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636 results

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Page 1
Substantia nigra hyperechogenicity with LRRK2 G2019S mutations.
Brüggemann N, Hagenah J, Stanley K, Klein C, Wang C, Raymond D, Ozelius L, Bressman S, Saunders-Pullman R. Brüggemann N, et al. Among authors: stanley k. Mov Disord. 2011 Apr;26(5):885-8. doi: 10.1002/mds.23644. Epub 2011 Feb 10. Mov Disord. 2011. PMID: 21312285 Free PMC article.
Olfactory dysfunction in LRRK2 G2019S mutation carriers.
Saunders-Pullman R, Stanley K, Wang C, San Luciano M, Shanker V, Hunt A, Severt L, Raymond D, Ozelius LJ, Lipton RB, Bressman SB. Saunders-Pullman R, et al. Among authors: stanley k. Neurology. 2011 Jul 26;77(4):319-24. doi: 10.1212/WNL.0b013e318227041c. Epub 2011 Jul 13. Neurology. 2011. PMID: 21753159 Free PMC article.
LRRK2 G2019S mutations may be increased in Puerto Ricans.
Saunders-Pullman R, Cabassa J, San Luciano M, Stanley K, Raymond D, Ozelius LJ, Bressman SB. Saunders-Pullman R, et al. Among authors: stanley k. Mov Disord. 2011 Aug 1;26(9):1772-3. doi: 10.1002/mds.23632. Epub 2011 Mar 29. Mov Disord. 2011. PMID: 21449009 Free PMC article. No abstract available.
Gender differences in the risk of familial parkinsonism: beyond LRRK2?
Saunders-Pullman R, Stanley K, San Luciano M, Barrett MJ, Shanker V, Raymond D, Ozelius LJ, Bressman SB. Saunders-Pullman R, et al. Among authors: stanley k. Neurosci Lett. 2011 Jun 1;496(2):125-8. doi: 10.1016/j.neulet.2011.03.098. Epub 2011 Apr 12. Neurosci Lett. 2011. PMID: 21511009 Free PMC article.
Transcranial sonography and functional imaging in glucocerebrosidase mutation Parkinson disease.
Barrett MJ, Hagenah J, Dhawan V, Peng S, Stanley K, Raymond D, Deik A, Gross SJ, Schreiber-Agus N, Mirelman A, Marder K, Ozelius LJ, Eidelberg D, Bressman SB, Saunders-Pullman R; LRRK2 Ashkenazi Jewish Consortium. Barrett MJ, et al. Among authors: stanley k. Parkinsonism Relat Disord. 2013 Feb;19(2):186-91. doi: 10.1016/j.parkreldis.2012.09.007. Epub 2012 Oct 10. Parkinsonism Relat Disord. 2013. PMID: 23062841 Free PMC article.
Validity of spiral analysis in early Parkinson's disease.
Saunders-Pullman R, Derby C, Stanley K, Floyd A, Bressman S, Lipton RB, Deligtisch A, Severt L, Yu Q, Kurtis M, Pullman SL. Saunders-Pullman R, et al. Among authors: stanley k. Mov Disord. 2008 Mar 15;23(4):531-7. doi: 10.1002/mds.21874. Mov Disord. 2008. PMID: 18074362
Substantia nigra hyperechogenicity in DYT6 dystonia: a pilot study.
Saunders-Pullman R, Stanley K, Brüggemann N, Raymond D, San Luciano M, Wang C, Klein C, Lubarr N, Ozelius L, Bressman SB, Hagenah J. Saunders-Pullman R, et al. Among authors: stanley k. Parkinsonism Relat Disord. 2010 Jul;16(6):420-2. doi: 10.1016/j.parkreldis.2010.03.003. Epub 2010 Apr 22. Parkinsonism Relat Disord. 2010. PMID: 20417146 Free PMC article. No abstract available.
Diagnosis and referral delay in women with Parkinson's disease.
Saunders-Pullman R, Wang C, Stanley K, Bressman SB. Saunders-Pullman R, et al. Among authors: stanley k. Gend Med. 2011 Jun;8(3):209-17. doi: 10.1016/j.genm.2011.05.002. Gend Med. 2011. PMID: 21664587 Free PMC article.
636 results