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

Year Number of Results
1990 2
1991 1
1993 1
2004 1
2005 1
2006 1
2007 2
2008 8
2009 8
2010 3
2011 12
2012 10
2013 5
2014 10
2015 12
2016 6
2017 10
2018 13
2019 23
2020 18
2021 17
2022 15
2023 2
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Page 1
Introduction.
Guran T, Flück CE. Guran T, et al. Horm Res Paediatr. 2021 Sep 28. doi: 10.1159/000519896. Online ahead of print. Horm Res Paediatr. 2021. PMID: 34583362 No abstract available.
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease.
Karaca E, Harel T, Pehlivan D, Jhangiani SN, Gambin T, Coban Akdemir Z, Gonzaga-Jauregui C, Erdin S, Bayram Y, Campbell IM, Hunter JV, Atik MM, Van Esch H, Yuan B, Wiszniewski W, Isikay S, Yesil G, Yuregir OO, Tug Bozdogan S, Aslan H, Aydin H, Tos T, Aksoy A, De Vivo DC, Jain P, Geckinli BB, Sezer O, Gul D, Durmaz B, Cogulu O, Ozkinay F, Topcu V, Candan S, Cebi AH, Ikbal M, Yilmaz Gulec E, Gezdirici A, Koparir E, Ekici F, Coskun S, Cicek S, Karaer K, Koparir A, Duz MB, Kirat E, Fenercioglu E, Ulucan H, Seven M, Guran T, Elcioglu N, Yildirim MS, Aktas D, Alikaşifoğlu M, Ture M, Yakut T, Overton JD, Yuksel A, Ozen M, Muzny DM, Adams DR, Boerwinkle E, Chung WK, Gibbs RA, Lupski JR. Karaca E, et al. Among authors: guran t. Neuron. 2015 Nov 4;88(3):499-513. doi: 10.1016/j.neuron.2015.09.048. Neuron. 2015. PMID: 26539891 Free PMC article.
Mutations in CYP24A1 and idiopathic infantile hypercalcemia.
Schlingmann KP, Kaufmann M, Weber S, Irwin A, Goos C, John U, Misselwitz J, Klaus G, Kuwertz-Bröking E, Fehrenbach H, Wingen AM, Güran T, Hoenderop JG, Bindels RJ, Prosser DE, Jones G, Konrad M. Schlingmann KP, et al. Among authors: guran t. N Engl J Med. 2011 Aug 4;365(5):410-21. doi: 10.1056/NEJMoa1103864. Epub 2011 Jun 15. N Engl J Med. 2011. PMID: 21675912 Free article.
Primary adrenal insufficiency in children: Diagnosis and management.
Kirkgoz T, Guran T. Kirkgoz T, et al. Among authors: guran t. Best Pract Res Clin Endocrinol Metab. 2018 Aug;32(4):397-424. doi: 10.1016/j.beem.2018.05.010. Epub 2018 Jun 6. Best Pract Res Clin Endocrinol Metab. 2018. PMID: 30086866 Review.
mTOR-Activating Mutations in RRAGD Are Causative for Kidney Tubulopathy and Cardiomyopathy.
Schlingmann KP, Jouret F, Shen K, Nigam A, Arjona FJ, Dafinger C, Houillier P, Jones DP, Kleinerüschkamp F, Oh J, Godefroid N, Eltan M, Güran T, Burtey S, Parotte MC, König J, Braun A, Bos C, Ibars Serra M, Rehmann H, Zwartkruis FJT, Renkema KY, Klingel K, Schulze-Bahr E, Schermer B, Bergmann C, Altmüller J, Thiele H, Beck BB, Dahan K, Sabatini D, Liebau MC, Vargas-Poussou R, Knoers NVAM, Konrad M, de Baaij JHF. Schlingmann KP, et al. Among authors: guran t. J Am Soc Nephrol. 2021 Nov;32(11):2885-2899. doi: 10.1681/ASN.2021030333. Epub 2021 Oct 4. J Am Soc Nephrol. 2021. PMID: 34607910 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: guran t. 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
Adrenal steroids reference ranges in infancy determined by LC-MS/MS.
Enver EO, Vatansever P, Guran O, Bilgin L, Boran P, Turan S, Haklar G, Bereket A, Guran T. Enver EO, et al. Among authors: guran t. Pediatr Res. 2022 Jul;92(1):265-274. doi: 10.1038/s41390-021-01739-5. Epub 2021 Sep 23. Pediatr Res. 2022. PMID: 34556810
A retrospective analysis of endocrine disease in sphingosine-1-phosphate lyase insufficiency: case series and literature review.
Maharaj A, Kwong R, Williams J, Smith C, Storr H, Krone R, Braslavsky D, Clemente M, Ram N, Banerjee I, Çetinkaya S, Buonocore F, Güran T, Achermann JC, Metherell L, Prasad R. Maharaj A, et al. Among authors: guran t. Endocr Connect. 2022 Jul 25;11(8):e220250. doi: 10.1530/EC-22-0250. Print 2022 Aug 1. Endocr Connect. 2022. PMID: 35904228 Free PMC article. Review.
144 results