JR, Gasser T, Marconi R, Broussolle E, Brefel-Courbon C, Harhangi BS, Oostra BA, Fabrizio E, Böhme GA, Pradier L, Wood NW, Filla A, Meco G, Denefle P, Agid Y, Brice A. Abbas N, et al. Hum Mol Genet. 1999 Apr;8(4):567-74. doi: 10.1093/hmg/8.4.567. Hum Mol Genet. 1999. PMID: 10072423

4

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. Klein C, et al. Ann Neurol. 2000 Jul;48(1):65-71. Ann Neurol. 2000. PMID: 10894217

5

Homozygous partial genomic triplication of the parkin gene in early-onset parkinsonism.

Mata IF, Alvarez V, Coto E, Blazquez M, Guisasola LM, Salvador C, Kachergus JM, Lincoln SJ, Farrer M. Mata IF, et al. Neurosci Lett. 2005 Jun 3;380(3):257-9. doi: 10.1016/j.neulet.2005.01.051. Epub 2005 Feb 8. Neurosci Lett. 2005. PMID: 15862897

6

Significance of the parkin and PINK1 gene in Jordanian families with incidences of young-onset and juvenile parkinsonism.

Myhre R, Steinkjer S, Stormyr A, Nilsen GL, Abu Zayyad H, Horany K, Nusier MK, Klungland H. Myhre R, et al. BMC Neurol. 2008 Dec 16;8:47. doi: 10.1186/1471-2377-8-47. BMC Neurol. 2008. PMID: 19087301 Free PMC article.

7

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. Kim JS, et al. Yonsei Med J. 2003 Apr 30;44(2):336-9. doi: 10.3349/ymj.2003.44.2.336. Yonsei Med J. 2003. PMID: 12728478 Free article.

8

Clinicogenetic study of PINK1 mutations in autosomal recessive early-onset parkinsonism.

Li Y, Tomiyama H, Sato K, Hatano Y, Yoshino H, Atsumi M, Kitaguchi M, Sasaki S, Kawaguchi S, Miyajima H, Toda T, Mizuno Y, Hattori N. Li Y, et al. Neurology. 2005 Jun 14;64(11):1955-7. doi: 10.1212/01.WNL.0000164009.36740.4E. Neurology. 2005. PMID: 15955953

9

Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism.

Illarioshkin SN, Periquet M, Rawal N, Lücking CB, Zagorovskaya TB, Slominsky PA, Miloserdova OV, Markova ED, Limborska SA, Ivanova-Smolenskaya IA, Brice A. Illarioshkin SN, et al. Mov Disord. 2003 Aug;18(8):914-9. doi: 10.1002/mds.10467. Mov Disord. 2003. PMID: 12889082

10

Association between early-onset Parkinson's disease and mutations in the parkin gene.

Lücking CB, Dürr A, Bonifati V, Vaughan J, De Michele G, Gasser T, Harhangi BS, Meco G, Denèfle P, Wood NW, Agid Y, Brice A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. Lücking CB, et al. N Engl J Med. 2000 May 25;342(21):1560-7. doi: 10.1056/NEJM200005253422103. N Engl J Med. 2000. PMID: 10824074 Free article.

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