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

Year Number of Results
1985 2
1987 5
1988 2
1989 3
1990 2
1991 2
1994 1
1995 6
1996 3
1997 4
1998 5
1999 12
2000 10
2001 9
2002 10
2003 13
2004 13
2005 9
2006 9
2007 15
2008 9
2009 10
2010 17
2011 18
2012 15
2013 10
2014 14
2015 14
2016 17
2017 7
2018 20
2019 12
2020 11
2021 6
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285 results
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Page 1
Fetal cerebellar disorders.
Lerman-Sagie T, Prayer D, Stöcklein S, Malinger G. Lerman-Sagie T, et al. Handb Clin Neurol. 2018;155:3-23. doi: 10.1016/B978-0-444-64189-2.00001-9. Handb Clin Neurol. 2018. PMID: 29891067 Review.
Diagnostic approach to fetal microcephaly.
Leibovitz Z, Lerman-Sagie T. Leibovitz Z, et al. Among authors: lerman sagie t. Eur J Paediatr Neurol. 2018 Nov;22(6):935-943. doi: 10.1016/j.ejpn.2018.06.002. Epub 2018 Jun 30. Eur J Paediatr Neurol. 2018. PMID: 29970280 Review.
A clinical diagnostic algorithm for early onset cerebellar ataxia.
Brandsma R, Verschuuren-Bemelmans CC, Amrom D, Barisic N, Baxter P, Bertini E, Blumkin L, Brankovic-Sreckovic V, Brouwer OF, Bürk K, Catsman-Berrevoets CE, Craiu D, de Coo IFM, Gburek J, Kennedy C, de Koning TJ, Kremer HPH, Kumar R, Macaya A, Micalizzi A, Mirabelli-Badenier M, Nemeth A, Nuovo S, Poll-The B, Lerman-Sagie T, Steinlin M, Synofzik M, Tijssen MAJ, Vasco G, Willemsen MAAP, Zanni G, Valente EM, Boltshauser E, Sival DA. Brandsma R, et al. Among authors: lerman sagie t. Eur J Paediatr Neurol. 2019 Sep;23(5):692-706. doi: 10.1016/j.ejpn.2019.08.004. Epub 2019 Aug 10. Eur J Paediatr Neurol. 2019. PMID: 31481303 Review.
Medical Cannabis for Pediatric Moderate to Severe Complex Motor Disorders.
Libzon S, Schleider LB, Saban N, Levit L, Tamari Y, Linder I, Lerman-Sagie T, Blumkin L. Libzon S, et al. Among authors: lerman sagie t. J Child Neurol. 2018 Aug;33(9):565-571. doi: 10.1177/0883073818773028. Epub 2018 May 16. J Child Neurol. 2018. PMID: 29766748 Clinical Trial.
Systematic review and meta-analysis of isolated posterior fossa malformations on prenatal ultrasound imaging (part 1): nomenclature, diagnostic accuracy and associated anomalies.
D'Antonio F, Khalil A, Garel C, Pilu G, Rizzo G, Lerman-Sagie T, Bhide A, Thilaganathan B, Manzoli L, Papageorghiou AT. D'Antonio F, et al. Among authors: lerman sagie t. Ultrasound Obstet Gynecol. 2016 Jun;47(6):690-7. doi: 10.1002/uog.14900. Epub 2016 May 10. Ultrasound Obstet Gynecol. 2016. PMID: 25970099 Free article. Review.
Lacosamide for SCN2A-related intractable neonatal and infantile seizures.
Flor-Hirsch H, Heyman E, Livneh A, Reish O, Watemberg N, Litmanovits I, Ben Sason Lilli A, Lev D, Lerman Sagie T, Bassan H. Flor-Hirsch H, et al. Among authors: lerman sagie t. Epileptic Disord. 2018 Oct 1;20(5):440-446. doi: 10.1684/epd.2018.1001. Epileptic Disord. 2018. PMID: 30361185 Free article.
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes.
Rivière JB, Mirzaa GM, O'Roak BJ, Beddaoui M, Alcantara D, Conway RL, St-Onge J, Schwartzentruber JA, Gripp KW, Nikkel SM, Worthylake T, Sullivan CT, Ward TR, Butler HE, Kramer NA, Albrecht B, Armour CM, Armstrong L, Caluseriu O, Cytrynbaum C, Drolet BA, Innes AM, Lauzon JL, Lin AE, Mancini GM, Meschino WS, Reggin JD, Saggar AK, Lerman-Sagie T, Uyanik G, Weksberg R, Zirn B, Beaulieu CL; Finding of Rare Disease Genes (FORGE) Canada Consortium, Majewski J, Bulman DE, O'Driscoll M, Shendure J, Graham JM Jr, Boycott KM, Dobyns WB. Rivière JB, et al. Among authors: lerman sagie t. Nat Genet. 2012 Jun 24;44(8):934-40. doi: 10.1038/ng.2331. Nat Genet. 2012. PMID: 22729224 Free PMC article.
285 results
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