Admoni O - 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. Among authors: admoni o. 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. Among authors: admoni o. 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. Among authors: admoni o. 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. Among authors: admoni o. 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. Among authors: admoni o. 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

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. Among authors: admoni o. 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.

8

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.

9

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: admoni o. J Clin Med. 2021 Aug 30;10(17):3898. doi: 10.3390/jcm10173898. J Clin Med. 2021. PMID: 34501348 Free PMC article.

10

Youth-onset type 2 diabetes in Israel: A national cohort.

Zuckerman Levin N, Cohen M, Phillip M, Tenenbaum A, Koren I, Tenenbaum-Rakover Y, Admoni O, Hershkovitz E, Haim A, Mazor Aronovitch K, Zangen D, Strich D, Brener A, Yeshayahu Y, Schon Y, Rachmiel M, Ben-Ari T, Levy-Khademi F, Tibi R, Weiss R, Lebenthal Y, Pinhas-Hamiel O, Shehadeh N. Zuckerman Levin N, et al. Among authors: admoni o. Pediatr Diabetes. 2022 Sep;23(6):649-659. doi: 10.1111/pedi.13351. Epub 2022 Jun 1. Pediatr Diabetes. 2022. PMID: 35521999

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