Coğulu O - Search Results

1

Oxidative stress biomarkers in four Bloom syndrome (BS) patients and in their parents suggest in vivo redox abnormalities in BS phenotype.

Zatterale A, Kelly FJ, Degan P, d'Ischia M, Pallardó FV, Calzone R, Dunster C, Lloret A, Manini P, Coğulu O, Kavakli K, Pagano G. Zatterale A, et al. Among authors: cogulu o. Clin Biochem. 2007 Oct;40(15):1100-3. doi: 10.1016/j.clinbiochem.2007.06.003. Epub 2007 Jun 30. Clin Biochem. 2007. PMID: 17678887

2

A case of primary chylous ascites resolved within 4 months by exclusive breast-feeding.

Kurugöl Z, Coğulu O, Kavakli K. Kurugöl Z, et al. Among authors: cogulu o. Turk J Pediatr. 2000 Apr-Jun;42(2):165-7. Turk J Pediatr. 2000. PMID: 10936987

3

A novel mutation in the DIA1 gene in a patient with methemoglobinemia type II.

Yilmaz D, Cogulu O, Ozkinay F, Kavakli K, Roos D. Yilmaz D, et al. Among authors: cogulu o. Am J Med Genet A. 2005 Feb 15;133A(1):101-2. doi: 10.1002/ajmg.a.30467. Am J Med Genet A. 2005. PMID: 15744830 No abstract available.

4

Prospective evaluation of whole genome microRNA expression profiling in childhood acute lymphoblastic leukemia.

Duyu M, Durmaz B, Gunduz C, Vergin C, Yilmaz Karapinar D, Aksoylar S, Kavakli K, Cetingul N, Irken G, Yaman Y, Ozkinay F, Cogulu O. Duyu M, et al. Among authors: cogulu o. Biomed Res Int. 2014;2014:967585. doi: 10.1155/2014/967585. Epub 2014 May 14. Biomed Res Int. 2014. PMID: 24955371 Free PMC article.

5

Micronucleus evaluation for determining the chromosomal breakages after radionuclide synovectomy in patients with hemophilia.

Kavakli K, Cogulu O, Karaca E, Durmaz B, Ozkinay F, Aydogdu S, Ozkilic H, Balkan C, Karapinar D, Ay Y. Kavakli K, et al. Among authors: cogulu o. Ann Nucl Med. 2012 Jan;26(1):41-6. doi: 10.1007/s12149-011-0540-9. Epub 2011 Oct 14. Ann Nucl Med. 2012. PMID: 21996780

6

Long-term evaluation of chromosomal breakages after radioisotope synovectomy for treatment of target joints in patients with haemophilia.

Kavakli K, Cogulu O, Aydogdu S, Ozkiliç H, Durmaz B, Kirbiyik O, Ozkinay F, Balkan C, Karapinar D, Ay Y. Kavakli K, et al. Among authors: cogulu o. Haemophilia. 2010 May;16(3):474-8. doi: 10.1111/j.1365-2516.2009.02167.x. Epub 2009 Dec 28. Haemophilia. 2010. PMID: 20050929

7

A new chromosomal rearrangement in acute myeloid leukemia.

Cetingül N, Oniz H, Coğulu O, Ozkinay F, Kavakli K, Kantar M, Aydinok Y, Polat A, Nişli G, Oztop S. Cetingül N, et al. Among authors: cogulu o. Cancer Genet Cytogenet. 1998 Dec;107(2):153-4. doi: 10.1016/s0165-4608(98)00093-4. Cancer Genet Cytogenet. 1998. PMID: 9844613 No abstract available.

8

A new patient with LACHT syndrome (Mardini-Nyhan association).

Atik T, Torun HO, Cogulu O, Ozkinay F. Atik T, et al. Among authors: cogulu o. Am J Med Genet A. 2015 Feb;167A(2):400-2. doi: 10.1002/ajmg.a.36832. Epub 2014 Dec 8. Am J Med Genet A. 2015. PMID: 25487726

9

A rare cause of syndromic short stature: 3M syndrome in three families.

Isik E, Arican D, Atik T, Ooi JE, Darcan S, Ozen S, Simsek Kiper PO, Utine E, Cogulu O, Ozkinay F. Isik E, et al. Among authors: cogulu o. Am J Med Genet A. 2021 Feb;185(2):461-468. doi: 10.1002/ajmg.a.61989. Epub 2020 Nov 30. Am J Med Genet A. 2021. PMID: 33258289

10

The missing "link": an autosomal recessive short stature syndrome caused by a hypofunctional XYLT1 mutation.

Schreml J, Durmaz B, Cogulu O, Keupp K, Beleggia F, Pohl E, Milz E, Coker M, Ucar SK, Nürnberg G, Nürnberg P, Kuhn J, Ozkinay F. Schreml J, et al. Among authors: cogulu o. Hum Genet. 2014 Jan;133(1):29-39. doi: 10.1007/s00439-013-1351-y. Epub 2013 Aug 27. Hum Genet. 2014. PMID: 23982343

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