Lerman-Sagie T - Search Results

1

Deficiency of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathy.

Ruzzo EK, Capo-Chichi JM, Ben-Zeev B, Chitayat D, Mao H, Pappas AL, Hitomi Y, Lu YF, Yao X, Hamdan FF, Pelak K, Reznik-Wolf H, Bar-Joseph I, Oz-Levi D, Lev D, Lerman-Sagie T, Leshinsky-Silver E, Anikster Y, Ben-Asher E, Olender T, Colleaux L, Décarie JC, Blaser S, Banwell B, Joshi RB, He XP, Patry L, Silver RJ, Dobrzeniecka S, Islam MS, Hasnat A, Samuels ME, Aryal DK, Rodriguiz RM, Jiang YH, Wetsel WC, McNamara JO, Rouleau GA, Silver DL, Lancet D, Pras E, Mitchell GA, Michaud JL, Goldstein DB. Ruzzo EK, et al. Neuron. 2013 Oct 16;80(2):429-41. doi: 10.1016/j.neuron.2013.08.013. Neuron. 2013. PMID: 24139043 Free PMC article.

2

[Mitochondrial diseases: molecular genetics and clinical applications].

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

3

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

Moldavsky M, Lev D, Lerman-Sagie T. Moldavsky M, et al. 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.

4

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

5

A new autosomal recessive syndrome with Zellweger-like manifestations.

Ahn JK, Lev D, Leshinsky-Silver E, Ginzberg M, Lerman-Sagie T. Ahn JK, et al. Am J Med Genet A. 2003 Jun 15;119A(3):352-5. doi: 10.1002/ajmg.a.20124. Am J Med Genet A. 2003. PMID: 12784304

6

The first nonsense mutation in alsin results in a homogeneous phenotype of infantile-onset ascending spastic paralysis with bulbar involvement in two siblings.

Devon RS, Helm JR, Rouleau GA, Leitner Y, Lerman-Sagie T, Lev D, Hayden MR. Devon RS, et al. Clin Genet. 2003 Sep;64(3):210-5. doi: 10.1034/j.1399-0004.2003.00138.x. Clin Genet. 2003. PMID: 12919135

7

Progressive cerebellocerebral atrophy: a new syndrome with microcephaly, mental retardation, and spastic quadriplegia.

Ben-Zeev B, Hoffman C, Lev D, Watemberg N, Malinger G, Brand N, Lerman-Sagie T. Ben-Zeev B, et al. J Med Genet. 2003 Aug;40(8):e96. doi: 10.1136/jmg.40.8.e96. J Med Genet. 2003. PMID: 12920088 Free PMC article. No abstract available.

8

Familial optic atrophy with white matter changes.

Vinkler C, Lev D, Kalish H, Watemberg N, Yanoov-Sharav M, Leshinsky-Silver E, Lerman-Sagie T. Vinkler C, et al. Am J Med Genet A. 2003 Sep 1;121A(3):263-5. doi: 10.1002/ajmg.a.20238. Am J Med Genet A. 2003. PMID: 12923868

9

Assessment of fetal intracranial pathologies first demonstrated late in pregnancy: cell proliferation disorders.

Malinger G, Lev D, Lerman-Sagie T. Malinger G, et al. Reprod Biol Endocrinol. 2003 Nov 14;1:110. doi: 10.1186/1477-7827-1-110. Reprod Biol Endocrinol. 2003. PMID: 14617366 Free PMC article. Review.

10

Should autistic children be evaluated for mitochondrial disorders?

Lerman-Sagie T, Leshinsky-Silver E, Watemberg N, Lev D. Lerman-Sagie T, et al. J Child Neurol. 2004 May;19(5):379-81. doi: 10.1177/088307380401900510. J Child Neurol. 2004. PMID: 15224710 Review.

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