Alpman A - Search Results

1

No relationship between lipoprotein-associated phospholipase A2, proinflammatory cytokines, and neopterin in Alzheimer's disease.

Savas S, Kabaroglu C, Alpman A, Sarac F, Yalcin MA, Parıldar Z, Ozkinay F, Kumral E, Akcicek F. Savas S, et al. Among authors: alpman a. Exp Gerontol. 2016 May;77:1-6. doi: 10.1016/j.exger.2016.01.014. Epub 2016 Jan 29. Exp Gerontol. 2016. PMID: 26828804

2

Association of interleukin-1beta and interleukin-1 receptor antagonist gene polymorphisms in Turkish children with atopic asthma.

Zeyrek D, Demir E, Alpman A, Ozkinay F, Gulen F, Tanac R. Zeyrek D, et al. Among authors: alpman a. Allergy Asthma Proc. 2008 Sep-Oct;29(5):468-74. doi: 10.2500/aap.2008.29.3154. Allergy Asthma Proc. 2008. PMID: 18926055

3

Multidrug resistance 1 (MDR1) gene polymorphisms in childhood drug-resistant epilepsy.

Alpman A, Ozkinay F, Tekgul H, Gokben S, Pehlivan S, Schalling M, Ozkinay C. Alpman A, et al. J Child Neurol. 2010 Dec;25(12):1485-90. doi: 10.1177/0883073810368997. Epub 2010 May 6. J Child Neurol. 2010. PMID: 20448249

4

Febrile seizures: interleukin 1beta and interleukin-1 receptor antagonist polymorphisms.

Serdaroğlu G, Alpman A, Tosun A, Pehlivan S, Ozkinay F, Tekgül H, Gökben S. Serdaroğlu G, et al. Among authors: alpman a. Pediatr Neurol. 2009 Feb;40(2):113-6. doi: 10.1016/j.pediatrneurol.2008.10.004. Pediatr Neurol. 2009. PMID: 19135625

5

Evaluation of the SMN and NAIP genes in a family: homozygous deletion of the SMN2 gene in the fetus and outcome of the pregnancy.

Cogulu O, Durmaz B, Pehlivan S, Alpman A, Ozkinay F. Cogulu O, et al. Among authors: alpman a. Genet Test Mol Biomarkers. 2009 Jun;13(3):287-8. doi: 10.1089/gtmb.2008.0139. Genet Test Mol Biomarkers. 2009. PMID: 19397406 No abstract available.

6

A new case of Martsolf syndrome.

Bora E, Cankaya T, Alpman A, Karaca E, Cogulu O, Tekgul H, Ozkinay F. Bora E, et al. Among authors: alpman a. Genet Couns. 2007;18(1):71-5. Genet Couns. 2007. PMID: 17515302

7

Chronic myelogenous leukemia exhibiting trisomy 14 due to a Robertsonian translocation with philadelphia chromosome.

Durmaz B, Karaca E, Vural F, Cogulu O, Alpman A, Tombuloglu M, Ozkinay F. Durmaz B, et al. Among authors: alpman a. Acta Oncol. 2008;47(8):1604-6. doi: 10.1080/02841860802078077. Acta Oncol. 2008. PMID: 18607844 No abstract available.

8

Trends in cytogenetic prenatal diagnosis in a reference hospital in Izmir/Turkey: a comparative study for four years.

Gunduz C, Cogulu O, Cankaya T, Bora E, Karaca E, Alpman A, Sagol S, Onay H, Ozkinay F, Ozkinay C. Gunduz C, et al. Among authors: alpman a. Genet Couns. 2004;15(1):53-9. Genet Couns. 2004. PMID: 15083700

9

The evaluation of the referral reasons of patients at a tertiary pediatric genetic center in Izmir, Turkey.

Durmaz B, Alpman A, Pariltay E, Akgul M, Ataman E, Kirbiyik O, Cogulu O, Ozkinay F. Durmaz B, et al. Among authors: alpman a. Genet Test Mol Biomarkers. 2009 Apr;13(2):163-6. doi: 10.1089/gtmb.2008.0074. Genet Test Mol Biomarkers. 2009. PMID: 19371213

10

Ring chromosome 20 syndrome with intractable epilepsy.

Alpman A, Serdaroglu G, Cogulu O, Tekgul H, Gokben S, Ozkinay F. Alpman A, et al. Dev Med Child Neurol. 2005 May;47(5):343-6. doi: 10.1017/s0012162205000642. Dev Med Child Neurol. 2005. PMID: 15892377 Free article.

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