Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1997 1
1999 2
2001 1
2002 6
2003 5
2004 6
2005 5
2006 7
2007 6
2008 9
2009 4
2010 6
2011 3
2012 2
2013 3
2014 4
2015 6
2016 4
2017 3
2018 2
2019 1
2020 1
2021 2
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

76 results

Results by year

Filters applied: . Clear all
Page 1
Familial adenomatous polyposis.
Half E, Bercovich D, Rozen P. Half E, et al. Among authors: bercovich d. Orphanet J Rare Dis. 2009 Oct 12;4:22. doi: 10.1186/1750-1172-4-22. Orphanet J Rare Dis. 2009. PMID: 19822006 Free PMC article. Review.
Fullerene and the origin of life.
Goodman G, Gershwin ME, Bercovich D. Goodman G, et al. Among authors: bercovich d. Isr Med Assoc J. 2012 Oct;14(10):602-6. Isr Med Assoc J. 2012. PMID: 23193780 Free article. Review.
Mammal domestication and the symbiotic spectrum.
Dekel Y, Machluf Y, Brand R, Noked Partouche O, Ben-Shlomo I, Bercovich D. Dekel Y, et al. Among authors: bercovich d. Proc Natl Acad Sci U S A. 2017 Jul 3;114(27):E5280. doi: 10.1073/pnas.1705784114. Epub 2017 Jun 13. Proc Natl Acad Sci U S A. 2017. PMID: 28611226 Free PMC article. No abstract available.
The many faces of Glut1 deficiency syndrome.
Tzadok M, Nissenkorn A, Porper K, Matot I, Marcu S, Anikster Y, Menascu S, Bercovich D, Ben Zeev B. Tzadok M, et al. Among authors: bercovich d. J Child Neurol. 2014 Mar;29(3):349-59. doi: 10.1177/0883073812471718. Epub 2013 Jan 22. J Child Neurol. 2014. PMID: 23340081
High Prevalence of Hearing Impairment in Primary Congenital Hypothyroidism.
Almagor T, Rath S, Nachtigal D, Sharroni Z, Elias-Assad G, Hess O, Havazelet G, Zehavi Y, Spiegel R, Bercovich D, Almashanu S, Tenenbaum-Rakover Y. Almagor T, et al. Among authors: bercovich d. Eur Thyroid J. 2021 Jun;10(3):215-221. doi: 10.1159/000509775. Epub 2020 Sep 3. Eur Thyroid J. 2021. PMID: 34178707 Free PMC article.
A novel heterozygous IGF-1 receptor mutation associated with hypoglycemia.
Solomon-Zemler R, Basel-Vanagaite L, Steier D, Yakar S, Mel E, Phillip M, Bazak L, Bercovich D, Werner H, de Vries L. Solomon-Zemler R, et al. Among authors: bercovich d. Endocr Connect. 2017 Aug;6(6):395-403. doi: 10.1530/EC-17-0038. Epub 2017 Jun 25. Endocr Connect. 2017. PMID: 28649085 Free PMC article.
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. Among authors: bercovich d. Thyroid. 2016 Dec;26(12):1693-1700. doi: 10.1089/thy.2015.0672. Epub 2016 Jul 25. Thyroid. 2016. PMID: 27310681
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: bercovich d. Thyroid. 2015 Mar;25(3):292-9. doi: 10.1089/thy.2014.0311. Epub 2015 Jan 28. Thyroid. 2015. PMID: 25557138 Free PMC article.
76 results