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Page 1
Comprehensive screening of a North American Parkinson's disease cohort for LRRK2 mutation.
Johnson J, Paisán-Ruíz C, Lopez G, Crews C, Britton A, Malkani R, Evans EW, McInerney-Leo A, Jain S, Nussbaum RL, Foote KD, Mandel RJ, Crawley A, Reimsnider S, Fernandez HH, Okun MS, Gwinn-Hardy K, Singleton AB. Johnson J, et al. Neurodegener Dis. 2007;4(5):386-91. doi: 10.1159/000105160. Epub 2007 Jul 6. Neurodegener Dis. 2007. PMID: 17622782
Turner syndrome: four challenges across the lifespan.
Sutton EJ, McInerney-Leo A, Bondy CA, Gollust SE, King D, Biesecker B. Sutton EJ, et al. Am J Med Genet A. 2005 Dec 1;139A(2):57-66. doi: 10.1002/ajmg.a.30911. Am J Med Genet A. 2005. PMID: 16252273 Free PMC article.
Mutations That Alter the Carboxy-Terminal-Propeptide Cleavage Site of the Chains of Type I Procollagen Are Associated With a Unique Osteogenesis Imperfecta Phenotype.
Cundy T, Dray M, Delahunt J, Hald JD, Langdahl B, Li C, Szybowska M, Mohammed S, Duncan EL, McInerney-Leo AM, Wheeler PG, Roschger P, Klaushofer K, Rai J, Weis M, Eyre D, Schwarze U, Byers PH. Cundy T, et al. J Bone Miner Res. 2018 Jul;33(7):1260-1271. doi: 10.1002/jbmr.3424. Epub 2018 Apr 18. J Bone Miner Res. 2018. PMID: 29669177 Free PMC article.
Genetic testing in Parkinson's disease.
McInerney-Leo A. McInerney-Leo A. Mov Disord. 2005 Jul;20(7):908-9. doi: 10.1002/mds.20509. Mov Disord. 2005. PMID: 15884041 No abstract available.
Genetic testing in Parkinson's disease.
McInerney-Leo A, Hadley DW, Gwinn-Hardy K, Hardy J. McInerney-Leo A, et al. Mov Disord. 2005 Jan;20(1):1-10. doi: 10.1002/mds.20316. Mov Disord. 2005. PMID: 15503301 Review.
106 results