Reish O - Search Results

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.

2

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

3

Neurodevelopmental and behavioral abnormalities associated with deletion of chromosome 9p.

Eshel G, Lahat E, Reish O, Barr J. Eshel G, et al. Among authors: reish o. J Child Neurol. 2002 Jan;17(1):50-1. doi: 10.1177/088307380201700113. J Child Neurol. 2002. PMID: 11913572

4

Founder mutation(s) in the RSPH9 gene leading to primary ciliary dyskinesia in two inbred Bedouin families.

Reish O, Slatkin M, Chapman-Shimshoni D, Elizur A, Chioza B, Castleman V, Mitchison HM. Reish O, et al. Ann Hum Genet. 2010 Mar;74(2):117-25. doi: 10.1111/j.1469-1809.2009.00559.x. Epub 2010 Jan 8. Ann Hum Genet. 2010. PMID: 20070851 Free PMC article.

5

Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) gene.

Fullston T, Finnis M, Hackett A, Hodgson B, Brueton L, Baynam G, Norman A, Reish O, Shoubridge C, Gecz J. Fullston T, et al. Among authors: reish o. Clin Genet. 2011 Dec;80(6):510-22. doi: 10.1111/j.1399-0004.2011.01685.x. Epub 2011 May 18. Clin Genet. 2011. PMID: 21496008

6

Chorioangioma and its severe infantile sequelae: case report.

Maymon R, Hermann G, Reish O, Herman A, Strauss S, Sherman D, Heyman E. Maymon R, et al. Among authors: reish o. Prenat Diagn. 2003 Dec 15;23(12):976-80. doi: 10.1002/pd.738. Prenat Diagn. 2003. PMID: 14663833

7

Prenatal diagnosis of sex chromosome abnormalities: the 8-year experience of a single medical center.

Vaknin Z, Reish O, Ben-Ami I, Heyman E, Herman A, Maymon R. Vaknin Z, et al. Among authors: reish o. Fetal Diagn Ther. 2008;23(1):76-81. doi: 10.1159/000109231. Epub 2007 Oct 9. Fetal Diagn Ther. 2008. PMID: 17934303

8

A novel de novo 27 bp duplication of the ARX gene, resulting from postzygotic mosaicism and leading to three severely affected males in two generations.

Reish O, Fullston T, Regev M, Heyman E, Gecz J. Reish O, et al. Am J Med Genet A. 2009 Aug;149A(8):1655-60. doi: 10.1002/ajmg.a.32842. Am J Med Genet A. 2009. PMID: 19606478

9

Wiedemann-Beckwith syndrome: further prenatal characterization of the condition.

Reish O, Lerer I, Amiel A, Heyman E, Herman A, Dolfin T, Abeliovich D. Reish O, et al. Am J Med Genet. 2002 Jan 22;107(3):209-13. doi: 10.1002/ajmg.10143. Am J Med Genet. 2002. PMID: 11807901 Review.

10

Prenatal diagnosis of Down syndrome: ten year experience in the Israeli population.

Shohat M, Frimer H, Shohat-Levy V, Esmailzadeh H, Appelman Z, Ben-Neriah Z, Dar H, Orr-Urtreger A, Amiel A, Gershoni R, Manor E, Barkai G, Shalev S, Gelman-Kohen Z, Reish O, Lev D, Davidov B, Goldman B. Shohat M, et al. Among authors: reish o. Am J Med Genet A. 2003 Oct 15;122A(3):215-22. doi: 10.1002/ajmg.a.20246. Am J Med Genet A. 2003. PMID: 12966521

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