Tenenbaum-Rakover Y - Search Results

1

Loss-of-function mutations in the thyrotropin receptor gene as a major determinant of hyperthyrotropinemia in a consanguineous community.

Tenenbaum-Rakover Y, Grasberger H, Mamanasiri S, Ringkananont U, Montanelli L, Barkoff MS, Dahood AM, Refetoff S. Tenenbaum-Rakover Y, et al. J Clin Endocrinol Metab. 2009 May;94(5):1706-12. doi: 10.1210/jc.2008-1938. Epub 2009 Feb 24. J Clin Endocrinol Metab. 2009. PMID: 19240155 Free PMC article.

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

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

4

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

5

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

6

A familial thyrotropin (TSH) receptor mutation provides in vivo evidence that the inositol phosphates/Ca2+ cascade mediates TSH action on thyroid hormone synthesis.

Grasberger H, Van Sande J, Hag-Dahood Mahameed A, Tenenbaum-Rakover Y, Refetoff S. Grasberger H, et al. J Clin Endocrinol Metab. 2007 Jul;92(7):2816-20. doi: 10.1210/jc.2007-0366. Epub 2007 Apr 24. J Clin Endocrinol Metab. 2007. PMID: 17456567

7

Variable phenotypes in familial isolated growth hormone deficiency caused by a G6664A mutation in the GH-1 gene.

Hess O, Hujeirat Y, Wajnrajch MP, Allon-Shalev S, Zadik Z, Lavi I, Tenenbaum-Rakover Y. Hess O, et al. J Clin Endocrinol Metab. 2007 Nov;92(11):4387-93. doi: 10.1210/jc.2007-0684. Epub 2007 Sep 4. J Clin Endocrinol Metab. 2007. PMID: 17785368

8

Control of childhood congenital adrenal hyperplasia and sleep activity and quality with morning or evening glucocorticoid therapy.

German A, Suraiya S, Tenenbaum-Rakover Y, Koren I, Pillar G, Hochberg Z. German A, et al. J Clin Endocrinol Metab. 2008 Dec;93(12):4707-10. doi: 10.1210/jc.2008-0519. Epub 2008 Sep 9. J Clin Endocrinol Metab. 2008. PMID: 18782876 Clinical Trial.

9

Neonatal hyperthyrotropinemia: population characteristics, diagnosis, management and outcome after cessation of therapy.

Zung A, Tenenbaum-Rakover Y, Barkan S, Hanukoglu A, Hershkovitz E, Pinhas-Hamiel O, Bistritzer T, Zadik Z. Zung A, et al. Clin Endocrinol (Oxf). 2010 Feb;72(2):264-71. doi: 10.1111/j.1365-2265.2009.03634.x. Epub 2009 May 18. Clin Endocrinol (Oxf). 2010. PMID: 19473184

10

A novel loss-of-function mutation, Gln459Arg, of the calcium-sensing receptor gene associated with apparent autosomal recessive inheritance of familial hypocalciuric hypercalcemia.

Lietman SA, Tenenbaum-Rakover Y, Jap TS, Yi-Chi W, De-Ming Y, Ding C, Kussiny N, Levine MA. Lietman SA, et al. J Clin Endocrinol Metab. 2009 Nov;94(11):4372-9. doi: 10.1210/jc.2008-2484. Epub 2009 Sep 29. J Clin Endocrinol Metab. 2009. PMID: 19789209 Free PMC article.

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