Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 72

1.

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.

Hum Mol Genet. 1999 Apr;8(4):567-74.

PMID:
10072423
2.

[Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease].

Hattori N.

Rinsho Shinkeigaku. 2004 Apr-May;44(4-5):241-62. Review. Japanese.

PMID:
15287506
3.

Autosomal recessive juvenile parkinsonism: a key to understanding nigral degeneration in sporadic Parkinson's disease.

Hattori N, Shimura H, Kubo S, Kitada T, Wang M, Asakawa S, Minashima S, Shimizu N, Suzuki T, Tanaka K, Mizuno Y.

Neuropathology. 2000 Sep;20 Suppl:S85-90. Review.

PMID:
11037196
4.

Genetics of Parkinson's disease.

Polymeropoulos MH.

Ann N Y Acad Sci. 2000;920:28-32. Review.

PMID:
11193165
5.

Parkin-associated Parkinson's disease.

von Coelln R, Dawson VL, Dawson TM.

Cell Tissue Res. 2004 Oct;318(1):175-84. Epub 2004 Jul 30. Review.

PMID:
15503153
6.

[Molecular genetics of PINK1].

Funayama M, Hattori N.

Brain Nerve. 2007 Aug;59(8):831-8. Review. Japanese.

PMID:
17713119
7.

Distribution, type, and origin of Parkin mutations: review and case studies.

Hedrich K, Eskelson C, Wilmot B, Marder K, Harris J, Garrels J, Meija-Santana H, Vieregge P, Jacobs H, Bressman SB, Lang AE, Kann M, Abbruzzese G, Martinelli P, Schwinger E, Ozelius LJ, Pramstaller PP, Klein C, Kramer P.

Mov Disord. 2004 Oct;19(10):1146-57. Review.

PMID:
15390068
8.

PARKIN as a pathogenic gene for autosomal recessive juvenile parkinsonism.

Shimizu N, Asakawa S, Minoshima S, Kitada T, Hattori N, Matsumine H, Yokochi M, Yamamura Y, Mizuno Y.

J Neural Transm Suppl. 2000;(58):19-30. Review.

PMID:
11128608
9.

Parkin and Parkinson's disease.

Mizuno Y, Hattori N, Mori H, Suzuki T, Tanaka K.

Curr Opin Neurol. 2001 Aug;14(4):477-82. Review.

PMID:
11470964
10.

Update on the genetics of Parkinson's disease.

Gasser T.

Mov Disord. 2007 Sep;22 Suppl 17:S343-50. doi: 10.1002/mds.21676. Review.

PMID:
18175395
11.

Diagnostic considerations in juvenile parkinsonism.

Paviour DC, Surtees RA, Lees AJ.

Mov Disord. 2004 Feb;19(2):123-35. Review.

PMID:
14978667
12.

Parkin genetics: one model for Parkinson's disease.

Mata IF, Lockhart PJ, Farrer MJ.

Hum Mol Genet. 2004 Apr 1;13 Spec No 1:R127-33. Epub 2004 Feb 19. Review.

PMID:
14976155
13.

[Parkin gene: its mutations and function].

Hattori N.

Rinsho Shinkeigaku. 2002 Nov;42(11):1077-81. Review. Japanese.

PMID:
12784670
14.

[Parkin, alpha-synuclein and other molecular aspects of Parkinson's disease].

Corti O, Brice A.

J Soc Biol. 2002;196(1):95-10. Review. French.

PMID:
12134640
15.

Progress in the clinical and molecular genetics of familial parkinsonism.

Kitada T, Asakawa S, Matsumine H, Hattori N, Shimura H, Minoshima S, Shimizu N, Mizuno Y.

Neurogenetics. 2000 Mar;2(4):207-18. Review.

PMID:
10983716
16.

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
17.

Genetics of Parkinson's disease.

Gasser T.

J Neurol. 2001 Oct;248(10):833-40. Review.

PMID:
11697518
18.

[Genetics of Parkinson disease].

Brassat D, Durr A, Agid Y, Brice A.

Rev Med Interne. 1999 Aug;20(8):709-14. Review. French.

PMID:
10480176
19.

Genetics of Parkinson's disease.

Mizuno Y, Hattori N, Mori H.

Biomed Pharmacother. 1999 Apr;53(3):109-16. Review.

PMID:
10349506
20.

Parkin is linked to the ubiquitin pathway.

Tanaka K, Suzuki T, Chiba T, Shimura H, Hattori N, Mizuno Y.

J Mol Med (Berl). 2001 Sep;79(9):482-94. Review.

PMID:
11692161

Supplemental Content

Support Center