Alikasifoglu M - Search Results

1

FTO gene-lifestyle interactions on serum adiponectin concentrations and central obesity in a Turkish population.

Isgin-Atici K, Alsulami S, Turan-Demirci B, Surendran S, Sendur SN, Lay I, Karabulut E, Ellahi B, Lovegrove JA, Alikasifoglu M, Erbas T, Vimaleswaran KS, Buyuktuncer Z. Isgin-Atici K, et al. Among authors: alikasifoglu m. Int J Food Sci Nutr. 2021 May;72(3):375-385. doi: 10.1080/09637486.2020.1802580. Epub 2020 Aug 4. Int J Food Sci Nutr. 2021. PMID: 32746650

2

Effects of angiotensin-converting enzyme gene polymorphism on the left-ventricular function and mass in patients with acromegaly.

Erbas T, Alikasifoglu M, Aksöyek S, Unsal I, Gedik O, Tuncbilek E. Erbas T, et al. Among authors: alikasifoglu m. Cardiology. 1999;92(4):226-31. doi: 10.1159/000006978. Cardiology. 1999. PMID: 10844381 Clinical Trial.

3

Thermolabile methylenetetrahydrofolate reductase enzyme genotype is frequent in type 2 diabetic patients with normal fasting homocysteine levels.

Tutuncu NB, Erbas T, Alikasifoglu M, Tuncbilek E. Tutuncu NB, et al. Among authors: alikasifoglu m. J Intern Med. 2005 May;257(5):446-53. doi: 10.1111/j.1365-2796.2005.01480.x. J Intern Med. 2005. PMID: 15836661 Free article.

4

Analysis of MTHFR 1298A>C in addition to MTHFR 677C>T polymorphism as a risk factor for neural tube defects in the Turkish population.

Boduroğlu K, Alanay Y, Alikaşifoğlu M, Aktaş D, Tunçbilek E. Boduroğlu K, et al. Among authors: alikasifoglu m. Turk J Pediatr. 2005 Oct-Dec;47(4):327-33. Turk J Pediatr. 2005. PMID: 16363341

5

Factor V Leiden mutation and type 1 diabetes mellitus.

Demirer AN, Alikasifoglu M, Tuncbilek E, Karakus S, Erbas T. Demirer AN, et al. Among authors: alikasifoglu m. Blood Coagul Fibrinolysis. 2008 Jan;19(1):70-4. doi: 10.1097/MBC.0b013e3282f38c5f. Blood Coagul Fibrinolysis. 2008. PMID: 18180619

6

Impact of renin-angiotensin system polymorphisms on renal haemodynamic responsiveness to acute angiotensin-converting enzyme inhibition in type 2 diabetes mellitus.

Volkan-Salanci B, Dagdelen S, Alikasifoglu M, Erbas T, Hayran M, Erbas B. Volkan-Salanci B, et al. Among authors: alikasifoglu m. J Renin Angiotensin Aldosterone Syst. 2009 Mar;10(1):41-50. doi: 10.1177/1470320309102326. J Renin Angiotensin Aldosterone Syst. 2009. PMID: 19286758 Free article. Clinical Trial.

7

Association between ACE and AGT polymorphism and cardiovascular risk in acromegalic patients.

Erbas T, Cinar N, Dagdelen S, Gedik A, Yorgun H, Canpolat U, Kabakci G, Alikasifoglu M. Erbas T, et al. Among authors: alikasifoglu m. Pituitary. 2017 Oct;20(5):569-577. doi: 10.1007/s11102-017-0819-5. Pituitary. 2017. PMID: 28712073

8

Unusual presentations of Carney Complex in patient with a novel PRKAR1A mutation.

Akin S, Noyan S, Dagdelen S, Pasaoglu I, Kaynaroglu V, Askun MM, Bilen CY, Kiratli H, Baydar DE, Onder S, Sokmensuer C, Aytemir K, Erkin G, Kiratli PO, Alikasifoglu M, Erbas T. Akin S, et al. Among authors: alikasifoglu m. Neuro Endocrinol Lett. 2017 Aug;38(4):248-254. Neuro Endocrinol Lett. 2017. PMID: 28871709

9

A case of Woodhouse-Sakati syndrome with pituitary iron deposition, cardiac and intestinal anomalies, with a novel mutation in DCAF17.

Sendur SN, Oguz S, Utine GE, Dagdelen S, Oguz KK, Erbas T, Alikasifoglu M. Sendur SN, et al. Among authors: alikasifoglu m. Eur J Med Genet. 2019 Aug;62(8):103687. doi: 10.1016/j.ejmg.2019.103687. Epub 2019 May 29. Eur J Med Genet. 2019. PMID: 31152917

10

Clock gene PERIOD3 polymorphism is associated with susceptibility to Graves' disease but not to Hashimoto's thyroiditis.

Helvaci N, Oguz SH, Kabacam S, Karabulut E, Akbiyik F, Alikasifoglu M, Gurlek A. Helvaci N, et al. Among authors: alikasifoglu m. Chronobiol Int. 2019 Oct;36(10):1343-1350. doi: 10.1080/07420528.2019.1642909. Epub 2019 Jul 22. Chronobiol Int. 2019. PMID: 31328557

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