Search Results - "İmirzalıoğlu, N."

Relationship between granular cytoplasm of oocytes and pregnancy outcome following intracytoplasmic sperm injection by Kahraman, S., Yakın, K., Dönmez, E., Şamlı, H., Bahçe, M., Cengiz, G., Sertyel, S., Şamlı, M., İmirzalıoğlu, N.

“…Couples undergoing intracytoplasmic sperm injection (ICSI) for male infertility using oocytes with centrally located granular cytoplasm (CLCG) were evaluated…”
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Healthy births and ongoing pregnancies obtained by preimplantation genetic diagnosis in patients with advanced maternal age and recurrent implantation failure by Kahraman, S., Bahçe, M., Şamlı, H., İmirzalıoğlu, N., Yakısn, K., Cengiz, G., Dönmez, E.

“…Preimplantation genetic diagnosis (PGD) and subsequent embryo development was evaluated in 72 couples presenting at our centre for intracytoplasmic sperm…”
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IL-15 Gene Polymorphism Associated With Early Marginal Bone Loss Around Endosseous Dental Implants by Suer, B.T, Kocyigit, I.D, Atil, F, Suer, F.E, Keceli, G, Tekin, U, Imirzalioglu, N

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MEFV gene is a probable susceptibility gene for Behçet's disease by Im rzal oglu, N., Dursun, A., Tastan, B., Soysal, Y., Yak c er, M. C.

“…Objective: Behçet's disease (BD) is a rare, chronic, multisystem inflammatory disorder. The prevalence of BD is higher in the Middle Eastern and Mediterranean…”
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Molecular characterization of microduplication 22q11.2 in a girl with hypernasal speech by Soysal, Y, Vermeesch, J, Davani, N A, Şensoy, N, Hekimler, K, İmirzalıoğlu, N

“…We present a 12-year-old girl with karyotype 46,XX. A comparative genomic hybridization array revealed a 3.172-Mb microduplication on 22q11.2. This chromosome…”
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A patient with ascending aortic dilatation, similar to phenotypes of connective tissue disorders by Onrat, S T, Emmiler, M, Sivaci, Y, Söylemez, Z, Ozgöz, A, Imirzalioğlu, N

“…We report on the clinical and molecular findings of a patient who presented alopecia, epicanthus, micrognathia, retrognathia, high arched palate,…”
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Effect of Helicobacter pylori infection and eradication therapy on interleukin-6 levels in patients with Familial Mediterranean Fever by Ozel, A M, Demirturk, L, Aydogdu, A, Gultepe, M, Yazgan, Y, Imirzalioglu, N, Gurbuz, A K, Narin, Y

“…It is being questioned if Helicobacter pylori infection, which causes a chronic inflammatory response, can increase the frequency and severity of attacks in…”
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GENETIC ANOMALIES DETECTED IN PATIENTS WITH NON-OBSTRUCTIVE AZOOSPERMIA AND OLIGOZOOSPERMIA by Samli, H., Samli, M. M., Solak, M., Imirzalioglu, N.

“…Genetic factors have a major importance in male infertility etiology. Numerical and structural chromosomal abnormalities seem to be frequent inoligospermia and…”
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Clinical and intraoral findings of a patient with tricho-rhino-phalangeal syndrome type I by Karacay, S, Saygun, I, Tunca, Y, Imirzalioglu, N, Guvenc, G

“…Tricho-rhino-phalangeal syndrome (TRPS) is a rare and an autosomal dominant disorder having the following characteristics: slowly growing sparse hair, medially…”
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Familial secundum type atrial septal defect with normal karyotypes by Buyukates, M, Turan, S A, Altunkaya, S A, Imirzalioglu, N

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The vitamin D receptor fokl start codon polymorphism and bone mineral density in male hypogonadotrophic hypogonadism by Bolu, S. E., Orkunoglu Suer, F. E., Deniz, F., Ückaya, G., Imirzalioglu, N., Kutlu, M.

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Prenatal diagnosis of autosomal recessive osteopetrosis, infantile type, by X-ray evaluation by Oğur, G, Oğur, E, Celasun, B, Baser, I, Imïrzalioğlu, N, Oztürk, T, Alemdaroğlu, A

“…Prenatal diagnosis for infantile osteopetrosis was attempted during the third pregnancy of a first-cousin marriage whose family history revealed an affected…”
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The effects of folic acid application on IL-1beta levels of human gingival fibroblasts stimulated by phenytoin and TNFalpha in vitro: a preliminary study by Doğan, A, Tunca, Y, Ozdemir, A, Sengül, A, Imirzalioğlu, N

“…Folic acid (FA), that is required for the integrity of gingival tissues, was found to decrease in patients using phenytoin (PHT). Interleukin-1 beta (IL-1beta)…”
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Application of the 'Apt test' in Prenatal Diagnosis to evaluate the Fetal Origin of Blood obtained by Cordocentesis: results of 30 pregnancies by Ogur, G., Gül, D., Özen, S., Imirzalioglu, N., Cankus, G., Tunca, Y., Bahçe, M., Güran, S., Baser, I.

“…This study aimed to set up a practical lab‐side approach to discriminate fetal from maternal blood in samples obtained by cordocentesis. To determine the fetal…”
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CLINICAL, ANDROLOGICAL AND GENETIC CHARACTERISTICS OF PATIENTS WITH CONGENITAL BILATERAL ABSENCE OF VAS DEFERENS (CBAVD) by Samli, H., Samli, M. M., Yilmaz, E., Imirzalioglu, N.

“…Congenital bilateral absence of the vas deferens (CBAVD) is a form of infertility with an autosomal recessive genetic background in otherwise healthy males. In…”
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Age-related macular degeneration and association of CFH Y402H and LOC387715 A69S polymorphisms in a Turkish population by Soysal, Yasemin, Inan, Umit Übeyt, Küsbeci, Tuncay, Imirzalioğlu, Necat

“…Age-related macular degeneration (AMD) is a disease with multifactorial etiology characterized by irreversible loss of central visual acuity. The discovery of…”
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Variable clinical expression of Holt-Oram syndrome in three generations by Oğur, G, Gül, D, Lenk, M K, Imirzalioğlu, N, Alpay, F, Oğur, E

“…Holt-Oram syndrome is a distinct autosomal dominant entity presenting with upper limb defects and cardiac abnormality. No correlation between the severity of…”
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Modulator effects of the methylenetetrahydrofolate reductase C677T polymorphism on response to vitamin B12 therapy and homocysteine metabolism by Sensoy, Nazli, Şoysal, Yasemin, Kahraman, Ahmet, Doğan, Nurhan, Imirzalioğlu, Necat

“…In this study, our aim was to investigate the association of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism on the vitamin B12 therapy response…”
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Case Report Molecular characterization of microduplication 22q11.2 in a girl with hypernasal speech by Soysal, Y., Vermeesch, J., Davani, N.A., Şensoy, N., Hekimler, K., Imirzalıoğlu, N.

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Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy by Soysal, Yasemin, Balcı, Sevim, Hekimler, Kuyaş, Liehr, Thomas, Ewers, Elisabeth, Schoumans, Jacqueline, Bui, The‐Hung, İçduygu, Fadime Mutlu, Kosyakova, Nadezda, İmirzalıoğlu, Necat

“…We present the clinical and molecular findings in a Turkish child with a de novo mosaic ring derived from chromosome 4 with multiple cell‐lines; the karyotype…”
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