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

Year Number of Results
2003 2
2004 4
2009 2
2010 2
2011 2
2012 3
2013 2
2014 2
2015 4
2016 8
2017 1
2018 3
2020 1
2021 2
2022 2
2023 2
2024 0

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38 results

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Page 1
Molecular causes of hypogonadotropic hypogonadism.
Topaloglu AK, Kotan LD. Topaloglu AK, et al. Curr Opin Obstet Gynecol. 2010 Aug;22(4):264-70. doi: 10.1097/GCO.0b013e32833bb425. Curr Opin Obstet Gynecol. 2010. PMID: 20543690 Review.
Pathogenic Variants in ZSWIM7 Cause Primary Ovarian Insufficiency.
Yatsenko SA, Gurbuz F, Topaloglu AK, Berman AJ, Martin PM, Rodrigue-Escribà M, Qin Y, Rajkovic A. Yatsenko SA, et al. Among authors: topaloglu ak. J Clin Endocrinol Metab. 2022 May 17;107(6):e2359-e2364. doi: 10.1210/clinem/dgac090. J Clin Endocrinol Metab. 2022. PMID: 35218660 Free PMC article.
A novel homozygous nonsense NDNF variant in Kallmann syndrome.
Kotan LD, Yildiz M, Turan I, Celiloglu C, Yuksel B, Topaloglu AK. Kotan LD, et al. Among authors: topaloglu ak. Am J Med Genet A. 2023 Mar;191(3):831-834. doi: 10.1002/ajmg.a.63066. Epub 2022 Dec 1. Am J Med Genet A. 2023. PMID: 36454653
Sertoli cell only syndrome with ambiguous genitalia.
Gurbuz F, Ceylaner S, Erdogan S, Topaloglu AK, Yuksel B. Gurbuz F, et al. Among authors: topaloglu ak. J Pediatr Endocrinol Metab. 2016 Jul 1;29(7):849-52. doi: 10.1515/jpem-2015-0458. J Pediatr Endocrinol Metab. 2016. PMID: 27124672
Coexistence of Kabuki Syndrome and Autoimmune Thyroiditis.
Gürbüz F, Özalp Yüreğir Ö, Ceylaner S, Topaloğlu AK, Yüksel B. Gürbüz F, et al. Among authors: topaloglu ak. J Clin Res Pediatr Endocrinol. 2016 Mar 5;8(1):105-6. doi: 10.4274/jcrpe.2686. Epub 2015 Dec 18. J Clin Res Pediatr Endocrinol. 2016. PMID: 26757828 Free PMC article. No abstract available.
Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation.
Gürbüz F, Yüksel B, Topaloğlu AK. Gürbüz F, et al. Among authors: topaloglu ak. J Clin Res Pediatr Endocrinol. 2016 Dec 1;8(4):496-497. doi: 10.4274/jcrpe.3065. Epub 2016 Jun 4. J Clin Res Pediatr Endocrinol. 2016. PMID: 27145240 Free PMC article. No abstract available.
A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome.
Mengen E, Kotan LD, Ucakturk SA, Topaloglu AK, Yuksel B. Mengen E, et al. Among authors: topaloglu ak. J Coll Physicians Surg Pak. 2018 May;28(5):403-405. doi: 10.29271/jcpsp.2018.05.403. J Coll Physicians Surg Pak. 2018. PMID: 29690975
38 results