Search Results - "Baris, S."

Comprehensive comparison between 222 CTLA‐4 haploinsufficiency and 212 LRBA deficiency patients: a systematic review by Jamee, M., Hosseinzadeh, S., Sharifinejad, N., Zaki‐Dizaji, M., Matloubi, M., Hasani, M., Baris, S., Alsabbagh, M., Lo, B., Azizi, G.

“…Summary Cytotoxic T lymphocyte antigen 4 (CTLA‐4) haploinsufficiency (CHAI) and lipopolysaccharide‐responsive beige‐like anchor (LRBA) deficiency (LATAIE) are…”
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Over-specified referring expressions impair comprehension: An ERP study by Engelhardt, Paul E., Barış Demiral, Ş., Ferreira, Fernanda

“…► We examined whether comprehension is impaired with too much information. ► RTs and ERPs revealed that an extra modifier slowed comprehension and produced an…”
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Vitamin D as an adjunct to subcutaneous allergen immunotherapy in asthmatic children sensitized to house dust mite by Baris, S., Kiykim, A., Ozen, A., Tulunay, A., Karakoc‐Aydiner, E., Barlan, I. B.

“…Background We aimed to investigate the efficacy, safety, and T regulatory cell response of vitamin D as an adjunct to allergen‐specific immunotherapy (IT)…”
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Artificial Intelligence in Breast Imaging: Opportunities, Challenges, and Legal-Ethical Considerations by Subasi, Irmak Durur, Özçelik, Ş Barış

“…This review explores the transformative impact of artificial intelligence (AI) in breast imaging, driven by a global rise in breast cancer cases. Propelled by…”
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The use of the CT90 value in predicting anxiety in OSA: could it be a useful parameter? by Alkilinc, E, Ilgazli, A H, Boyaci, H, Basyigit, I, Argun Baris, S, Ozgun, S

“…Obstructive sleep apnea (OSA) is characterized by recurrent episodes of complete or partial obstruction of the upper airway leading to episodic desaturation…”
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Long-Term Effect of Sublingual and Subcutaneous Immunotherapy in Dust Mite-Allergic Children With Asthma/Rhinitis: A 3-Year Prospective Randomized Controlled Trial by Karakoc-Aydiner, E, Eifan, A O, Baris, S, Gunay, E, Akturk, E, Akkoc, T, Bahceciler, N N, Barlan, I B

“…Specific allergen immunotherapy is the only treatment modality that might change the natural course of allergic diseases in childhood. We sought to…”
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JAGN1 Deficient Severe Congenital Neutropenia: Two Cases from the Same Family by Baris, S., Karakoc–Aydiner, E., Ozen, A., Delil, K., Kiykim, A., Ogulur, I., Baris, I., Barlan, I. B.

“…Recently autosomal recessively inherited mutations in the gene encoding Jagunal homolog 1 (JAGN1) was described as a novel disease-causing gene of severe…”
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Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2 by van den Boogaard, M.L., Thijssen, P.E., Aytekin, C., Licciardi, F., Kıykım, A.A., Spossito, L., Dalm, V.A.S.H., Driessen, G.J., Kersseboom, R., de Vries, F., van Ostaijen‐ten Dam, M.M., Ikinciogullari, A., Dogu, F., Oleastro, M., Bailardo, E., Daxinger, L., Nain, E., Baris, S., van Tol, M.J.D., Weemaes, C., van der Maarel, S.M.

“…Background Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome is a rare, genetically heterogeneous, autosomal recessive disorder…”
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Development and validation of a cost-effective in-house method, tetra-primer ARMS PCR assay, in genotyping of seven clinically important point mutations by Etlik, Ozdal, Koksal, Vedat, Arican-Baris, S. Tugba, Baris, Ibrahim

“…The single nucleotide polymorphism (SNP) genotyping is currently considered as a particularly valuable tool for the diagnosis of different pathologies. For…”
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Seismotectonics of the Armutlu peninsula (Marmara Sea, NW Turkey) from geological field observation and regional moment tensor inversion by Kinscher, J., Krüger, F., Woith, H., Lühr, B.G., Hintersberger, E., Irmak, T.S., Baris, S.

