Tenenbaum-Rakover Y - Search Results

1

Long-Term Outcome of Patients with TPO Mutations.

Tobias L, Elias-Assad G, Khayat M, Admoni O, Almashanu S, Tenenbaum-Rakover Y. Tobias L, et al. Among authors: tenenbaum rakover y. J Clin Med. 2021 Aug 30;10(17):3898. doi: 10.3390/jcm10173898. J Clin Med. 2021. PMID: 34501348 Free PMC article.

2

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

3

Neuroendocrine phenotype analysis in five patients with isolated hypogonadotropic hypogonadism due to a L102P inactivating mutation of GPR54.

Tenenbaum-Rakover Y, Commenges-Ducos M, Iovane A, Aumas C, Admoni O, de Roux N. Tenenbaum-Rakover Y, et al. J Clin Endocrinol Metab. 2007 Mar;92(3):1137-44. doi: 10.1210/jc.2006-2147. Epub 2006 Dec 12. J Clin Endocrinol Metab. 2007. PMID: 17164310

4

Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis.

Tenenbaum-Rakover Y, Mamanasiri S, Ris-Stalpers C, German A, Sack J, Allon-Shalev S, Pohlenz J, Refetoff S. Tenenbaum-Rakover Y, et al. Clin Endocrinol (Oxf). 2007 May;66(5):695-702. doi: 10.1111/j.1365-2265.2007.02804.x. Epub 2007 Mar 23. Clin Endocrinol (Oxf). 2007. PMID: 17381485

5

Can auxology, IGF-I and IGFBP-3 measurements followed by MRI and genetic tests replace GH stimulation tests in the diagnosis of GH deficiency in children?

Tenenbaum-Rakover Y, Hujeirat Y, Admoni O, Khayat M, Allon-Shalev S, Hess O. Tenenbaum-Rakover Y, et al. J Pediatr Endocrinol Metab. 2010 Apr;23(4):387-94. doi: 10.1515/jpem.2010.060. J Pediatr Endocrinol Metab. 2010. PMID: 20583544

6

The coexistence of a novel inactivating mutant thyrotropin receptor allele with two thyroid peroxidase mutations: a genotype-phenotype correlation.

Sriphrapradang C, Tenenbaum-Rakover Y, Weiss M, Barkoff MS, Admoni O, Kawthar D, Caltabiano G, Pardo L, Dumitrescu AM, Refetoff S. Sriphrapradang C, et al. J Clin Endocrinol Metab. 2011 Jun;96(6):E1001-6. doi: 10.1210/jc.2011-0127. Epub 2011 Apr 13. J Clin Endocrinol Metab. 2011. PMID: 21490078 Free PMC article.

7

Ghrelin and growth hormone secretagogue receptor (GHSR) genes are not commonly involved in growth or weight abnormalities in an Israeli pediatric population.

Hess O, Admoni O, Khayat M, Elias G, Almagor T, Shalev SA, Tenenbaum-Rakover Y. Hess O, et al. J Pediatr Endocrinol Metab. 2012;25(5-6):537-40. doi: 10.1515/jpem-2012-0044. J Pediatr Endocrinol Metab. 2012. PMID: 22876551

8

A novel mutation in IGFALS, c.380T>C (p.L127P), associated with short stature, delayed puberty, osteopenia and hyperinsulinaemia in two siblings: insights into the roles of insulin growth factor-1 (IGF1).

Hess O, Khayat M, Hwa V, Heath KE, Teitler A, Hritan Y, Allon-Shalev S, Tenenbaum-Rakover Y. Hess O, et al. Clin Endocrinol (Oxf). 2013 Dec;79(6):838-44. doi: 10.1111/cen.12200. Epub 2013 Apr 13. Clin Endocrinol (Oxf). 2013. PMID: 23488611

9

Trends in the incidence of type 1 diabetes among Jews and Arabs in Israel.

Blumenfeld O, Dichtiar R, Shohat T; Israel IDDM Registry Study Group (IIRSG). Blumenfeld O, et al. Pediatr Diabetes. 2014 Sep;15(6):422-7. doi: 10.1111/pedi.12101. Epub 2013 Nov 27. Pediatr Diabetes. 2014. PMID: 24283719

10

Long-term outcome of loss-of-function mutations in thyrotropin receptor gene.

Tenenbaum-Rakover Y, Almashanu S, Hess O, Admoni O, Hag-Dahood Mahameed A, Schwartz N, Allon-Shalev S, Bercovich D, Refetoff S. Tenenbaum-Rakover Y, et al. Thyroid. 2015 Mar;25(3):292-9. doi: 10.1089/thy.2014.0311. Epub 2015 Jan 28. Thyroid. 2015. PMID: 25557138 Free PMC article.

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