Arman A - Search Results

1

Assessment of interleukin-1 gene cluster polymorphisms in lone atrial fibrillation: new insight into the role of inflammation in atrial fibrillation.

Gungor B, Ekmekci A, Arman A, Ozcan KS, Ucer E, Alper AT, Calik N, Yilmaz H, Tezel T, Coker A, Bolca O. Gungor B, et al. Among authors: arman a. Pacing Clin Electrophysiol. 2013 Oct;36(10):1220-7. doi: 10.1111/pace.12182. Epub 2013 May 28. Pacing Clin Electrophysiol. 2013. PMID: 23713812 Clinical Trial.

2

The effect of growth hormone on motor findings and dendrite morphology in an experimental Parkinson's disease model.

Kirazli O, Ozkan M, Verimli U, Gulhan R, Arman A, Sehirli US. Kirazli O, et al. Among authors: arman a. Anat Sci Int. 2024 Jul 31. doi: 10.1007/s12565-024-00790-6. Online ahead of print. Anat Sci Int. 2024. PMID: 39085683

3

Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty.

Kırkgöz T, Kaygusuz SB, Alavanda C, Helvacıoğlu D, Abalı ZY, Tosun BG, Eltan M, Menevşe TS, Guran T, Arman A, Turan S, Bereket A. Kırkgöz T, et al. Among authors: arman a. J Pediatr Endocrinol Metab. 2023 Mar 9;36(4):401-408. doi: 10.1515/jpem-2022-0645. Print 2023 Apr 25. J Pediatr Endocrinol Metab. 2023. PMID: 36883204

4

Interleukin-1 receptor antagonist (IL-1RN) and interleukin-1B gene polymorphisms in Turkish patients with rheumatoid arthritis.

Arman A, Yilmaz B, Coker A, Inanc N, Direskeneli H. Arman A, et al. Clin Exp Rheumatol. 2006 Nov-Dec;24(6):643-8. Clin Exp Rheumatol. 2006. PMID: 17207379

5

Interleukin-1B (-511) gene polymorphism is associated with acute coronary syndrome in the Turkish population.

Soylu O, Yildirim A, Coker A, Tezel T, List EO, Arman A. Soylu O, et al. Among authors: arman a. Eur Cytokine Netw. 2008 Mar;19(1):42-8. doi: 10.1684/ecn.2008.0119. Epub 2008 Feb 26. Eur Cytokine Netw. 2008. PMID: 18299273 Free article.

6

Novel splice site mutation in the growth hormone receptor gene in Turkish patients with Laron-type dwarfism.

Arman A, Ozon A, Isguven PS, Coker A, Peker I, Yordam N. Arman A, et al. J Pediatr Endocrinol Metab. 2008 Jan;21(1):47-58. doi: 10.1515/jpem.2008.21.1.47. J Pediatr Endocrinol Metab. 2008. PMID: 18404972

7

Interleukin-1 receptor antagonist gene VNTR polymorphism is associated with coronary artery disease.

Arman A, Soylu O, Yildirim A, Furman A, Ercelen N, Aydogan H, Coker A, Tezel T. Arman A, et al. Arq Bras Cardiol. 2008 Nov;91(5):293-8. doi: 10.1590/s0066-782x2008001700002. Arq Bras Cardiol. 2008. PMID: 19142372 Free article. English, Portuguese.

8

Characterization of GH-1 mutations in children with isolated growth hormone deficiency in the Turkish population.

Coker A, Cetinkaya E, Dundar B, Siklar Z, Buyukgebiz A, Arman A. Coker A, et al. Among authors: arman a. J Pediatr Endocrinol Metab. 2009 Oct;22(10):937-46. doi: 10.1515/jpem.2009.22.10.937. J Pediatr Endocrinol Metab. 2009. PMID: 20020582

9

Association between sporadic Parkinson disease and interleukin-1 beta -511 gene polymorphisms in the Turkish population.

Arman A, Isik N, Coker A, Candan F, Becit KS, List EO. Arman A, et al. Eur Cytokine Netw. 2010 Jun;21(2):116-21. doi: 10.1684/ecn.2010.0186. Epub 2010 Apr 28. Eur Cytokine Netw. 2010. PMID: 20427258 Free article.

10

Novel growth hormone receptor gene mutation in a patient with Laron syndrome.

Arman A, Yüksel B, Coker A, Sarioz O, Temiz F, Topaloglu AK. Arman A, et al. J Pediatr Endocrinol Metab. 2010 Apr;23(4):407-14. doi: 10.1515/jpem.2010.064. J Pediatr Endocrinol Metab. 2010. PMID: 20583548

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