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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 4
2009 5
2010 4
2011 5
2012 6
2013 4
2014 6
2015 5
2016 5
2017 1
2021 1
2022 0
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170 results
Results by year
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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.
Tel Hashomer camptodactyly syndrome in identical twin infants.
Smolkin T, Blazer S, Gershoni-Baruch R, Makhoul IR. Smolkin T, et al. Among authors: gershoni baruch r. Clin Dysmorphol. 2011 Oct;20(4):214-216. doi: 10.1097/MCD.0b013e32834a044f. Clin Dysmorphol. 2011. PMID: 21814136 Review. No abstract available.
Accessory male pseudogenitalia?
Makhoul IR, Shoshany G, Gershoni-Baruch R, Hardak B, Gaitini D. Makhoul IR, et al. Among authors: gershoni baruch r. J Pediatr. 2006 Aug;149(2):278. doi: 10.1016/j.jpeds.2006.02.040. J Pediatr. 2006. PMID: 16887453 No abstract available.
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.
170 results