126 related articles for article (PubMed ID: 15641013)
1. Parkin disease in a Brazilian kindred: Manifesting heterozygotes and clinical follow-up over 10 years.
Khan NL; Horta W; Eunson L; Graham E; Johnson JO; Chang S; Davis M; Singleton A; Wood NW; Lees AJ
Mov Disord; 2005 Apr; 20(4):479-484. PubMed ID: 15641013
[TBL] [Abstract][Full Text] [Related]
2. 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
Mov Disord; 2003 Aug; 18(8):914-9. PubMed ID: 12889082
[TBL] [Abstract][Full Text] [Related]
3. Chronic bilateral subthalamic deep brain stimulation in a patient with homozygous deletion in the parkin gene.
Capecci M; Passamonti L; Annesi F; Annesi G; Bellesi M; Candiano IC; Ricciuti R; Iacoangeli M; Scerrati M; Zappia M; Tarantino P; De Marco EV; Civitelli D; Carrideo S; Provinciali L; Ceravolo MG; Quattrone A
Mov Disord; 2004 Dec; 19(12):1450-2. PubMed ID: 15390056
[TBL] [Abstract][Full Text] [Related]
4. Are parkin patients particularly suited for deep-brain stimulation?
Lohmann E; Welter ML; Fraix V; Krack P; Lesage S; Laine S; Tanguy ML; Houeto JL; Mesnage V; Pollak P; Durr A; Agid Y; Brice A;
Mov Disord; 2008 Apr; 23(5):740-3. PubMed ID: 18228569
[TBL] [Abstract][Full Text] [Related]
5. Pseudo-orthostatic and resting leg tremor in a large Spanish family with homozygous truncating parkin mutation.
Infante J; Berciano J; Sánchez-Juan P; García A; Di Fonzo A; Breedveld G; Oostra B; Bonifati V
Mov Disord; 2009 Jan; 24(1):144-7. PubMed ID: 18951541
[No Abstract] [Full Text] [Related]
6. Amantadine for levodopa-induced choreic dyskinesia in compound heterozygotes for GCH1 mutations.
Furukawa Y; Filiano JJ; Kish SJ
Mov Disord; 2004 Oct; 19(10):1256-8. PubMed ID: 15389992
[TBL] [Abstract][Full Text] [Related]
7. Clinical findings in a large family with a parkin ex3delta40 mutation.
Munhoz RP; Sa DS; Rogaeva E; Salehi-Rad S; Sato C; Medeiros H; Farrer M; Lang AE
Arch Neurol; 2004 May; 61(5):701-4. PubMed ID: 15148147
[TBL] [Abstract][Full Text] [Related]
8. 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
BMC Neurol; 2008 Dec; 8():47. PubMed ID: 19087301
[TBL] [Abstract][Full Text] [Related]
9. Parkin mutations and early-onset parkinsonism in a Taiwanese cohort.
Wu RM; Bounds R; Lincoln S; Hulihan M; Lin CH; Hwu WL; Chen J; Gwinn-Hardy K; Farrer M
Arch Neurol; 2005 Jan; 62(1):82-7. PubMed ID: 15642853
[TBL] [Abstract][Full Text] [Related]
10. Marked variation in clinical presentation and age of onset in a family with a heterozygous parkin mutation.
Tan LC; Tanner CM; Chen R; Chan P; Farrer M; Hardy J; Langston JW
Mov Disord; 2003 Jul; 18(7):758-63. PubMed ID: 12815654
[TBL] [Abstract][Full Text] [Related]
11. The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
Bonifati V; De Michele G; Lücking CB; Dürr A; Fabrizio E; Ambrosio G; Vanacore N; De Mari M; Marconi R; Capus L; Breteler MM; Gasser T; Oostra B; Wood N; Agid Y; Filla A; Meco G; Brice A;
Neurol Sci; 2001 Feb; 22(1):51-2. PubMed ID: 11487197
[TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 11561042
[TBL] [Abstract][Full Text] [Related]
13. How much phenotypic variation can be attributed to parkin genotype?
Lohmann E; Periquet M; Bonifati V; Wood NW; De Michele G; Bonnet AM; Fraix V; Broussolle E; Horstink MW; Vidailhet M; Verpillat P; Gasser T; Nicholl D; Teive H; Raskin S; Rascol O; Destée A; Ruberg M; Gasparini F; Meco G; Agid Y; Durr A; Brice A; ;
Ann Neurol; 2003 Aug; 54(2):176-85. PubMed ID: 12891670
[TBL] [Abstract][Full Text] [Related]
14. Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study.
Gouider-Khouja N; Larnaout A; Amouri R; Sfar S; Belal S; Ben Hamida C; Ben Hamida M; Hattori N; Mizuno Y; Hentati F
Parkinsonism Relat Disord; 2003 Jun; 9(5):247-51. PubMed ID: 12781588
[TBL] [Abstract][Full Text] [Related]
15. 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; ;
N Engl J Med; 2000 May; 342(21):1560-7. PubMed ID: 10824074
[TBL] [Abstract][Full Text] [Related]
16. Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations.
Lücking CB; Bonifati V; Periquet M; Vanacore N; Brice A; Meco G
Neurology; 2001 Sep; 57(5):924-7. PubMed ID: 11552035
[TBL] [Abstract][Full Text] [Related]
17. Detection of compound heterozygous deletions in the parkin gene of fibroblasts in patients with autosomal recessive hereditary parkinsonism (PARK2).
Nakaso K; Adachi Y; Yasui K; Sakuma K; Nakashima K
Neurosci Lett; 2006 May; 400(1-2):44-7. PubMed ID: 16517073
[TBL] [Abstract][Full Text] [Related]
18. Parkin disease: a phenotypic study of a large case series.
Khan NL; Graham E; Critchley P; Schrag AE; Wood NW; Lees AJ; Bhatia KP; Quinn N
Brain; 2003 Jun; 126(Pt 6):1279-92. PubMed ID: 12764051
[TBL] [Abstract][Full Text] [Related]
19. 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. PubMed ID: 10894217
[TBL] [Abstract][Full Text] [Related]
20. LRRK2 and Parkin mutations in a family with parkinsonism-Lack of genotype-phenotype correlation.
Marras C; Klein C; Lang AE; Wakutani Y; Moreno D; Sato C; Yip E; Munhoz RP; Lohmann K; Djarmati A; Bi A; Rogaeva E
Neurobiol Aging; 2010 Apr; 31(4):721-2. PubMed ID: 18644660
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]