Search Results - "Karkucak, M"

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  1. 1

    Assessment of hand function and disability in fibromyalgia by Devrimsel, G., Turkyilmaz, A. K., Beyazal, M. S., Karkucak, M.

    Published in Zeitschrift für Rheumatologie (01-11-2019)
    “…Objective Fibromyalgia, a potentially debilitating chronic pain syndrome, is a chronic disease. We aimed to compare the hand function of fibromyalgia (FM)…”
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    Journal Article
  2. 2

    Sexual function in male patients with ankylosing spondylitis by Özkorumak, E, Karkucak, M, Civil, F, Tiryaki, A, Özden, G

    “…Sexuality is an important part of healthy life. Patients with ankylosing spondylitis (AS) may be vulnerable to sexual problems because of disease activity and…”
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  3. 3

    SRY-negative XX sex reversal in an English Cocker Spaniel: a case report by Nak, D., Gulten, T., Karkucak, M., Yilmaz, R., Nak, Y., Simsek, G., Shahzad, A.H.

    Published in Veterinární medicína (01-01-2015)
    “…A SRY-negative XX male describes a female karyotype with testicular tissue resulting from abnormal gonadal development. In such cases male gonad formation…”
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  4. 4

    The prevalence and risk factors of low back pain in the eastern Black Sea region of Turkey by Capkin, E, Karkucak, M, Cakırbay, H, Topbas, M, Karaca, A, Köse, M M, Gökmen, F

    “…Low back pain (LBP) is a public health problem commonly seen in all societies. The aim of this study was to determine the prevalence and specific risk factors…”
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    Polymorphisms of glutathione-s-transferase M1, T1, and P1 genes in endometrial carcinoma by Ozerkan, K, Atalay, M A, Yakut, T, Doster, Y, Yilmaz, E, Karkucak, M

    “…To investigate the polymorphism rates and possible roles of glutathione-s-transferase M1, T1, and P1 gene polymorphisms in the predisposition to endometrial…”
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  7. 7

    Polymorphisms in angiotensin-converting enzyme and glutathione s-transferase genes in Turkish population and risk for preeclampsia by Atalay, M A, Ozerkan, K, Karkucak, M, Yakut, T, Atik, Y, Develioglu, O H

    “…This study was conducted to investigate whether insertion/deletion (I/D) polymorphism of angiotensin-converting enzyme (ACE) gene and polymorphisms in…”
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  8. 8

    Ultrasonographic evaluation of femoral cartilage thickness in patients with ankylosing spondylitis by Batmaz, I, Kara, M, Tiftik, T, Çapkin, E, Karkucak, M, Serdar, Ö F, Kartal, F, Sariyildiz, M A, Özçakar, L

    Published in West Indian medical journal (01-08-2014)
    “…To evaluate femoral cartilage thickness in patients with ankylosing spondylitis (AS) by using ultrasonography. Eighty-four patients (55 M, 29 F) with a…”
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  9. 9

    Lack of association of ACE gene I/D polymorphism with obstructive sleep apnea syndrome in Turkish patients by Yakut, T, Karkucak, M, Ursavas, A, Gulten, T, Burgazlioglu, B, Gorukmez, O, Karadag, M

    Published in Genetics and molecular research (01-01-2010)
    “…Angiotensin-converting enzyme (ACE) is a vital enzyme in the renin-angiotensin-aldosterone system, and there are reports in the literature describing its role…”
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  10. 10

    Another small supernumerary marker chromosome derived from chromosome 9 in a Klinefelter patient by Gulten, T, Gorukmez, O, Karkucak, M, Ture, M, Yakut, T

    Published in West Indian medical journal (01-12-2012)
    “…Marker chromosomes are very rare in Klinefelter patients and phenotypic findings are related to the affected chromosomal region. The phenotypic effects of…”
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  11. 11

    Lack of association of genetic polymorphisms of angiotensin-converting enzyme gene I/D and glutathione-S-transferase enzyme T1 and M1 with retinopathy of prematures by Yildiz, M, Karkucak, M, Yakut, T, Gorukmez, O, Ozmen, A

