Search Results - "ARTAC, H."

Evaluation of T-cell subsets in pregnant women infected with SARS-CoV-2 by Kulhan, M., Ozdemir, H., Bilgi, A., Celik, C., Aktug Demir, N., Turk Dagi, H., Ucar, M.G., Kulhan, N.G., Artac, H.

“…•The CD3+ total T cell ( p = 0.001), CD3+CD4+ helper T cell ( p = 0.011), Treg ( p = 0.001), and Treg/Th17 ratio ( p = 0.001) were found to be lower in…”
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CD3G Gene Defects in Familial Autoimmune Thyroiditis by Gokturk, B., Keles, S., Kirac, M., Artac, H., Tokgoz, H., Guner, S. N., Caliskan, U., Caliskaner, Z., Burg, M., Dongen, J., Morgan, N. V., Reisli, I.

“…The patients with CD3γ deficiency can present with different clinical findings despite having the same homozygous mutation. We report three new…”
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B-cell maturation and antibody responses in individuals carrying a mutated CD19 allele by Artac, H, Reisli, I, Kara, R, Pico-Knijnenburg, I, Adin-Çinar, S, Pekcan, S, Jol-van der Zijde, C M, van Tol, M J D, Bakker-Jonges, L E, van Dongen, J J M, van der Burg, M, van Zelm, M C

“…Homozygous CD19 mutations lead to an antibody deficiency due to disruption of the CD19 complex and consequent impaired signaling by the B-cell antigen…”
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Type III bare lymphocyte syndrome associated with a novel RFXAP mutation: a case report by Gokturk, B., Artac, H., van Eggermond, M. J., van den Elsen, P., Reisli, İ.

“…Summary Type III bare lymphocyte syndrome (BLS) is a severe combined immunodeficiency disease caused by the absence of MHC Class II expression associated with…”
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Vernal keratoconjunctivitis—A rare but serious comorbidity of allergic rhinitis and eustachian tube dysfunction by Bozkurt, M.K, Bozkurt, B, Artac, H, Arslan, N, Reisli, I

“…Abstract Objective To determine the prevalence of symptoms and signs of allergic rhinitis (AR) in children with vernal keratoconjunctivitis (VKC) and evaluate…”
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The Utility of Childhood Asthma Control Test and its Relationship with Control Measures and with the Decisions Made by Asthma Specialist by Sekerel, B.E, Keskin, O, Uzuner, N, Yazicioglu, M, Kilic, M, Artac, H, Ozmen, S, Can, D, Zeyrek, D, Cokugras, H, Soyer, O, Sapan, N, Aydogan, M, Kuyucu, S, Inal, A, Gurkan, F, Orhan, F, Yilmaz, O, Bingol Boz, A, Tahan, F, Cevit, O

“…Considering that suboptimal controlled disease is frequent, step-up asthma treatment level in uncontrolled patients may provide expected level of control and…”
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Esophageal cyst applied with asthma clinic by Pekcan, S, Aslan, E, Keles, S, Artac, H, Reisli, I, Odev, K, Arıbas, O

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Transferrin receptor in proliferation of T lymphocytes in infants with iron deficiency by ARTAC, H., COSKUN, M., KARADOGAN, I., YEGIN, O., YESILIPEK, A.

“…Summary The aim of this study was to contribute to clarify the mechanism of cellular immune insufficiency occurring during iron deficiency. We studied the…”
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The reliability and validity of Turkish version of Childhood Asthma Control Test by Sekerel, B. E., Soyer, O. U., Keskin, O., Uzuner, N., Yazicioglu, M., Kılıç, M., Artaç, H., Ozmen, S., Can, D., Zeyrek, D., Cokugras, H., Canitez, Y., Aydogan, M., Kuyucu, S., İnal, A., Gurkan, F., Orhan, F., Yilmaz, O., Boz, A. B., Tahan, F., Cevit, O.

