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

Year Number of Results
1968 1
1969 1
1970 4
1971 2
1972 4
1973 2
1974 2
1975 2
1977 3
1978 2
1981 1
1983 1
1984 1
1985 2
1986 1
1988 1
1989 1
1990 6
1993 1
1994 2
1998 2
1999 2
2001 2
2002 3
2003 2
2004 3
2005 2
2009 1
2011 7
2012 6
2013 2
2014 4
2015 9
2016 6
2017 3
2018 6
2019 6
2020 4
2021 2
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98 results
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Page 1
Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey.
Eren E, Törel Ergür A, İşgüven ŞP, Çelebi Bitkin E, Berberoğlu M, Şıklar Z, Baş F, Yel S, Baş S, Söbü E, Bereket A, Turan S, Sağlam H, Atay Z, Ercan O, Güran T, Atabek ME, Korkmaz HA, Kılınç Uğurlu A, Akıncı A, Döğer E, Şimşek E, Akbaş ED, Abacı A, Gül Ü, Acar S, Mengen Uçaktürk E, Yıldız M, Ünal E, Tarım Ö. Eren E, et al. Among authors: atay z. J Clin Res Pediatr Endocrinol. 2019 May 28;11(2):149-156. doi: 10.4274/jcrpe.galenos.2018.2018.0206. Epub 2018 Nov 5. J Clin Res Pediatr Endocrinol. 2019. PMID: 30396878 Free PMC article.
Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease.
Jolly A, Bayram Y, Turan S, Aycan Z, Tos T, Abali ZY, Hacihamdioglu B, Coban Akdemir ZH, Hijazi H, Bas S, Atay Z, Guran T, Abali S, Bas F, Darendeliler F, Colombo R, Barakat TS, Rinne T, White JJ, Yesil G, Gezdirici A, Gulec EY, Karaca E, Pehlivan D, Jhangiani SN, Muzny DM, Poyrazoglu S, Bereket A, Gibbs RA, Posey JE, Lupski JR. Jolly A, et al. Among authors: atay z. J Clin Endocrinol Metab. 2019 Aug 1;104(8):3049-3067. doi: 10.1210/jc.2019-00248. J Clin Endocrinol Metab. 2019. PMID: 31042289 Free PMC article.
Revisiting Classical 3β-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases.
Guran T, Kara C, Yildiz M, Bitkin EC, Haklar G, Lin JC, Keskin M, Barnard L, Anik A, Catli G, Guven A, Kirel B, Tutunculer F, Onal H, Turan S, Akcay T, Atay Z, Yilmaz GC, Mamadova J, Akbarzade A, Sirikci O, Storbeck KH, Baris T, Chung BC, Bereket A. Guran T, et al. Among authors: atay z. J Clin Endocrinol Metab. 2020 Mar 1;105(3):dgaa022. doi: 10.1210/clinem/dgaa022. J Clin Endocrinol Metab. 2020. PMID: 31950145
Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort.
Guran T, Buonocore F, Saka N, Ozbek MN, Aycan Z, Bereket A, Bas F, Darcan S, Bideci A, Guven A, Demir K, Akinci A, Buyukinan M, Aydin BK, Turan S, Agladioglu SY, Atay Z, Abali ZY, Tarim O, Catli G, Yuksel B, Akcay T, Yildiz M, Ozen S, Doger E, Demirbilek H, Ucar A, Isik E, Ozhan B, Bolu S, Ozgen IT, Suntharalingham JP, Achermann JC. Guran T, et al. Among authors: atay z. J Clin Endocrinol Metab. 2016 Jan;101(1):284-92. doi: 10.1210/jc.2015-3250. Epub 2015 Nov 2. J Clin Endocrinol Metab. 2016. PMID: 26523528 Free PMC article.
Clinical Significance of Hypophosphatasemia in Children.
Bayramli R, Cevlik T, Guran T, Atay Z, Bas S, Haklar G, Bereket A, Turan S. Bayramli R, et al. Among authors: atay z. Calcif Tissue Int. 2020 Jun;106(6):608-615. doi: 10.1007/s00223-020-00677-4. Epub 2020 Feb 22. Calcif Tissue Int. 2020. PMID: 32088736
Hereditary vitamin D-resistant rickets: a report of four cases with two novel variants in the VDR gene and successful use of intermittent intravenous calcium via a peripheral route.
Abalı S, Tamura M, Turan S, Atay Z, Isguven P, Güran T, Haliloglu B, Baş S, Isojima T, Kitanaka S, Bereket A. Abalı S, et al. Among authors: atay z. J Pediatr Endocrinol Metab. 2020 Apr 28;33(4):557-562. doi: 10.1515/jpem-2019-0466. J Pediatr Endocrinol Metab. 2020. PMID: 32049653
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