Tenenbaum-Rakover Y - Search Results

1

Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity.

Tornovsky S, Crane A, Cosgrove KE, Hussain K, Lavie J, Heyman M, Nesher Y, Kuchinski N, Ben-Shushan E, Shatz O, Nahari E, Potikha T, Zangen D, Tenenbaum-Rakover Y, de Vries L, Argente J, Gracia R, Landau H, Eliakim A, Lindley K, Dunne MJ, Aguilar-Bryan L, Glaser B. Tornovsky S, et al. J Clin Endocrinol Metab. 2004 Dec;89(12):6224-34. doi: 10.1210/jc.2004-1233. J Clin Endocrinol Metab. 2004. PMID: 15579781

2

Novel mutations in epithelial sodium channel (ENaC) subunit genes and phenotypic expression of multisystem pseudohypoaldosteronism.

Edelheit O, Hanukoglu I, Gizewska M, Kandemir N, Tenenbaum-Rakover Y, Yurdakök M, Zajaczek S, Hanukoglu A. Edelheit O, et al. Clin Endocrinol (Oxf). 2005 May;62(5):547-53. doi: 10.1111/j.1365-2265.2005.02255.x. Clin Endocrinol (Oxf). 2005. PMID: 15853823 Review.

3

Increase in the incidence of type 1 diabetes in Israeli children following the Second Lebanon War.

Zung A, Blumenfeld O, Shehadeh N, Dally Gottfried O, Tenenbaum Rakover Y, Hershkovitz E, Gillis D, Zangen D, Pinhas-Hamiel O, Hanukoglu A, Rachmiel M, Shalitin S; Israel IDDM Registry Study Group. Zung A, et al. Pediatr Diabetes. 2012 Jun;13(4):326-33. doi: 10.1111/j.1399-5448.2011.00838.x. Epub 2011 Dec 13. Pediatr Diabetes. 2012. PMID: 22151880

4

Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failure.

Tenenbaum-Rakover Y, Weinberg-Shukron A, Renbaum P, Lobel O, Eideh H, Gulsuner S, Dahary D, Abu-Rayyan A, Kanaan M, Levy-Lahad E, Bercovich D, Zangen D. Tenenbaum-Rakover Y, et al. J Med Genet. 2015 Jun;52(6):391-9. doi: 10.1136/jmedgenet-2014-102921. Epub 2015 Apr 14. J Med Genet. 2015. PMID: 25873734

5

Prevalence of early and late prematurity is similar among pediatric type 1 diabetes patients and the general population.

Adar A, Shalitin S, Eyal O, Loewenthal N, Pinhas-Hamiel O, Levy M, Dally-Gottfried O, Landau Z, Zung A, Levy-Khademi F, Zangen D, Tenenbaum-Rakover Y, Rachmiel M. Adar A, et al. Diabetes Metab Res Rev. 2018 Jul;34(5):e2996. doi: 10.1002/dmrr.2996. Epub 2018 Mar 24. Diabetes Metab Res Rev. 2018. PMID: 29471580

6

Combined Gestational Age- and Birth Weight-Adjusted Cutoffs for Newborn Screening of Congenital Adrenal Hyperplasia.

Pode-Shakked N, Blau A, Pode-Shakked B, Tiosano D, Weintrob N, Eyal O, Zung A, Levy-Khademi F, Tenenbaum-Rakover Y, Zangen D, Gillis D, Pinhas-Hamiel O, Loewenthal N, de Vries L, Landau Z, Rachmiel M, Abu-Libdeh A, Eliakim A, Strich D, Koren I, German A, Sack J, Almashanu S. Pode-Shakked N, et al. J Clin Endocrinol Metab. 2019 Aug 1;104(8):3172-3180. doi: 10.1210/jc.2018-02468. J Clin Endocrinol Metab. 2019. PMID: 30865229

7

Primary Ovarian Insufficiency Nationwide Incidence Rate and Etiology Among Israeli Adolescents.

Gruber N, Kugler S, de Vries L, Brener A, Zung A, Eyal O, Rachmiel M, Koren I, Tenenbaum-Rakover Y, Hershkovitz E, Landau Z, Oren M, Eliakim A, Zangen D, German A, Majdoub H, Mazor-Aronovitch K, Modan-Moses D, Yeshayahu Y, Naugolni L, Levy-Shraga Y, Ben-Ami M, Brill G, Zuckerman-Levin N, Levy-Khademi F, Avnon-Ziv C, Tiosano D, Harel S, Kedem E, Segev-Becker A, Shoenfeld Y, Pinhas-Hamiel O. Gruber N, et al. J Adolesc Health. 2020 May;66(5):603-609. doi: 10.1016/j.jadohealth.2019.11.315. Epub 2020 Jan 25. J Adolesc Health. 2020. PMID: 31987720

8

Birth during the moderate weather seasons is associated with early onset of type 1 diabetes in the Mediterranean area.

Adar A, Shalitin S, Eyal O, Loewenthal N, Pinhas-Hamiel O, Zuckerman Levin N, Dally-Gottfried O, Landau Z, Zung A, Levy-Khademi F, Zangen D, Tenenbaum-Rakover Y, Rachmiel M. Adar A, et al. Diabetes Metab Res Rev. 2020 Oct;36(7):e3318. doi: 10.1002/dmrr.3318. Epub 2020 Apr 19. Diabetes Metab Res Rev. 2020. PMID: 32270907

9

Hyperandrogenism in carriers of CYP21 mutations: the role of genotype.

Admoni O, Israel S, Lavi I, Gur M, Tenenbaum-Rakover Y. Admoni O, et al. Clin Endocrinol (Oxf). 2006 Jun;64(6):645-51. doi: 10.1111/j.1365-2265.2006.02521.x. Clin Endocrinol (Oxf). 2006. PMID: 16712666

10

Congenital hyperreninemic hypoaldosteronism in Israel: sequence analysis of CYP11B2 gene.

Leshinsky-Silver E, Landau Z, Unlubay S, Bistrizer T, Zung A, Tenenbaum-Rakover Y, Devries L, Lev D, Hanukoglu A. Leshinsky-Silver E, et al. Horm Res. 2006;66(2):73-8. doi: 10.1159/000093583. Epub 2006 May 29. Horm Res. 2006. PMID: 16733366

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