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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1995 1
1996 1
1997 1
2003 1
2005 1
2006 3
2007 2
2010 2
2011 1
2012 1
2015 2
2016 1
2017 1
2020 1
2021 1
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18 results
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Page 1
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.
Novel microdeletions affecting the GNAS locus in pseudohypoparathyroidism: characterization of the underlying mechanisms.
Garin I, Elli FM, Linglart A, Silve C, de Sanctis L, Bordogna P, Pereda A, Clarke JT, Kannengiesser C, Coutant R, Tenebaum-Rakover Y, Admoni O, de Nanclares GP, Mantovani G. Garin I, et al. Among authors: admoni o. J Clin Endocrinol Metab. 2015 Apr;100(4):E681-7. doi: 10.1210/jc.2014-3098. Epub 2015 Jan 16. J Clin Endocrinol Metab. 2015. PMID: 25594858 Free article.
Clinical significance of the parental origin of the X chromosome in turner syndrome.
Sagi L, Zuckerman-Levin N, Gawlik A, Ghizzoni L, Buyukgebiz A, Rakover Y, Bistritzer T, Admoni O, Vottero A, Baruch O, Fares F, Malecka-Tendera E, Hochberg Z. Sagi L, et al. Among authors: admoni o. J Clin Endocrinol Metab. 2007 Mar;92(3):846-52. doi: 10.1210/jc.2006-0158. Epub 2006 Dec 27. J Clin Endocrinol Metab. 2007. PMID: 17192299
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. Among authors: admoni o. 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.
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