Search Results - "Yildiran, A"

A comparison of B cell subsets in primary immune deficiencies that progress with antibody deficiency and age-matched healthy children by Celiksoy, M H, Yildiran, A

“…The objective of this study was to examine the B lymphocyte subsets in primary immunodeficiency that progress with antibody deficiency. The patients' naive,…”
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The role of active B cells in allergen immunotherapy by Celiksoy, M H, Sancak, R, Yildiran, A

“…The purpose of this study is to examine the changes in B lymphocyte subsets in patients receiving allergen immunotherapy. B lymphocyte subsets of patients…”
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Is parturition-timing machinery related to the number of inhibitor CD94/NKG2A positive uterine natural killer cells? by Mazi, E., Altunkaynak, Z., Aydin, I., Kocak, I., Guven, D., Turkmen, A. P., Yildiran, A.

“…Purpose Prematurity is the most common cause of infant mortality and morbidity. To prevent this, the timing of parturition and its mechanisms should be…”
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Breath holding spells in 91 children and response to treatment with iron by Mocan, Hilal, Yildiran, Alisan, Orhan, Fazil, Erduran, Erol

“…To evaluate the prognosis of breath holding spells (BHS) after iron treatment, 91 children (56 boys, 35 girls) aged between 6 months and 40 months (median, 17)…”
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The role of basophil activation test in venom ımmunotherapy: comparative evaluation with specific IgE and skin prick tests, ınnovative approaches by Kokcu Karadag, S I, Özen Çökelez, S, Bekar Çepniler, E, Abdullayev, E, Terzi, O, Özçeker, D, Sancak, R, Yıldıran, A

“…In diagnosing insect venom allergy and making immunotherapy decisions, clinical history, skin tests, and specific serum IgE levels are commonly utilized. This…”
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HLA Class I Deficiency: Clinical, Immunological and Genetic Characteristics of Three Patient by Ikinciogullari, A, Dogu, F, Fricker, D, Yuksek, M, Bozdogan, G, Aytekin, C, Yildiran, A, Ciftci, E, Can, Z, Babacan, E, De La Salle, H

“…[...]case was 10 years-old boy who has persistant granulomatous skin lesions located on midface since last year…”
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An unusual clinical presentation: invasive Candida non-albicans infections in ataxia telangiectasia by Cipe, F, Dogu, F, Yildiran, A, Yüksek, M, Pekacar, T, Güriz, H, Saatci, M, Sezer, E, Düzenli, F, Ikinciogullari, A, Babacan, E

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Comparison of major lymphocyte subpopulations and recent thymic emigrants in patients with ataxia telangiectasia and age-matched healthy groups by Celiksoy, M H, Topal, E, Yıldıran, A

“…Ataxia telangiectasia (A-T) is a genetic disorder caused by the homozygous mutation of the A-T mutated gene. It is frequently associated with variable degrees…”
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Impaired respiratory burst contributes to infections in PKC-deficient patients by Neehus, A-L, Moriya, K, Nieto-Patlan, A, Le, Voyer T, Levy, R, Ozen, A, Karakoc-Aydiner, E, Baris, S, Yildiran, A, Altundag, E

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Impaired respiratory burst contributes to infections in PKCδ-deficient patients by Neehus, Anna-Lena, Moriya, Kunihiko, Nieto-Patlán, Alejandro, Le Voyer, Tom, Lévy, Romain, Özen, Ahmet, Karakoc-Aydiner, Elif, Baris, Safa, Yildiran, Alisan, Altundag, Engin, Roynard, Manon, Haake, Kathrin, Migaud, Mélanie, Dorgham, Karim, Gorochov, Guy, Abel, Laurent, Lachmann, Nico, Dogu, Figen, Haskologlu, Sule, İnce, Erdal, El-Benna, Jamel, Uzel, Gulbu, Kiykim, Ayca, Boztug, Kaan, Roderick, Marion R, Shahrooei, Mohammad, Brogan, Paul A, Abolhassani, Hassan, Hancioglu, Gonca, Parvaneh, Nima, Belot, Alexandre, Ikinciogullari, Aydan, Casanova, Jean-Laurent, Puel, Anne, Bustamante, Jacinta

