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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1979 1
1988 1
1989 3
1990 9
1991 8
1992 8
1993 4
1994 4
1995 3
1996 5
1997 3
1998 7
1999 7
2000 10
2001 8
2002 7
2003 9
2004 7
2005 14
2006 11
2007 4
2008 7
2009 6
2010 5
2011 5
2012 7
2013 6
2014 9
2015 6
2016 5
2017 1
2021 1
2024 0

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180 results

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Page 1
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.
Sidransky E, Nalls MA, Aasly JO, Aharon-Peretz J, Annesi G, Barbosa ER, Bar-Shira A, Berg D, Bras J, Brice A, Chen CM, Clark LN, Condroyer C, De Marco EV, Dürr A, Eblan MJ, Fahn S, Farrer MJ, Fung HC, Gan-Or Z, Gasser T, Gershoni-Baruch R, Giladi N, Griffith A, Gurevich T, Januario C, Kropp P, Lang AE, Lee-Chen GJ, Lesage S, Marder K, Mata IF, Mirelman A, Mitsui J, Mizuta I, Nicoletti G, Oliveira C, Ottman R, Orr-Urtreger A, Pereira LV, Quattrone A, Rogaeva E, Rolfs A, Rosenbaum H, Rozenberg R, Samii A, Samaddar T, Schulte C, Sharma M, Singleton A, Spitz M, Tan EK, Tayebi N, Toda T, Troiano AR, Tsuji S, Wittstock M, Wolfsberg TG, Wu YR, Zabetian CP, Zhao Y, Ziegler SG. Sidransky E, et al. Among authors: gershoni baruch r. N Engl J Med. 2009 Oct 22;361(17):1651-61. doi: 10.1056/NEJMoa0901281. N Engl J Med. 2009. PMID: 19846850 Free PMC article.
Interstitial deletion (6)q13q15.
Gershoni-Baruch R, Mandel H, Bar El H, Bar-Nizan N, Borochowitz Z, Dar H. Gershoni-Baruch R, et al. Am J Med Genet. 1996 Apr 24;62(4):345-7. doi: 10.1002/(SICI)1096-8628(19960424)62:4<345::AID-AJMG4>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8723062 Review.
SMPD1 mutations and Parkinson disease.
Dagan E, Adir V, Schlesinger I, Borochowitz Z, Ayoub M, Mory A, Nassar M, Kurolap A, Aharon-Peretz J, Gershoni-Baruch R. Dagan E, et al. Among authors: gershoni baruch r. Parkinsonism Relat Disord. 2015 Oct;21(10):1296-7. doi: 10.1016/j.parkreldis.2015.08.019. Epub 2015 Aug 20. Parkinsonism Relat Disord. 2015. PMID: 26318962 No abstract available.
Permanent neonatal diabetes.
Bakri D, Gershoni-Baruch R, Shehadeh N. Bakri D, et al. Among authors: gershoni baruch r. Isr Med Assoc J. 2004 May;6(5):290-1. Isr Med Assoc J. 2004. PMID: 15151370 Free article. No abstract available.
Anticipation in hereditary breast cancer.
Dagan E, Gershoni-Baruch R. Dagan E, et al. Among authors: gershoni baruch r. Clin Genet. 2002 Aug;62(2):147-50. doi: 10.1034/j.1399-0004.2002.620207.x. Clin Genet. 2002. PMID: 12220452
Hereditary microphthalmia with colobomatous cyst.
Porges Y, Gershoni-Baruch R, Leibu R, Goldscher D, Zonis S, Shapira I, Miller B. Porges Y, et al. Among authors: gershoni baruch r. Am J Ophthalmol. 1992 Jul 15;114(1):30-4. doi: 10.1016/s0002-9394(14)77409-4. Am J Ophthalmol. 1992. PMID: 1621783
Camurati-Engelmann disease. Review of radioclinical features.
Vanhoenacker FM, Janssens K, Van Hul W, Gershoni-Baruch R, Brik R, De Schepper AM. Vanhoenacker FM, et al. Among authors: gershoni baruch r. Acta Radiol. 2003 Jul;44(4):430-4. doi: 10.1080/j.1600-0455.2003.00088.x. Acta Radiol. 2003. PMID: 12846694
180 results