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| 1 | Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family显示文摘 | Brouwers N Nuytemans K van der Zee J | 2007 | Arch Neurol2007，64，10： | 1 |
| 2 | Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease显示文摘 | Bogaerts V Nuytemans K Reumers J | 2008 | Hum Mutat2008，29，6： | 1 |
| 3 | Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update显示文摘 | Nuytemans K Theuns J Cruts M | 2010 | Hum Mutat2010，31，7： | 1 |
| 4 | Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARKT, and LRRK2 genes: a mutation update显示文摘 | Nuytemans K Theuns J Cruts M | 2010 | HumMutat2010，31，7： | 1 |
| 5 | GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population 显示文摘 | Meeus B Nuytemans K Crosiers D | 2011 | Neurobiol Aging2011，32，2： | 1 |
| 6 | C9ORt72 intermediate repeat copies are a significant risk factor for Parkinson disease显示文摘 | Nuytemans K Bademci G Kohli MM | 2013 | Ann Hum Genet2013，77，5： | 1 |
| 7 | Genetic etiology ofParkinson disease associated with mutations in the SNCA,PARK2, PINK1, PARK7, and LRRK2 genes: a mutation up-date显示文摘 | Nuytemans K Theuns J Cruts M | 2010 | Hum Mutat2010，31，7： | 1 |
| 8 | A simple quantitative method analysing amikacin, gentamicin, and vancomycin levels in human newborn plasma using ion-pair liquid chromatography/tandem mass spectrometry and its applicability to a clinical study显示文摘 | Yuma Bijleveld Timo de Haan Jan Toersche Sona Jorjani Johanna van der Lee Floris Groenendaal Peter Dijk Arno van Heijst Antonio W.D. Gavilanes Rogier de Jonge Koen P. Dijkman Henrica van Straaten Monique Rijken Inge Zonnenberg Filip Cools Debbie Nuytemans | 2014 | Journal of Chromatography B2014，，： | 1 |
| 9 | Genetic Etiology of Parkinson Disease Associated with Mutations in the SNCA,PARK2,PINK1,PARK7,and LRRK2 Genes:A Mutation Update显示文摘 | Nuytemans K Theuns J Cruts M | | 0，，： | 1 |
| 10 | Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease 显示文摘 | Bogaerts V Nuytemans K Reumers J | 2008 | Hum Mutat2008，29，6： | 1 |
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