Tenenbaum-Rakover Y - Search Results

1

The evolving role of whole-exome sequencing in the management of disorders of sex development.

Tenenbaum-Rakover Y, Admoni O, Elias-Assad G, London S, Noufi-Barhoum M, Ludar H, Almagor T, Zehavi Y, Sultan C, Bertalan R, Bashamboo A, McElreavey K. Tenenbaum-Rakover Y, et al. Endocr Connect. 2021 Jun 16;10(6):620-629. doi: 10.1530/EC-21-0019. Endocr Connect. 2021. PMID: 34009138 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

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

5

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

6

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.

7

Familial Central Hypothyroidism Caused by a Novel IGSF1 Gene Mutation.

Tenenbaum-Rakover Y, Turgeon MO, London S, Hermanns P, Pohlenz J, Bernard DJ, Bercovich D. Tenenbaum-Rakover Y, et al. Thyroid. 2016 Dec;26(12):1693-1700. doi: 10.1089/thy.2015.0672. Epub 2016 Jul 25. Thyroid. 2016. PMID: 27310681

8

Persistent Müllerian Duct Syndrome Caused by a Novel Mutation of an Anti-MüIlerian Hormone Receptor Gene: Case Presentation and Literature Review.

Elias-Assad G, Elias M, Kanety H, Pressman A, Tenenbaum-Rakover Y. Elias-Assad G, et al. Pediatr Endocrinol Rev. 2016 Jun;13(4):731-40. Pediatr Endocrinol Rev. 2016. PMID: 27464416 Review.

9

A novel HSD17B3 gene mutation in a 46,XY female-phenotype newborn identified by whole-exome sequencing.

Bertalan R, Admoni O, Bashamboo A, Tenenbaum-Rakover Y, McElreavey K. Bertalan R, et al. Clin Endocrinol (Oxf). 2017 Oct;87(4):407-408. doi: 10.1111/cen.13396. Epub 2017 Jul 24. Clin Endocrinol (Oxf). 2017. PMID: 28617986 No abstract available.

10

Long-Term Follow-Up and Outcomes of Autoimmune Thyroiditis in Childhood.

Admoni O, Rath S, Almagor T, Elias-Assad G, Tenenbaum-Rakover Y. Admoni O, et al. Front Endocrinol (Lausanne). 2020 Jun 5;11:309. doi: 10.3389/fendo.2020.00309. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32582023 Free PMC article.

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