Literature DB >> 21221111

Parkinson disease: genetic testing in Parkinson disease-who should be assessed?

Christine Klein, Ana Djarmati.   

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Year:  2011        PMID: 21221111     DOI: 10.1038/nrneurol.2010.197

Source DB:  PubMed          Journal:  Nat Rev Neurol        ISSN: 1759-4758            Impact factor:   42.937


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  9 in total

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

Authors:  C B Lücking; A Dürr; V Bonifati; J Vaughan; G De Michele; T Gasser; B S Harhangi; G Meco; P Denèfle; N W Wood; Y Agid; A Brice
Journal:  N Engl J Med       Date:  2000-05-25       Impact factor: 91.245

2.  Genotypic and phenotypic characteristics of Dutch patients with early onset Parkinson's disease.

Authors:  Maria G Macedo; Dagmar Verbaan; Yue Fang; Stephanie M van Rooden; Martine Visser; Burcu Anar; Antonella Uras; Justus L Groen; Patrizia Rizzu; Jacobus J van Hilten; Peter Heutink
Journal:  Mov Disord       Date:  2009-01-30       Impact factor: 10.338

3.  Comparing knowledge and attitudes towards genetic testing in Parkinson's disease in an American and Asian population.

Authors:  Eng-King Tan; Jennie Lee; Christine Hunter; Lina Shinawi; S Fook-Chong; Joseph Jankovic
Journal:  J Neurol Sci       Date:  2006-12-14       Impact factor: 3.181

Review 4.  The genetics of Parkinson disease: Implications for neurological care.

Authors:  Christine Klein; Michael G Schlossmacher
Journal:  Nat Clin Pract Neurol       Date:  2006-03

5.  Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease study.

Authors:  Roy N Alcalay; Elise Caccappolo; Helen Mejia-Santana; Ming Xin Tang; Llency Rosado; Barbara M Ross; Miguel Verbitsky; Sergey Kisselev; Elan D Louis; Cynthia Comella; Amy Colcher; Danna Jennings; Martha A Nance; Susan B Bressman; William K Scott; Caroline Tanner; Susan Mickel; Howard Andrews; Cheryl Waters; Stanley Fahn; Lucien Cote; Steven Frucht; Blair Ford; Michael Rezak; Kevin Novak; Joseph H Friedman; Ronald Pfeiffer; Laura Marsh; Bradley Hiner; Andrew Siderowf; Ruth Ottman; Karen Marder; Lorraine N Clark
Journal:  Arch Neurol       Date:  2010-09

6.  Attitudes of young patients with Parkinson's disease towards possible presymptomatic and prenatal genetic testing.

Authors:  H Jacobs; U Latza; A Vieregge; P Vieregge
Journal:  Genet Couns       Date:  2001

7.  Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease.

Authors:  Jung Mi Choi; Myoung Soo Woo; Hyeo-Il Ma; Suk Yun Kang; Young-Hee Sung; Seok Woo Yong; Sun Ju Chung; Joong-Seok Kim; Hae-won Shin; Chul Hyoung Lyoo; Phil Hyu Lee; Jong Sam Baik; Sang-Jin Kim; Mee Young Park; Young Ho Sohn; Jin-Ho Kim; Jae Woo Kim; Myung Sik Lee; Myoung Chong Lee; Dong-Hyun Kim; Yun Joong Kim
Journal:  Neurogenetics       Date:  2008-08-15       Impact factor: 2.660

8.  Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population.

Authors:  Karen Nuytemans; Bram Meeus; David Crosiers; Nathalie Brouwers; Dirk Goossens; Sebastiaan Engelborghs; Philippe Pals; Barbara Pickut; Marleen Van den Broeck; Ellen Corsmit; Patrick Cras; Peter P De Deyn; Jurgen Del-Favero; Christine Van Broeckhoven; Jessie Theuns
Journal:  Hum Mutat       Date:  2009-07       Impact factor: 4.878

9.  EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias.

Authors:  H F Harbo; J Finsterer; J Baets; C Van Broeckhoven; S Di Donato; B Fontaine; P De Jonghe; A Lossos; T Lynch; C Mariotti; L Schöls; A Spinazzola; Z Szolnoki; S J Tabrizi; C Tallaksen; M Zeviani; J-M Burgunder; T Gasser
Journal:  Eur J Neurol       Date:  2009-05-12       Impact factor: 6.089

  9 in total
  1 in total

1.  Phenotype-driven gene target definition in clinical genome-wide sequencing data interpretation.

Authors:  Ales Maver; Luca Lovrecic; Marija Volk; Gorazd Rudolf; Karin Writzl; Ana Blatnik; Alenka Hodzic; Peterlin Borut
Journal:  Genet Med       Date:  2016-03-31       Impact factor: 8.822

  1 in total

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