Ciliv G - Search Results

1

Biochemical and molecular characterization of mutant hexosaminidase A in a Turkish family.

Sinici I, Ozkara HA, Topçu M, Ciliv G. Sinici I, et al. Among authors: ciliv g. Pediatr Int. 2003 Feb;45(1):16-22. doi: 10.1046/j.1442-200x.2003.01669.x. Pediatr Int. 2003. PMID: 12654063

2

Donor splice site mutation in intron 5 of the HEXA gene in a Turkish infant with Tay-Sachs disease.

Ozkara HA, Akerman BR, Ciliv G, Topçu M, Renda Y, Gravel RA. Ozkara HA, et al. Among authors: ciliv g. Hum Mutat. 1995;5(2):186-7. doi: 10.1002/humu.1380050216. Hum Mutat. 1995. PMID: 7749419 No abstract available.

3

Serum ribonuclease activity in the diagnosis of prostate cancer in men with serum prostate-specific antigen levels between 2.5 and 20 ng/mL.

Eskicorapci SY, Ozkara HA, Onder E, Akdogan B, Erkan I, Ciliv G, Ozen H. Eskicorapci SY, et al. Among authors: ciliv g. Clin Biochem. 2006 Apr;39(4):363-6. doi: 10.1016/j.clinbiochem.2005.11.020. Epub 2006 Jan 19. Clin Biochem. 2006. PMID: 16423339

4

Increased hexosaminidase activity in antipsychotic-induced extrapyramidal side effects: possible association with higher occurrence in bipolar disorder patients.

Tunca Z, Resmi H, Ozkara HA, Ciliv G, Celtikci B, Alptekin K, Ozerdem A, Akdede BK, Baykara B, Birsoy B, Ergor G. Tunca Z, et al. Among authors: ciliv g. Prog Neuropsychopharmacol Biol Psychiatry. 2008 Jul 1;32(5):1214-20. doi: 10.1016/j.pnpbp.2008.03.008. Epub 2008 Mar 20. Prog Neuropsychopharmacol Biol Psychiatry. 2008. PMID: 18436361

5

Tay-Sachs disease: a case report.

Arisoy AE, Ozden S, Ciliv G, Ozalp I. Arisoy AE, et al. Among authors: ciliv g. Turk J Pediatr. 1995 Jan-Mar;37(1):51-6. Turk J Pediatr. 1995. PMID: 7732608

6

Glycogen storage disease type Ia: frequency and clinical course in Turkish children.

Saltik IN, Ozen H, Ciliv G, Koçak N, Yüce A, Gürakan F, Dinler G. Saltik IN, et al. Among authors: ciliv g. Indian J Pediatr. 2000 Jul;67(7):497-501. doi: 10.1007/BF02760476. Indian J Pediatr. 2000. PMID: 10957834

7

Analysis of three mutations in Turkish children with Gaucher disease.

Gürakan F, Terzioğlu M, Koçak N, Yüce A, Ozen H, Ciliv G, Emre S. Gürakan F, et al. Among authors: ciliv g. J Inherit Metab Dis. 1999 Dec;22(8):947-8. doi: 10.1023/a:1005668230365. J Inherit Metab Dis. 1999. PMID: 10604154 No abstract available.

8

Histologic features of the liver in type Ia glycogen storage disease: comparative study between different age groups and consecutive biopsies.

Göğüş S, Koçak N, Ciliv G, Karabulut E, Akçören Z, Kale G, Cağlar M. Göğüş S, et al. Among authors: ciliv g. Pediatr Dev Pathol. 2002 May-Jun;5(3):299-304. doi: 10.1007/s10024-001-0139-6. Pediatr Dev Pathol. 2002. PMID: 12007023

9

Glucose-6-phosphatase gene mutations in Turkish patients with glycogen storage disease type Ia.

Terzioglu M, Emre S, Ozen H, Saltik IN, Koçak N, Ciliv G, Yüce A, Gürakan F. Terzioglu M, et al. Among authors: ciliv g. J Inherit Metab Dis. 2001 Dec;24(8):881-2. doi: 10.1023/a:1013956611607. J Inherit Metab Dis. 2001. PMID: 11916325 No abstract available.

10

Breast milk beta-glucuronidase levels in hyperbilirubinemia.

Yiğit S, Ciliv G, Aygün C, Erdem G. Yiğit S, et al. Among authors: ciliv g. Turk J Pediatr. 2001 Apr-Jun;43(2):118-20. Turk J Pediatr. 2001. PMID: 11432488

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