Search Results - "Telatar, M."

Blood coagulation and fibrinolysis in patients with hyperthyroidism by EREM, C, ERSOZ, H. Ö, KARTI, S. S, UKINC, K, HACIHASANOGLU, A, DEGER, O, TELATAR, M

“…Several papers concerning abnormalities of blood coagulation and fibrinolysis during hyperthyroidism, have been published. Increased von Willebrand Factor…”
Get full text

Ataxia-Telangiectasia : Mutations in ATM cDNA detected by protein-truncation screening by TELATAR, M, WANG, Z, UDAR, N, LIANG, T, BERNATOWSKA-MATUSZKIEWICZ, E, LAVIN, M, SHILOH, Y, CONCANNON, P, GOOD, R. A, GATTI, R. A

“…We have examined the distal half of the ataxia-telangiectasia (A-T) gene transcript for truncation mutations in 48 A-T affecteds. We found 21 mutations; 4 of…”
Get full text

Effect of low-dose metoprolol in combination with sibutramine therapy in normotensive obese patients: a randomized controlled study by ERSOZ, H. O, UKINC, K, BAYKAN, M, EREM, C, DURMUS, I, HACIHASANOGLU, A, TELATAR, M

“…Sibutramine is an effective appetite suppresser agent, but treatment is often complicated with side effects, including palpitations and hypertension. In this…”
Get full text

Sphenoid sinus brown tumor, a mass lesion of occipital bone and hypercalcemia: an unusual presentation of primary hyperparathyroidism by Erem, C, Hacihasanoglu, A, Cinel, A, Ersöz, H Onder, Reis, A, Sari, A, Köse, M, Ukinç, K, Telatar, M

“…Brown tumor is a focal lesion of the bone caused by primary or, less commonly, secondary or tertiary hyperparathyroidism (HPT). While the mandible is the most…”
Get full text

New mutations, polymorphisms, and rare variants in the ATM gene detected by a novel SSCP strategy by Castellví-Bel, S., Sheikhavandi, S., Telatar, M., Tai, L-Q., Hwang, M., Wang, Z., Yang, Z., Cheng, R., Gatti, R.A.

“…The gene for ataxia‐telangiectasia, ATM, spans about 150 kb of genomic DNA. ATM mutations are found along the entire gene, with no evidence of a mutational hot…”
Get full text

Absence of mutations in the ATM gene in forty-seven cases of sporadic breast cancer by BEBB, D. G, YU, Z, CHEN, J, TELATAR, M, GELMON, K, PHILLIPS, N, GATTI, R. A, GLICKMAN, B. W

“…Epidemiological evidence points to an increased risk of breast cancer in ataxia telangiectasia (AT) heterozygote women. Previous attempts to screen early onset…”
Get full text

A Model for ATM Heterozygote Identification in a Large Population: Four Founder-Effect ATM Mutations Identify Most of Costa Rican Patients with Ataxia Telangiectasia by Telatar, M., Wang, Z., Castellvi-Bel, S., Tai, L-Q., Sheikhavandi, S., Regueiro, J.R., Porras, O., Gatti, R.A.

“…Ataxia telangiectasia (A-T) is an autosomal recessive disorder with a broad range of clinical manifestations and a frequency of 1:40,000–100,000 live births…”
Get full text

Dinucleotide repeat polymorphism at the NCAM locus by Telatar, M, Concannon, P, Tolun, A

Get more information

Thyroid function tests in pregnant women with and without goiter in the eastern Black Sea region by EREM, C, KAVGACI, H, KARAHAN, C, MOCAN, M. Z, TELATAR, M

“…Maternal thyroid function was investigated in 29 pregnant women with goiter and 51 pregnant women without goiter in the eastern Black Sea region of Turkey,…”
Get full text

Prevalence of obesity and associated risk factors in a Turkish population (Trabzon City, Turkey) by Erem, C, Arslan, C, Hacihasanoglu, A, Deger, O, Topbas, M, Ukinc, K, Ersoz, H.O, Telatar, M

“…Objective: To estimate the prevalence of overweight and obesity (general and central) in the Trabzon Region and its associations with demographic factors (age,…”
Get full text

Myocardial Perfusion Scintigraphy in a Myocardial Bridging of Coronary Artery by KULAN, KAAN, KULAN, CANSEL, TUNCER, CEMAL, KOMSUOĞLU, BAKI, TELATAR, MÜNIR