“…The Armutlu peninsula, located in the eastern Marmara Sea, coincides with the western end of the rupture of the 17 August 1999, İzmit MW 7.6 earthquake which…”
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Spectral determination of source parameters in the Marmara Region by Koseolu, A, Oezel, N M, Baris, S, Uecer, S B, Ottemoller, L

“…Ever since the 1999 Kocaeli earthquake, in which the Kandilli Observatory and Earthquake Research Institute (KOERI) was not able to correctly reflect the…”
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A robust and efficient model for transmission of surface plasmon polaritons onto metal–insulator–metal apertures by Barış İplikçioğlu, S, Aksun, M I

“…Abstract A simple yet accurate model for the transmission of surface plasmon polaritons (SPPs) in a finite metal–insulator–metal (MIM) waveguide to the sides…”
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Angiotensin-converting enzyme insertion/deletion polymorphism has no effect on the risk of atherosclerotic stroke or hypertension by Tascilar, N, Dursun, A, Ankarali, H, Mungan, G, Ekem, S, Baris, S

“…Abstract Background and purpose Stroke is a heterogeneous multifactorial disease. Hence, a large number of candidate genes are involved in stroke…”
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Superior ovarian nerve (SON) transection leads to stunted follicular maturation: a histomorphologic and morphometric analysis in the rat model by Doganay, Melike, M.D, Simsek, Adnan, M.D, Tapisiz, Omer L., M.D, Mulazimoglu, Baris S., D.V.M., Ph.D, Yumusak, Nihat, Vet.Med, Gungor, Tayfun, Asst.Prof

“…Histomorphologic and morphometric effects of peripubertal superior ovarian nerve (SON) transection were evaluated during adult life in rats. Twenty…”
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Comparing tissue coring potentials of hollow needles without stylet and caudal needles with stylet: an experimental study by Guldogus, F., Baris, Y. S., Baris, S., Karakaya, D., Kelsaka, E.

“…BACKGROUND AND OBJECTIVESAlthough the association of tissue coring and development of epidermoid tumour has been proposed, the extent and frequency of such…”
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Papaverine chloride as a topical vasodilator in accidental injection of adrenaline into a digital finger by Baris, S., Saricoban, H. E., Ak, K., Ozdemir, C.

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Rapid diagnosis of spinal muscular atrophy using tetra-primer ARMS PCR assay: Simultaneous detection of SMN1 and SMN2 deletion by Baris, Ibrahim, Etlik, Ozdal, Koksal, Vedat, Arican-Baris, S. Tugba

“…Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive…”
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Alteration in humoral immunity is common among family members of patients with common variable immunodeficiency by Karakoc-Aydiner, E, Ozen, A O, Baris, S, Ercan, H, Ozdemir, C, Barlan, I B

“…The prevalence of primary immunodeficiency (PID) in the relatives of patients with common variable immunodeficiency (CVID) and IgA deficiency is high. Allergic…”
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Predictors of atopic dermatitis phenotypes and severity: roles of serum immunoglobulins and filaggrin gene mutation R501X by Ercan, H, Ispir, T, Kirac, D, Baris, S, Ozen, A, Oztezcan, S, Cengizlier, M R

“…Atopic dermatitis (AD), the most common chronic relapsing skin condition of infancy and childhood, is a complex multifactorial disease, which arises from the…”
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Efficacy of intravenous immunoglobulin treatment in children with common variable immunodeficiency by Baris, S, Ercan, H, Cagan, H Hasret, Ozen, A, Karakoc-Aydiner, E, Ozdemir, C, Bahceciler, N N

“…Children with common variable immunodeficiency (CVID) have increased susceptibility to infections. We evaluated the role of intravenous immunoglobulin (IVIG)…”
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