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| 1 | Dysphagia in elderly nurs ing home residents with severe cognitive impairment can be atten uated by cervical spine mobilization显示文摘 | Bautmans I Demarteau J Cruts B | 2008 | J Rehabil Med2008，40，： | 1 |
| 2 | The α2-macroglobulin gene in AD:a population-based study and meta-analysis显示文摘 | Koster MN Dermaut B Cruts M | 2000 | Neurology2000，55，： | 1 |
| 3 | Amyloid betasecretase gene (BACE) is neither mutated in nor associated withearly-onset Alzheimer’s disease 显示文摘 | Cruts M Dermaut B Rademakers R | 2001 | Neurosci Lett2001，313，： | 1 |
| 4 | Locus-specific mutation databases for neurodegenerative brain diseases 显示文摘 | Cruts M Theuns J Van Broeckhoven C | 2012 | Human Mutation2012，33，9： | 1 |
| 5 | Behavioral Nonfibrillar diffuse amyloid deposition due to a gamma (42) -secretase site mutation points to an essential role for Ntruncated a beta (42) in Alheimer' s disease 显示文摘 | Kumar Singh S De Jonghe C Cruts M | 2000 | Hum Mol Gener2000，9，： | 1 |
| 6 | Estimation of the genetic contribution of presenilin-1 and -2 mutations in a poprlation-based study of presenile Alzheimer disease显示文摘 | Drijn CM Backhorens H | 1998 | Hum Mol Genet1998，7，： | 1 |
| 7 | Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21显示文摘 | Cruts M Gijselinck I van der Zee J | 2006 | Nature2006，442，： | 1 |
| 8 | The alpha2-macroglobulin gene in AD: a population-based studyand meta-analysis显示文摘 | Koster MN Dermaut B Cruts M etal | 2000 | Neurology2000，55，5： | 1 |
| 9 | Fatigue before and after mild traumatic brain injury: pre-post-injury com- parisons in relation to Apolipoprotein E 显示文摘 | Sundstrom A Nilsson LG Cruts M | 2007 | Brain Int2007，21，： | 1 |
| 10 | Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer’s disease due to a novel presenilin 1 mutation显示文摘 | B. Dermaut S. Kumar-Singh C. De Jonghe M. Cruts A. Lö fgren U. Lü bke P. Cras R. Dom P. P. De Deyn J. J. Martin | 2001 | Brain2001，，： | 1 |
| 11 | The role of tau (MAPT) in frontotemporal dementia and related tauopathies 显示文摘 | Rademakers R Cruts M Broeckhovenc | 2004 | Hum Mutat2004，24，4： | 1 |
| 12 | Loss of progranulin function in frontotempo- ral lobar degeneration 显示文摘 | Cruts M Broeckhoven C | 2008 | Trends Genet2008，24，4： | 1 |
| 13 | Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 显示文摘 | Cruts M Gijselinck I Zee J | 2006 | Nature2006，442，7105： | 1 |
| 14 | Granulin mutations associated with frontotemporal lobar degeneration and related disorders: an up- date显示文摘 | Gijselinek I Broeckhoven C Cruts M | 2008 | Hum Mutat2008，29，12： | 1 |
| 15 | 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 |
| 16 | Apolipoprotein E 4 allele in a population- based study of early-onset Alzheimer's disease显示文摘 | VanDuijn CM DeKnijff P Cruts M | 1994 | Nat Genet1994，7，1： | 1 |
| 17 | Estimation of thegenetic contribution of presenilin-1 and -2 mutations in apopulation-based study of presenile Alzheimer disease 显示文摘 | Cruts M van Duijn CM Backhovens H | 1998 | HumMol Genet1998，7，1： | 1 |
| 18 | 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 |
| 19 | Estimation of the genetic contribution of presenilin-1 and-2 mutations in a population-based study of presenile Alzheimer disease显示文摘 | Cruts M van Duijn CM Backhovens H | | 0，，： | 1 |
| 20 | 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 |
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