“…In myocardial bridging, muscle bonds may cause extreme narrowing of a coronary artery during systole. The case of a 17-year-old boy with coronary bridging in…”
Get full text

Relationships among nonverbal intelligence, hand speed, and serum testosterone level in left-handed male subjects by Tan, U, Akgün, A, Telatar, M

“…The relationships among nonverbal intelligence, hand speed, and serum testosterone level were studied in male left-handers ranging in age from 17 to 19 years…”
Get more information

New localization of NCAM, proximal to DRD2 at chromosome 11q23 by Telatar, M, Lange, E, Uhrhammer, N, Gatti, R A

Get full text

Cystic fibrosis patients from the Black Sea region: the 1677delTA mutation by Angelicheva, D, Boteva, K, Jordanova, A, Savov, A, Kufardjieva, A, Tolun, A, Telatar, M, Akarsubaşi, A, Köprübaşi, F, Aydoğdu, S

“…A 2 bp deletion in exon 10 of the CFTR gene, 1677delTA, which is very rare among CF chromosomes worldwide, was found to be a relatively common cause of cystic…”
Get more information

Urinary beta 2-microglobulin levels and urinary N-acetyl-beta-D-glucosaminidase enzyme activities in early diagnosis of non-insulin-dependent diabetes mellitus nephropathy by Mocan, Z, Erem, C, Yildirim, M, Telatar, M, Değer, O

“…To assess whether urinary N-acetyl-beta-D-glucosaminidase (NAG) and beta 2-microglobulin (beta 2-MG) levels could be used as predictors of diabetic nephropathy…”
Get more information

Splicing Defects in the Ataxia-Telangiectasia Gene, ATM: Underlying Mutations and Consequences by Teraoka, Sharon N., Telatar, Milhan, Becker-Catania, Sara, Liang, Teresa, Önengüt, Suna, Tolun, Asli, Chessa, Luciana, Sanal, Özden, Bernatowska, Eva, Gatti, Richard A., Concannon, Patrick

“…Mutations resulting in defective splicing constitute a significant proportion (30/62 [48%]) of a new series of mutations in the ATM gene in patients with…”
Get full text

Infant hearing loss and connexin testing in a diverse population by Schimmenti, Lisa A., Martinez, Ariadna, Telatar, Milhan, Lai, Chih-Hung, Shapiro, Nina, Fox, Michelle, Warman, Berta, McCarra, Matthew, Crandall, Barbara, Sininger, Yvonne, Grody, Wayne W., Palmer, Christina G.S.

“…Previous studies of connexin-related hearing loss have typically reported on mixed age groups or adults. To further address epidemiology and natural history of…”
Get full text

Coagulation and Fibrinolysis Parameters in Type 2 Diabetic Patients with and without Diabetic Vascular Complications by Erem, Cihangir, Hacıhasanoğlu, Arif, Çelik, Şükrü, Ovalı, Ercüment, Ersöz, H. Önder, Ukinç, Kubilay, Deger, Orhan, Telatar, Münir

“…Objectives: To investigate the markers of endogenous coagulation/fibrinolysis and vascular endothelial cell function, and to assess the relationships between…”
Get full text

Screening for Gestational Diabetes Mellitus in Northeastern Turkey (Trabzon City) by Erem, Cihangir, Cihanyurdu, Nihat, Deger, Orhan, Karahan, Caner, Çan, Gamze, Telatar, Münir

“…Objective: The purposes of this study were to determine the prevalence of gestational diabetes mellitus (GDM) in Trabzon city of Turkey and to identify…”
Get full text

Ataxia-Telangiectasia: Identification and Detection of Founder-Effect Mutations in the ATM Gene in Ethnic Populations by Telatar, Milhan, Teraoka, Sharon, Wang, Zhijun, Chun, Helen H., Liang, Teresa, Castellvi-Bel, Sergi, Udar, Nitin, Borresen-Dale, Anne-Lise, Chessa, Luciana, Bernatowska-Matuszkiewicz, Eva, Porras, Oscar, Watanabe, Mitsunori, Junker, Anne, Concannon, Patrick, Gatti, Richard A.

“…To facilitate the evaluation of ATM heterozygotes for susceptibility to other diseases, such as breast cancer, we have attempted to define the most common…”
Get full text