“…Patients with autosomal recessive protein kinase C δ (PKCδ) deficiency suffer from childhood-onset autoimmunity, including systemic lupus erythematosus. They…”
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Novel NLRP12 mutations associated with intestinal amyloidosis in a patient diagnosed with common variable immunodeficiency by Borte, Stephan, Celiksoy, Mehmet Halil, Menzel, Volker, Ozkaya, Ozan, Ozen, Fatma Zeynep, Hammarström, Lennart, Yildiran, Alisan

“…Abstract Heterozygous mutations in the NLRP12 gene have been found in patients with systemic auto-inflammatory diseases. However, the NLRP12-associated…”
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Combined Immunodeficiencies: Clinical, Immunological Features And Outcome Of 56 Cases From A Single Institution by İkincioğullar, A, Doğu, F, Aytekin, C, Çipe, F.E, Yüksek, M, Bozdoğan, G, Yldran, A, Güloğlu, D, Babacan, E

“…Among SCID cases, T-B-NK+ (55%) is found to be the most common immunophenotype. 27 patients among 56 (19 SCID, 2 Omenn's Syndrome, 3 MHC Class II Deficiency, 1…”
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A case of VATER association associated with 9qh by Aynaci, F M, Celep, F, Karagüzel, A, Baki, A, Yildiran, A

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Impaired respiratory burst contributes to infections in PKCδ-deficient patients by Neehus, AL, Moriya, K, Patlan, AN, Le Voyer, T, Levy, R, Yildiran, A, Dogu, F, Haskologlu, S, Ince, E, Uzel, G, Kiykim, A, Boztug, K, Roderick, M, Brogan, P, Abolhassani, H, Hancioglu, G, Parvareh, N, Belot, A, Ikinciogullari, A, Casanova, JL, Puel, A, Bustamante, J

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Multiple vertebral segmentation defects. Brief report of three patients and nosological considerations by Aslan, Y, Erduran, E, Mocan, H, Yildiran, A, Okten, A, Gedik, Y

“…Multiple vertebral segmentation defects i.e. multiple malformations of vertebrae and ribs are characterized by short neck, scoliosis, short trunk and deformity…”
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Double-blind, placebo-controlled study of zinc sulfate in the treatment of attention deficit hyperactivity disorder by Bilici, Mustafa, Yıldırım, Fatma, Kandil, Sema, Bekaroğlu, Mehmet, Yıldırmış, Sermet, Değer, Orhan, Ülgen, Metin, Yıldıran, Alişan, Aksu, Hatice

“…Background: The most commonly used medications for attention deficit hyperactivity disorder (ADHD) are the psychostimulants. There is, however, considerable…”
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Autoimmune thyroiditis after haplo-identical stem cell transplantation for severe combined immunodeficiency by Dogu, F, Cipe, F, Yildiran, A, Siklar, Z, Yuksek, M, Ocal, G, Ikinciogullari, A

“…Introduction: Thyroid dysfunction is a well known complication in survivors of hematopoietic stem cell transplantation, and is reported after TBI as well as…”
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UNUSUAL CLINICAL PRESENTATION AND HEMOPHAGOCYTOSIS OF ATAXIA-TELANGIECTASIA IN TWO SIBLINGS WITH A RARE MUTATION by Yildiran, A, Celiksoy, MH, Guner, SN, Borte, S

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UNUSUAL CLINICAL PRESENTATION AND HEMOPHAGOCYTOSIS OF ATAXIA-TELANGIECTASIA IN TWO SIBLINGS WITH A RARE MUTATION by Yildiran, A, Celiksoy, MH, Guner, SN, Borte, S

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Pediatric hypereosinophilic syndrome (HES) clinically differs from adult HES, but there is a lack of confirmatory laboratory data by Yildiran, Alişan, İkincioğullari, Aydan

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