Lev D - Search Results

1

The molecular and phenotypic spectrum of IQSEC2-related epilepsy.

Zerem A, Haginoya K, Lev D, Blumkin L, Kivity S, Linder I, Shoubridge C, Palmer EE, Field M, Boyle J, Chitayat D, Gaillard WD, Kossoff EH, Willems M, Geneviève D, Tran-Mau-Them F, Epstein O, Heyman E, Dugan S, Masurel-Paulet A, Piton A, Kleefstra T, Pfundt R, Sato R, Tzschach A, Matsumoto N, Saitsu H, Leshinsky-Silver E, Lerman-Sagie T. Zerem A, et al. Among authors: lev d. Epilepsia. 2016 Nov;57(11):1858-1869. doi: 10.1111/epi.13560. Epub 2016 Sep 26. Epilepsia. 2016. PMID: 27665735 Free article.

2

Multiple presentation of mitochondrial disorders.

Nissenkorn A, Zeharia A, Lev D, Fatal-Valevski A, Barash V, Gutman A, Harel S, Lerman-Sagie T. Nissenkorn A, et al. Among authors: lev d. Arch Dis Child. 1999 Sep;81(3):209-14. doi: 10.1136/adc.81.3.209. Arch Dis Child. 1999. PMID: 10451392 Free PMC article.

3

Neurologic presentations of mitochondrial disorders.

Nissenkorn A, Zeharia A, Lev D, Watemberg N, Fattal-Valevski A, Barash V, Gutman A, Harel S, Lerman-Sagie T. Nissenkorn A, et al. Among authors: lev d. J Child Neurol. 2000 Jan;15(1):44-8. doi: 10.1177/088307380001500110. J Child Neurol. 2000. PMID: 10641610

4

Familial mitochondrial intestinal pseudo-obstruction and neurogenic bladder.

Haftel LT, Lev D, Barash V, Gutman A, Bujanover Y, Lerman-Sagie T. Haftel LT, et al. Among authors: lev d. J Child Neurol. 2000 Jun;15(6):386-9. doi: 10.1177/088307380001500606. J Child Neurol. 2000. PMID: 10868781

5

[Mitochondrial diseases: molecular genetics and clinical applications].

Leshinsky-Silver E, Lev D, Lerman-Sagie T. Leshinsky-Silver E, et al. Among authors: lev d. Harefuah. 2000 Feb 1;138(3):220-9. Harefuah. 2000. PMID: 10883098 Review. Hebrew. No abstract available.

6

Dramatic improvement in mitochondrial cardiomyopathy following treatment with idebenone.

Lerman-Sagie T, Rustin P, Lev D, Yanoov M, Leshinsky-Silver E, Sagie A, Ben-Gal T, Munnich A. Lerman-Sagie T, et al. Among authors: lev d. J Inherit Metab Dis. 2001 Feb;24(1):28-34. doi: 10.1023/a:1005642302316. J Inherit Metab Dis. 2001. PMID: 11286379

7

Febrile convulsions, ataxia, developmental delay, and obesity: a new syndrome?

Lev D, Watemberg N, Aviram A, Fishoff J, Antman E, Lerman-Sagie T. Lev D, et al. J Child Neurol. 2001 Mar;16(3):174-6. doi: 10.1177/088307380101600304. J Child Neurol. 2001. PMID: 11305685

8

Behavioral phenotypes of genetic syndromes: a reference guide for psychiatrists.

Moldavsky M, Lev D, Lerman-Sagie T. Moldavsky M, et al. Among authors: lev d. J Am Acad Child Adolesc Psychiatry. 2001 Jul;40(7):749-61. doi: 10.1097/00004583-200107000-00009. J Am Acad Child Adolesc Psychiatry. 2001. PMID: 11437013 Review.

9

The fetal cerebellar vermis: normal development as shown by transvaginal ultrasound.

Malinger G, Ginath S, Lerman-Sagie T, Watemberg N, Lev D, Glezerman M. Malinger G, et al. Among authors: lev d. Prenat Diagn. 2001 Aug;21(8):687-92. doi: 10.1002/pd.137. Prenat Diagn. 2001. PMID: 11536272

10

White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation.

Lev D, Yanoov-Sharav M, Watemberg N, Leshinsky-Silver E, Lerman-Sagie T. Lev D, et al. Eur J Paediatr Neurol. 2002;6(2):121-3. doi: 10.1053/ejpn.2001.0558. Eur J Paediatr Neurol. 2002. PMID: 11995959

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