Sezgin I - Search Results

1

Adult height in Turkish patients with Turner syndrome without growth hormone treatment.

Bereket A, Turan S, Elçioğlu N, Hacihanefioğlu S, Memioğlu N, Baş F, Bundak R, Darendeliler F, Günöz H, Saka N, Ercan O, Arslanoğlu I, Işgüven P, Yildiz M, Can S, Ozerkan E, Coker M, Darcan S, Ozkan B, Orbak Z, Oztaş S, Palandüz S, Sezgin I, Atabek E, Erkul I, Erdoğan G. Bereket A, et al. Among authors: sezgin i. Turk J Pediatr. 2008 Sep-Oct;50(5):415-7. Turk J Pediatr. 2008. PMID: 19102043

2

Meckel-gruber syndrome associated with gastrointestinal tractus anomaly.

Ergür AT, Taş F, Yildiz E, Kiliç F, Sezgin I. Ergür AT, et al. Among authors: sezgin i. Turk J Pediatr. 2004 Oct-Dec;46(4):388-92. Turk J Pediatr. 2004. PMID: 15641280

3

Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia.

Yildirim ME, Kurtulgan HK, Ozdemir O, Kilicgun H, Aydemir DS, Baser B, Sezgin I. Yildirim ME, et al. Among authors: sezgin i. Ann Saudi Med. 2019 Nov-Dec;39(6):382-387. doi: 10.5144/0256-4947.2019.382. Epub 2019 Dec 5. Ann Saudi Med. 2019. PMID: 31804137 Free PMC article.

4

The type and prevalence of chromosomal abnormalities in couples with recurrent first trimester abortions: A Turkish retrospective study.

Yildirim ME, Karakus S, Kurtulgan HK, Baser B, Sezgin I. Yildirim ME, et al. Among authors: sezgin i. J Gynecol Obstet Hum Reprod. 2019 Sep;48(7):521-525. doi: 10.1016/j.jogoh.2019.05.014. Epub 2019 May 11. J Gynecol Obstet Hum Reprod. 2019. PMID: 31085277

5

Dental findings in Cornelia de Lange syndrome.

Toker AS, Ay S, Yeler H, Sezgin I. Toker AS, et al. Among authors: sezgin i. Yonsei Med J. 2009 Apr 30;50(2):289-92. doi: 10.3349/ymj.2009.50.2.289. Yonsei Med J. 2009. PMID: 19430566 Free PMC article.

6

The protective effect of MCP-1 -2518 A>G promoter polymorphism in Turkish chronic renal failure patients requiring long-term hemodialysis.

Bagci B, Bagci G, Candan F, Ozdemir O, Sezgin I. Bagci B, et al. Among authors: sezgin i. Int Urol Nephrol. 2015 Mar;47(3):551-6. doi: 10.1007/s11255-015-0922-3. Epub 2015 Feb 6. Int Urol Nephrol. 2015. PMID: 25655256

7

Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers.

Ozdemir O, Sezgin I, Kurtulgan HK, Candan F, Koksal B, Sumer H, Icagasioglu D, Uslu A, Yildiz F, Arslan S, Cetinkaya S, Citli S, Oztemur Z, Kayatas M. Ozdemir O, et al. Among authors: sezgin i. Mol Biol Rep. 2011 Jun;38(5):3195-200. doi: 10.1007/s11033-010-9991-7. Epub 2010 Feb 18. Mol Biol Rep. 2011. PMID: 20165923

8

Noonan's syndrome with simple partial syndactyly of the fingers and bilateral cubital webs.

Undar L, Gultekin A, Yilmaz MB, Sezgin I. Undar L, et al. Among authors: sezgin i. Indian Pediatr. 1990 Nov;27(11):1220-2. Indian Pediatr. 1990. PMID: 1964444 No abstract available.

9

Larsen's syndrome with mixed-type hearing loss.

Perçín EF, Perçín S, Sezgin I, Akbas AK. Perçín EF, et al. Among authors: sezgin i. Acta Orthop Belg. 1994;60(3):328-31. Acta Orthop Belg. 1994. PMID: 7992613

10

The fetal hydantoin syndrome.

Oğuz A, Sezgin I, Gökalp A, Gültekin A. Oğuz A, et al. Among authors: sezgin i. Mater Med Pol. 1991 Oct-Dec;23(4):308-11. Mater Med Pol. 1991. PMID: 1842240 No abstract available.

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