    Published in Genetics and molecular research (01-01-2010)
    “…One of the most frequently observed causes of blindness in infancy is the pathogenesis known as retinopathy of prematurity (ROP). Angiotensin-converting enzyme…”
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  12. 12

    Glutathione s-transferase m1 and t1 gene polymorphisms are not associated with increased risk of gestational diabetes mellitus development by Orhan, O, Atalay, M A, Orhan, F, Karkucak, M, Centinkaya Demir, B, Yakut, T, Cengiz, C

    Published in West Indian medical journal (01-08-2014)
    “…The aim of this study was to investigate whether the glutathione S-transferase M1 (GSTM1) and T1 (GSTT1) gene polymorphisms contributed to development of…”
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  13. 13

    Cathecol-O-methyl transferase Val158Met genotype is not a risk factor for conversion disorder by Armagan, E, Almacıoglu, M L, Yakut, T, Köse, A, Karkucak, M, Köksal, O, Görükmez, O

    Published in Genetics and molecular research (19-03-2013)
    “…Alterations in catechol-O-methyltransferase (COMT) activity are involved in various types of neurological disorders. We examined a possible association between…”
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  14. 14

    Subtelomeric fish findings in Turkish patients with idiopathic mental retardation by Tos, T, Vurucu, S, Karkucak, M, Kozan, S, Gul, D, Akin, R

    Published in Genetic counseling (01-01-2013)
    “…Subtelomeric rearrangements are the major cause of idiopathic mental retardation (IMR). This study included 67 Turkish children with IMR. Subtelomere…”
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    Investigation of ABCB1 gene polymorphism with colchicine response in Behçet's disease by Saricaoglu, H, Yilmaz, M, Karkucak, M, Ozturk, H Z Y, Yakut, T, Gulten, T, Baskan, E B, Aydogan, K, Dilek, K

    Published in Genetics and molecular research (01-01-2011)
    “…Colchicine is commonly used in the treatment of Behçet's disease. However, some patients are unresponsive to colchicine treatment. Adenosine…”
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  17. 17

    The variant translocation of ABL1 gene t(2;9)(q21;q34) in a childhood T-cell acute lymphoblastic leukemia by Karkucak, M, Yakut, T, Baytan, B, Gulten, T, Gunes, A M

    Published in Bratislavské lékarské listy (2012)
    “…We present the case of the childhood ALL that was identified by the translocation of the ABL1 gene to the q21 band of chromosome 2 without t(9;22)(q34;q11)…”
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  18. 18

    Performance of simple calculated osteoporosis risk estimation in a sample of women with suspected osteoporosis in the turkish population by Karkucak, M., Capkin, E., Kerimoglu, S., Serdaroglu, M., Topbas, M., Yildiz, H., Guler, M.

    Published in Rheumatology international (01-07-2008)
    “…The aim of this study was to evaluate the performance of the simple calculated osteoporosis risk estimation (SCORE) in a random sample of postmenopausal women…”
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  19. 19

    Toll-like receptor 9 polymorphism in patients with erythema multiforme, Stevens Johnson syndrome and Stevens Johnson syndrome/toxic epidermal necrolysis overlap syndrome by Turan, H, Bulbul Baskan, E, Yakut, T, Karkucak, M, Tunali, S, Saricaoglu, H

    Published in Bratislavské lékarské listy (2011)
    “…"Toll like receptor" (TLR) 9 functions in stepping in of native immune system against different viral and bacterial pathogens and induction of adaptive immune…”
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  20. 20

    Age-related diseases; degenerative aortic valve disease and osteoarthritis by Karkucak, M, Kiris, A, Capkin, E, Durmus, I, Ozden, G, Cansu, A, Tosun, M

    Published in Bratislavské lékarské listy (2010)
    “…To examine the relationship between degenerative aortic valve disease and osteoarthritis Background: Degenerative aortic valve disease (DAVD) and…”
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