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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

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76 results

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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
76 results