85 related articles for article (PubMed ID: 18228570)
1. Marked diurnal fluctuation and rest benefit in a patient with parkin mutation.
Chung SJ; Park HK; Ki CS; Kim MJ; Lee MC
Mov Disord; 2008 Mar; 23(4):624-6. PubMed ID: 18228570
[No Abstract] [Full Text] [Related]
2. Dopamine dysregulation syndrome in a patient with early onset Parkinsonism and Parkin gene mutations.
Sammler EM; Swingler RJ; Stuart A; Muqit M
Mov Disord; 2009 Dec; 24(16):2442-3. PubMed ID: 19891003
[No Abstract] [Full Text] [Related]
3. Nigrostriatal dysfunction in patients with amyotrophic lateral sclerosis and parkinsonism.
Park HK; Lim YM; Kim JS; Lee MC; Kim SM; Kim BJ; Kim KK
J Neurol Sci; 2011 Feb; 301(1-2):12-3. PubMed ID: 21167502
[TBL] [Abstract][Full Text] [Related]
4. Decades of delayed diagnosis in 4 levodopa-responsive young-onset monogenetic parkinsonism patients.
Ling H; Braschinsky M; Taba P; Lüüs SM; Doherty K; Hotter A; Poewe W; Lees AJ
Mov Disord; 2011 Jun; 26(7):1337-40. PubMed ID: 21449012
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Parkin-related disease clinically diagnosed as a pallido-pyramidal syndrome.
Wickremaratchi MM; Majounie E; Morris HR; Williams NM; Lewis H; Gill SS; Khan S; Heywood P; Hardy J; Wiles CM; Singleton AB; Quinn NP
Mov Disord; 2009 Jan; 24(1):138-40. PubMed ID: 18942080
[No Abstract] [Full Text] [Related]
7. 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]
8. Parkinsonism and essential tremor in a family with pseudo-dominant inheritance of PARK2: an FP-CIT SPECT study.
Pellecchia MT; Varrone A; Annesi G; Amboni M; Cicarelli G; Sansone V; Annesi F; Rocca FE; Vitale C; Pappatà S; Quattrone A; Barone P
Mov Disord; 2007 Mar; 22(4):559-63. PubMed ID: 17149727
[TBL] [Abstract][Full Text] [Related]
9. Dopa-responsive parkinsonism phenotype of spinocerebellar ataxia type 2.
Lu CS; Wu Chou YH; Yen TC; Tsai CH; Chen RS; Chang HC
Mov Disord; 2002 Sep; 17(5):1046-51. PubMed ID: 12360557
[TBL] [Abstract][Full Text] [Related]
10. SPG7 with parkinsonism responsive to levodopa and dopaminergic deficit.
Pedroso JL; Vale TC; Bueno FL; Marussi VHR; Amaral LLFD; França MC; Barsottini OG
Parkinsonism Relat Disord; 2018 Feb; 47():88-90. PubMed ID: 29246844
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Clinical Reasoning: A demure teenager and her dystonic foot.
Cullinane PW; Browne P; Hennessy MJ; Counihan TJ
Neurology; 2017 Aug; 89(7):e71-e75. PubMed ID: 28808173
[No Abstract] [Full Text] [Related]
14. Different cerebral cortical areas influence the effect of subthalamic nucleus stimulation on parkinsonian motor deficits and freezing of gait.
Lyoo CH; Aalto S; Rinne JO; Lee KO; Oh SH; Chang JW; Lee MS
Mov Disord; 2007 Nov; 22(15):2176-82. PubMed ID: 17712844
[TBL] [Abstract][Full Text] [Related]
15. Autosomal recessive juvenile parkinsonism Cys212Tyr mutation in parkin renders lymphocytes susceptible to dopamine- and iron-mediated apoptosis.
Jimenez Del Rio M; Moreno S; Garcia-Ospina G; Buritica O; Uribe CS; Lopera F; Velez-Pardo C
Mov Disord; 2004 Mar; 19(3):324-30. PubMed ID: 15022188
[TBL] [Abstract][Full Text] [Related]
16. Clinical and genetic studies on familial parkinsonism: the first report on a parkin gene mutation in a Taiwanese family.
Lu CS; Wu JC; Tsai CH; Chen RS; Chou YH; Hattori N; Yoshino H; Mizuno Y
Mov Disord; 2001 Jan; 16(1):164-6. PubMed ID: 11215581
[No Abstract] [Full Text] [Related]
17. 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]
18. Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease.
Quattrone A; Bagnato A; Annesi G; Novellino F; Morgante L; Savettieri G; Zappia M; Tarantino P; Candiano IC; Annesi F; Civitelli D; Rocca FE; D'Amelio M; Nicoletti G; Morelli M; Petrone A; Loizzo P; Condino F
Mov Disord; 2008 Jan; 23(1):21-7. PubMed ID: 17975812
[TBL] [Abstract][Full Text] [Related]
19. Biallelic Parkin (PARK2) mutations can cause a bvFTD phenotype without clinically relevant parkinsonism.
Zimmermann M; Wilke C; Schulte C; Hoffmann J; Klopfer J; Reimold M; Brockmann K; Synofzik M
Parkinsonism Relat Disord; 2018 Oct; 55():145-147. PubMed ID: 29910155
[No Abstract] [Full Text] [Related]
20. Roll on genetics of PARK and Parkinsonism in the developing world.
Kalaria RN; Akinyemi R
J Neurol Neurosurg Psychiatry; 2010 Feb; 81(2):128. PubMed ID: 20145023
[No Abstract] [Full Text] [Related]
[Next] [New Search]