“…Introduction The reliability and validity of Turkish version of Childhood Asthma Control Test (C-ACT). Purpose The management of asthma is an important as well…”
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Down syndrome associated with severe combined immunodeficiency: a case report by Yildirim, M S, Artac, H, Reisli, I

“…An 8-month-old boy was admitted to the hospital because of recurrent bronchopneumonia and gastrointestinal tract infections. On physical examination, he had…”
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A CASE WITH 18q DELETION SYNDROME IDENTIFIED WITH B CELL ABSENCE AND CONGENITAL HEART DISEASE by Güvenç, O, Çimen, D, Kaplan, M B, Aslan, E, Artaç, H, Annagür, A

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Approach to genetic diagnosis of inborn errors of immunity through next-generation sequencing by Karimi, Esmat, Mahmoudian, Fatemeh, Reyes, Saul O. Lugo, Bargir, Umair Ahmed, Madkaikar, Manisha, Artac, Hasibe, Sabzevari, Araz, Lu, Na, Azizi, Gholamreza, Abolhassani, Hassan

“…•Inborn errors of immunity (IEI) constitute a heterogeneous group of mainly monogenic primary immune disorders.•The human gene connectome analysis shows that…”
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The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity by Baris, Safa, Abolhassani, Hassan, Massaad, Michel J., Al-Nesf, Maryam, Chavoshzadeh, Zahra, Keles, Sevgi, Reisli, Ismail, Tahiat, Azzeddine, Shendi, Hiba Mohammad, Elaziz, Dalia Abd, Belaid, Brahim, Al Dhaheri, Fatima, Haskologlu, Sule, Dogu, Figen, Ben-Mustapha, Imen, Sobh, Ali, Galal, Nermeen, Meshaal, Safa, Elhawary, Rabab, El-marsafy, Aisha, Alroqi, Fayhan J., Al-Saud, Bandar, Al-Ahmad, Mona, Al Farsi, Tariq, AL Sukaiti, Nashat, Al-Tamemi, Salem, Mehawej, Cybel, Dbaibo, Ghassan, ElGhazali, Gehad, Kilic, Sara Sebnem, Genel, Ferah, Kiykim, Ayca, Musabak, Ugur, Artac, Hasibe, Guner, Sukru Nail, Boukari, Rachida, Djidjik, Reda, Kechout, Nadia, Cagdas, Deniz, El-Sayed, Zeinab Awad, Karakoc-Aydiner, Elif, Alzyoud, Raed, Barbouche, Mohamed Ridha, Adeli, Mehdi, Wakim, Rima Hanna, Reda, Shereen M., Ikinciogullari, Aydan, Ozen, Ahmet, Bousfiha, Aziz, Al-Mousa, Hamoud, Rezaei, Nima, Al-Herz, Waleed, Geha, Raif S.

“…Human inborn errors of immunity (IEI) are a group of 485 distinct genetic disorders affecting children and adults. Signs and symptoms of IEI are heterogeneous,…”
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Systemic Atopy and Immunoglobulin Deficiency in Turkish Patients with Vernal Keratoconjunctivitis by Bozkurt, Banu, Artac, Hasibe, Arslan, Nasha, Gokturk, Bahar, Bozkurt, Mete Kaan, Reisli, Ismail, Irkec, Murat

“…Purpose: To determine the prevalence of systemic atopy and immunoglobulin (Ig) deficiencies in vernal keratoconjunctivitis (VKC). Methods: Sixty-seven VKC…”
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Chilaiditi syndrome as a cause of respiratory distress by KELES, Sevgi, ARTAC, Hasibe, REISLI, Ismail, ALP, Hayrullah, KOC, Osman

“…Chilaiditi syndrome is the interposition of the colon between the diaphragma and the liver. In general, patients are asymptomatic, but some patients have been…”
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Late-presenting congenital diaphragmatic hernia associated with ectopic thoracic kidney by KELES, Sevgi, ARTAC, Hasibe, ELMACI, Midhat, REISLI, Ismail, DILSIZ, Alaaddin

“…Although congenital defects of diaphragma often occur in the period immediately following birth, 10-20% of these cases are diagnosed later. We report on a…”
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