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

Year Number of Results
1995 1
2001 1
2002 1
2003 2
2004 2
2005 3
2006 6
2007 6
2008 6
2009 6
2010 9
2011 8
2012 8
2013 9
2014 14
2015 19
2016 20
2017 20
2018 15
2019 24
2020 27
2021 31
2022 22
2023 16
2024 7

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238 results

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Page 1
Bi-allelic loss-of-function OBSCN variants predispose individuals to severe recurrent rhabdomyolysis.
Cabrera-Serrano M, Caccavelli L, Savarese M, Vihola A, Jokela M, Johari M, Capiod T, Madrange M, Bugiardini E, Brady S, Quinlivan R, Merve A, Scalco R, Hilton-Jones D, Houlden H, Aydin HI, Ceylaner S, Drewes S, Vockley J, Taylor RL, Folland C, Kelly A, Goullee H, Ylikallio E, Auranen M, Tyynismaa H, Udd B, Forrest ARR, Davis MR, Bratkovic D, Manton N, Robertson T, O'Gorman C, McCombe P, Laing NG, Phillips L, de Lonlay P, Ravenscroft G. Cabrera-Serrano M, et al. Among authors: ceylaner s. Brain. 2022 Nov 21;145(11):3985-3998. doi: 10.1093/brain/awab484. Brain. 2022. PMID: 34957489 Free article.
Vici syndrome in siblings born to consanguineous parents.
Tasdemir S, Sahin I, Cayır A, Yuce I, Ceylaner S, Tatar A. Tasdemir S, et al. Among authors: ceylaner s. Am J Med Genet A. 2016 Jan;170A(1):220-5. doi: 10.1002/ajmg.a.37398. Epub 2015 Sep 23. Am J Med Genet A. 2016. PMID: 26395118 Review.
Cystinosis in Eastern Turkey.
Doğan M, Bulan K, Kaba S, Cesur Y, Ceylaner S, Ustyol L. Doğan M, et al. Among authors: ceylaner s. J Pediatr Endocrinol Metab. 2016 Aug 1;29(8):965-9. doi: 10.1515/jpem-2014-0477. J Pediatr Endocrinol Metab. 2016. PMID: 27269891
Hb Andrew-Minneapolis Variant in a Turkish Family.
Sümter H, Mızrak S, Ceylaner S, Canatan D. Sümter H, et al. Among authors: ceylaner s. Turk J Haematol. 2023 Aug 31;40(3):234-235. doi: 10.4274/tjh.galenos.2023.2023-0239. Epub 2023 Jul 31. Turk J Haematol. 2023. PMID: 37519109 Free PMC article. No abstract available.
238 results