Search Results - "Karkucak, M"
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Assessment of hand function and disability in fibromyalgia
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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2
Sexual function in male patients with ankylosing spondylitis
Published in International journal of impotence research (01-11-2011)“…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
SRY-negative XX sex reversal in an English Cocker Spaniel: a case report
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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The prevalence and risk factors of low back pain in the eastern Black Sea region of Turkey
Published in Journal of back and musculoskeletal rehabilitation (01-01-2015)“…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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A RARE COMBINATION OF 45,X/46,XY MOSAICISM AND Y CHROMOSOME MICRODELETION IN AN INFERTILE MAN WITH AZOOSPERMIA
Published in Genetic counseling (2016)Get more information
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6
Polymorphisms of glutathione-s-transferase M1, T1, and P1 genes in endometrial carcinoma
Published in European journal of gynaecological oncology (2013)“…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
Polymorphisms in angiotensin-converting enzyme and glutathione s-transferase genes in Turkish population and risk for preeclampsia
Published in Clinical and experimental obstetrics & gynecology (2012)“…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
Ultrasonographic evaluation of femoral cartilage thickness in patients with ankylosing spondylitis
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
Lack of association of ACE gene I/D polymorphism with obstructive sleep apnea syndrome in Turkish patients
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
Another small supernumerary marker chromosome derived from chromosome 9 in a Klinefelter patient
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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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
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
Glutathione s-transferase m1 and t1 gene polymorphisms are not associated with increased risk of gestational diabetes mellitus development
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
Cathecol-O-methyl transferase Val158Met genotype is not a risk factor for conversion disorder
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
Subtelomeric fish findings in Turkish patients with idiopathic mental retardation
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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15
Toll-like receptor-9 gene polymorphism in common variable immunodeficiency
Published in Journal of investigational allergology & clinical immunology (2010)Get full text
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16
Investigation of ABCB1 gene polymorphism with colchicine response in Behçet's disease
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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The variant translocation of ABL1 gene t(2;9)(q21;q34) in a childhood T-cell acute lymphoblastic leukemia
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
Performance of simple calculated osteoporosis risk estimation in a sample of women with suspected osteoporosis in the turkish population
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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Toll-like receptor 9 polymorphism in patients with erythema multiforme, Stevens Johnson syndrome and Stevens Johnson syndrome/toxic epidermal necrolysis overlap syndrome
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
Age-related diseases; degenerative aortic valve disease and osteoarthritis
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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