Blumkin L - Search Results

1

Clinical phenotypes of infantile onset CACNA1A-related disorder.

Gur-Hartman T, Berkowitz O, Yosovich K, Roubertie A, Zanni G, Macaya A, Heimer G, Dueñas BP, Sival DA, Pode-Shakked B, López-Laso E, Humbertclaude V, Riant F, Bosco L, Cayron LB, Nissenkorn A, Nicita F, Bertini E, Hassin S, Ben Zeev B, Zerem A, Libzon S, Lev D, Linder I, Lerman-Sagie T, Blumkin L. Gur-Hartman T, et al. Among authors: blumkin l. Eur J Paediatr Neurol. 2021 Jan;30:144-154. doi: 10.1016/j.ejpn.2020.10.004. Epub 2020 Oct 20. Eur J Paediatr Neurol. 2021. PMID: 33349592

2

Pediatric refractory partial status epilepticus responsive to topiramate.

Blumkin L, Lerman-Sagie T, Houri T, Gilad E, Nissenkorn A, Ginsberg M, Watemberg N. Blumkin L, et al. J Child Neurol. 2005 Mar;20(3):239-41. doi: 10.1177/08830738050200031701. J Child Neurol. 2005. PMID: 15832617

3

Nonprogressive familial leukoencephalopathy with porencephalic cyst and focal seizures.

Blumkin L, Watemberg N, Lev D, Malinger G, Luckman Y, Ben-Zeev B, Lerman-Sagie T. Blumkin L, et al. J Child Neurol. 2006 Feb;21(2):145-8. doi: 10.1177/08830738060210021701. J Child Neurol. 2006. PMID: 16566879

4

Hypomyelinating leukoencephalopathy with paroxysmal tonic upgaze and absence of psychomotor development.

Blumkin L, Lev D, Watemberg N, Lerman-Sagie T. Blumkin L, et al. Mov Disord. 2007 Jan 15;22(2):226-30. doi: 10.1002/mds.21277. Mov Disord. 2007. PMID: 17149740

5

Clinical correlates of occipital intermittent rhythmic delta activity (OIRDA) in children.

Watemberg N, Linder I, Dabby R, Blumkin L, Lerman-Sagie T. Watemberg N, et al. Among authors: blumkin l. Epilepsia. 2007 Feb;48(2):330-4. doi: 10.1111/j.1528-1167.2006.00937.x. Epilepsia. 2007. PMID: 17295627 Free article.

6

Infantile onset progressive cerebellar atrophy and anterior horn cell degeneration--a late onset variant of PCH-1?

Lev D, Michelson-Kerman M, Vinkler C, Blumkin L, Shalev SA, Lerman-Sagie T. Lev D, et al. Among authors: blumkin l. Eur J Paediatr Neurol. 2008 Mar;12(2):97-101. doi: 10.1016/j.ejpn.2007.06.005. Epub 2007 Jul 30. Eur J Paediatr Neurol. 2008. PMID: 17681808

7

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. 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

8

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. J Child Neurol. 2010 Jul;25(7):892-7. doi: 10.1177/0883073809351316. Epub 2010 Jan 21. J Child Neurol. 2010. PMID: 20097664

9

Neurologic involvement in a child with systemic capillary leak syndrome.

Sion-Sarid R, Lerman-Sagie T, Blumkin L, Ben-Ami D, Cohen I, Houri S. Sion-Sarid R, et al. Among authors: blumkin l. Pediatrics. 2010 Mar;125(3):e687-92. doi: 10.1542/peds.2009-1691. Epub 2010 Feb 1. Pediatrics. 2010. PMID: 20123768

10

Hepatic coma culminating in severe brain damage in a child with a SCN1A mutation.

Nishri D, Blumkin L, Lev D, Leshinsky-Silver E, Abu-Rashid M, Birch R, Zuberi SM, Lerman-Sagie T. Nishri D, et al. Among authors: blumkin l. Eur J Paediatr Neurol. 2010 Sep;14(5):456-9. doi: 10.1016/j.ejpn.2010.03.002. Epub 2010 Apr 13. Eur J Paediatr Neurol. 2010. PMID: 20392657

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