Deren O - Search Results

1

Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia.

Uz E, Alanay Y, Aktas D, Vargel I, Gucer S, Tuncbilek G, von Eggeling F, Yilmaz E, Deren O, Posorski N, Ozdag H, Liehr T, Balci S, Alikasifoglu M, Wollnik B, Akarsu NA. Uz E, et al. Among authors: deren o. Am J Hum Genet. 2010 May 14;86(5):789-96. doi: 10.1016/j.ajhg.2010.04.002. Epub 2010 May 6. Am J Hum Genet. 2010. PMID: 20451171 Free PMC article.

2

Prenatal echocardiographic diagnosis of congenital heart disease: comparison of past and current results.

Ozkutlu S, Ayabakan C, Karagöz T, Onderoğlu L, Deren O, Cağlar M, Güçer S. Ozkutlu S, et al. Among authors: deren o. Turk J Pediatr. 2005 Jul-Sep;47(3):232-8. Turk J Pediatr. 2005. PMID: 16250307

3

Prenatally diagnosed lethal type Larsen-like syndrome associated with bifid tongue.

Orhan D, Balci S, Deren O, Utine EG, Başaran A, Kale G. Orhan D, et al. Among authors: deren o. Turk J Pediatr. 2008 Jul-Aug;50(4):395-9. Turk J Pediatr. 2008. PMID: 19014058

4

Prenatal echocardiographic diagnosis of cardiac right/left axis and malpositions according to standardized Cordes technique.

Ozkutlu S, Bostan OM, Deren O, Onderoğlu L, Kale G, Güçer S, Orhan D. Ozkutlu S, et al. Among authors: deren o. Anadolu Kardiyol Derg. 2011 Mar;11(2):131-6. doi: 10.5152/akd.2011.033. Epub 2011 Feb 8. Anadolu Kardiyol Derg. 2011. PMID: 21303758

5

Cyclooxygenase immunohistochemical staining in the human ductus arteriosus after 24 weeks of gestational age.

Basaran A, Gyimadu A, Güçer Ş, Deren Ö. Basaran A, et al. Among authors: deren o. J Obstet Gynaecol. 2012 Feb;32(2):120-3. doi: 10.3109/01443615.2011.618892. J Obstet Gynaecol. 2012. PMID: 22296418

6

Fetal Mediastinal Fibrosarcoma. Report of Two Cases.

Cagan M, Yildirim S, Turkmen GG, Ozyuncu O, Akcoren Z, Deren O, Gucer S. Cagan M, et al. Among authors: deren o. Fetal Pediatr Pathol. 2022 Oct;41(5):843-851. doi: 10.1080/15513815.2021.1988010. Epub 2021 Oct 8. Fetal Pediatr Pathol. 2022. PMID: 34622726

7

A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis.

Besbas N, Draaken M, Ludwig M, Deren O, Orhan D, Bilginer Y, Ozaltin F. Besbas N, et al. Among authors: deren o. Eur J Pediatr. 2009 Dec;168(12):1449-54. doi: 10.1007/s00431-009-0945-9. Epub 2009 Feb 24. Eur J Pediatr. 2009. PMID: 19238435

8

A lethal and rare cause of arthrogryposis: Glyt1 encephalopathy.

Daşar T, Şimşek-Kiper PÖ, Taşkıran EZ, Çağan M, Özyüncü Ö, Deren Ö, Utine GE, Güçer KŞ, Boduroğlu K. Daşar T, et al. Among authors: deren o. Eur J Med Genet. 2022 Dec;65(12):104631. doi: 10.1016/j.ejmg.2022.104631. Epub 2022 Oct 3. Eur J Med Genet. 2022. PMID: 36195292

9

A new splenic artery Doppler velocimetric index for prediction of severe fetal anemia associated with Rh alloimmunization.

Bahado-Singh R, Oz U, Deren O, Pirhonen J, Kovanci E, Copel J, Onderoglu L. Bahado-Singh R, et al. Among authors: deren o. Am J Obstet Gynecol. 1999 Jan;180(1 Pt 1):49-54. doi: 10.1016/s0002-9378(99)70148-1. Am J Obstet Gynecol. 1999. PMID: 9914577 Free article.

10

Middle cerebral artery Doppler velocimetric deceleration angle as a predictor of fetal anemia in Rh-alloimmunized fetuses without hydrops.

Bahado-Singh RO, Oz AU, Hsu C, Kovanci E, Deren O, Onderoglu L, Mari G. Bahado-Singh RO, et al. Among authors: deren o. Am J Obstet Gynecol. 2000 Sep;183(3):746-51. doi: 10.1067/mob.2000.106818. Am J Obstet Gynecol. 2000. PMID: 10992203 Free article.

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