Kivity S - Search Results

1

Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutation.

Blumkin L, Suls A, Deconinck T, De Jonghe P, Linder I, Kivity S, Dabby R, Leshinsky-Silver E, Lev D, Lerman-Sagie T. Blumkin L, et al. Among authors: kivity s. Eur J Paediatr Neurol. 2012 Jul;16(4):356-60. doi: 10.1016/j.ejpn.2011.11.004. Epub 2011 Dec 14. Eur J Paediatr Neurol. 2012. PMID: 22169383

2

Familial leukoencephalopathy with slowly progressive dystonia and ataxia.

Blumkin L, Mandel H, Anca-Herschkovitsch M, Kivity S, Lev D, Lerman-Sagie T. Blumkin L, et al. Among authors: kivity s. Eur J Paediatr Neurol. 2009 Nov;13(6):530-3. doi: 10.1016/j.ejpn.2008.11.004. Epub 2008 Dec 13. Eur J Paediatr Neurol. 2009. PMID: 19071044

3

Congenital ataxia, mental retardation, and dyskinesia associated with a novel CACNA1A mutation.

Blumkin L, Michelson M, Leshinsky-Silver E, Kivity S, Lev D, Lerman-Sagie T. Blumkin L, et al. Among authors: kivity s. J Child Neurol. 2010 Jul;25(7):892-7. doi: 10.1177/0883073809351316. Epub 2010 Jan 21. J Child Neurol. 2010. PMID: 20097664

4

A compound heterozygous missense mutation and a large deletion in the KCTD7 gene presenting as an opsoclonus-myoclonus ataxia-like syndrome.

Blumkin L, Kivity S, Lev D, Cohen S, Shomrat R, Lerman-Sagie T, Leshinsky-Silver E. Blumkin L, et al. Among authors: kivity s. J Neurol. 2012 Dec;259(12):2590-8. doi: 10.1007/s00415-012-6545-z. Epub 2012 May 26. J Neurol. 2012. PMID: 22638565

5

Paternal germline mosaicism of a SCN2A mutation results in Ohtahara syndrome in half siblings.

Zerem A, Lev D, Blumkin L, Goldberg-Stern H, Michaeli-Yossef Y, Halevy A, Kivity S, Nakamura K, Matsumoto N, Leshinsky-Silver E, Saitsu H, Lerman-Sagie T. Zerem A, et al. Among authors: kivity s. Eur J Paediatr Neurol. 2014 Sep;18(5):567-71. doi: 10.1016/j.ejpn.2014.04.008. Epub 2014 Apr 18. Eur J Paediatr Neurol. 2014. PMID: 24814476

6

Paroxysmal tonic upward gaze as a presentation of de-novo mutations in CACNA1A.

Blumkin L, Leshinsky-Silver E, Michelson M, Zerem A, Kivity S, Lev D, Lerman-Sagie T. Blumkin L, et al. Among authors: kivity s. Eur J Paediatr Neurol. 2015 May;19(3):292-7. doi: 10.1016/j.ejpn.2014.12.018. Epub 2015 Jan 8. Eur J Paediatr Neurol. 2015. PMID: 25596066

7

Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome.

Grinton BE, Heron SE, Pelekanos JT, Zuberi SM, Kivity S, Afawi Z, Williams TC, Casalaz DM, Yendle S, Linder I, Lev D, Lerman-Sagie T, Malone S, Bassan H, Goldberg-Stern H, Stanley T, Hayman M, Calvert S, Korczyn AD, Shevell M, Scheffer IE, Mulley JC, Berkovic SF. Grinton BE, et al. Among authors: kivity s. Epilepsia. 2015 Jul;56(7):1071-80. doi: 10.1111/epi.13020. Epub 2015 May 15. Epilepsia. 2015. PMID: 25982755 Free article.

8

Atypical presentation of Costeff syndrome-severe psychomotor involvement and electrical status epilepticus during slow wave sleep.

Carmi N, Lev D, Leshinsky-Silver E, Anikster Y, Blumkin L, Kivity S, Lerman-Sagie T, Zerem A. Carmi N, et al. Among authors: kivity s. Eur J Paediatr Neurol. 2015 Nov;19(6):733-6. doi: 10.1016/j.ejpn.2015.06.006. Epub 2015 Jul 9. Eur J Paediatr Neurol. 2015. PMID: 26190011

9

RARS2 mutations cause early onset epileptic encephalopathy without ponto-cerebellar hypoplasia.

Nishri D, Goldberg-Stern H, Noyman I, Blumkin L, Kivity S, Saitsu H, Nakashima M, Matsumoto N, Leshinsky-Silver E, Lerman-Sagie T, Lev D. Nishri D, et al. Among authors: kivity s. Eur J Paediatr Neurol. 2016 May;20(3):412-7. doi: 10.1016/j.ejpn.2016.02.012. Epub 2016 Mar 2. Eur J Paediatr Neurol. 2016. PMID: 26970947

10

Resolution of epileptic encephalopathy following treatment with transdermal nicotine.

Zerem A, Nishri D, Yosef Y, Blumkin L, Lev D, Leshinsky-Silver E, Kivity S, Lerman-Sagie T. Zerem A, et al. Among authors: kivity s. Epilepsia. 2013 Jan;54(1):e13-5. doi: 10.1111/j.1528-1167.2012.03715.x. Epub 2012 Oct 12. Epilepsia. 2013. PMID: 23061632 Free article.

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