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Results by year

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

Year Number of Results
1990 1
1993 3
1994 1
1995 5
1996 2
1997 1
1998 1
1999 1
2000 2
2001 3
2002 7
2003 7
2004 2
2005 5
2006 3
2007 2
2008 3
2009 11
2010 6
2011 4
2012 1
2013 1
2014 3
2015 1
2016 2
2017 2
2018 3
2019 1
2020 2
2021 1
2023 1

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81 results

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Page 1
SCN3A-Related Neurodevelopmental Disorder: A Spectrum of Epilepsy and Brain Malformation.
Zaman T, Helbig KL, Clatot J, Thompson CH, Kang SK, Stouffs K, Jansen AE, Verstraete L, Jacquinet A, Parrini E, Guerrini R, Fujiwara Y, Miyatake S, Ben-Zeev B, Bassan H, Reish O, Marom D, Hauser N, Vu TA, Ackermann S, Spencer CE, Lippa N, Srinivasan S, Charzewska A, Hoffman-Zacharska D, Fitzpatrick D, Harrison V, Vasudevan P, Joss S, Pilz DT, Fawcett KA, Helbig I, Matsumoto N, Kearney JA, Fry AE, Goldberg EM. Zaman T, et al. Among authors: reish o. Ann Neurol. 2020 Aug;88(2):348-362. doi: 10.1002/ana.25809. Epub 2020 Jul 9. Ann Neurol. 2020. PMID: 32515017 Free PMC article.
Uterine cancer in Jewish Israeli BRCA1/2 mutation carriers.
Laitman Y, Michaelson-Cohen R, Levi E, Chen-Shtoyerman R, Reish O, Josefsberg Ben-Yehoshua S, Bernstein-Molho R, Keinan-Boker L, Rosengarten O, Silverman BG, Perri T, Korach J, Mor P, Ephrat Ben-Baruch N, Levy Lahad E, Friedman E; Israeli Consortium of Hereditary Breast Cancer. Laitman Y, et al. Among authors: reish o. Cancer. 2019 Mar 1;125(5):698-703. doi: 10.1002/cncr.31842. Epub 2018 Nov 29. Cancer. 2019. PMID: 30489631 Free article.
A Homozygous Nme7 Mutation Is Associated with Situs Inversus Totalis.
Reish O, Aspit L, Zouella A, Roth Y, Polak-Charcon S, Baboushkin T, Benyamini L, Scheetz TE, Mussaffi H, Sheffield VC, Parvari R. Reish O, et al. Hum Mutat. 2016 Aug;37(8):727-31. doi: 10.1002/humu.22998. Epub 2016 May 9. Hum Mutat. 2016. PMID: 27060491 Free PMC article.
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: reish o. Epileptic Disord. 2018 Oct 1;20(5):440-446. doi: 10.1684/epd.2018.1001. Epileptic Disord. 2018. PMID: 30361185
Congenital hypothyroidism with Prader-Willi syndrome.
Sher C, Bistritzer T, Reisler G, Reish O. Sher C, et al. Among authors: reish o. J Pediatr Endocrinol Metab. 2002 Jan;15(1):105-7. doi: 10.1515/jpem.2002.15.1.105. J Pediatr Endocrinol Metab. 2002. PMID: 11822575
Congenital myopathy is caused by mutation of HACD1.
Muhammad E, Reish O, Ohno Y, Scheetz T, Deluca A, Searby C, Regev M, Benyamini L, Fellig Y, Kihara A, Sheffield VC, Parvari R. Muhammad E, et al. Among authors: reish o. Hum Mol Genet. 2013 Dec 20;22(25):5229-36. doi: 10.1093/hmg/ddt380. Epub 2013 Aug 9. Hum Mol Genet. 2013. PMID: 23933735 Free PMC article.
81 results