Takip et
Alisan Yildiran, MD
Alisan Yildiran, MD
omu.edu.tr üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery
EM Scott, A Halees, Y Itan, EG Spencer, Y He, MA Azab, SB Gabriel, ...
Nature genetics 48 (9), 1071-1076, 2016
3422016
Double-blind, placebo-controlled study of zinc sulfate in the treatment of attention deficit hyperactivity disorder
M Bilici, F Yıldırım, S Kandil, M Bekaroğlu, S Yıldırmış, O Değer, M Ülgen, ...
Progress in neuro-psychopharmacology and biological psychiatry 28 (1), 181-190, 2004
3152004
BCG vaccination in patients with severe combined immunodeficiency: complications, risks, and vaccination policies
BE Marciano, CY Huang, G Joshi, N Rezaei, BC Carvalho, Z Allwood, ...
Journal of allergy and clinical immunology 133 (4), 1134-1141, 2014
2702014
Inherited and acquired immunodeficiencies underlying tuberculosis in childhood
S Boisson‐Dupuis, J Bustamante, J El‐Baghdadi, Y Camcioglu, ...
Immunological reviews 264 (1), 103-120, 2015
2352015
Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients
MY Köker, Y Camcıoğlu, K Van Leeuwen, SŞ Kılıç, I Barlan, M Yılmaz, ...
Journal of allergy and clinical immunology 132 (5), 1156-1163. e5, 2013
2112013
TLR3 deficiency in herpes simplex encephalitis: high allelic heterogeneity and recurrence risk
HK Lim, M Seppänen, T Hautala, MJ Ciancanelli, Y Itan, FG Lafaille, ...
Neurology 83 (21), 1888-1897, 2014
1642014
Breath holding spells in 91 children and response to treatment with iron
H Mocan, A Yildiran, F Orhan, E Erduran
Archives of disease in childhood 81 (3), 261-262, 1999
1601999
Abatacept as a long-term targeted therapy for LRBA deficiency
A Kiykim, I Ogulur, E Dursun, LM Charbonnier, E Nain, S Cekic, ...
The Journal of Allergy and Clinical Immunology: In Practice 7 (8), 2790-2800 …, 2019
1342019
Bone mineral density in children with cerebral palsy
HA Tasdemir, M Buyukavci, F Akcay, P Polat, A Yildiran, C Karakelleoglu
Pediatrics International 43 (2), 157-160, 2001
762001
Could familial Mediterranean fever gene mutations be related to PFAPA syndrome?
MH Celiksoy, G Ogur, E Yaman, U Abur, S Fazla, R Sancak, A Yildiran
Pediatric Allergy and Immunology 27 (1), 78-82, 2016
442016
The role of high dose methylprednisolone and splenectomy in the accelerated phase of Chediak-Higashi syndrome
Y Aslan, E Erduran, Y Gedik, H Mocan, A Yildiran
Acta haematologica 96 (2), 105-107, 1996
351996
Novel NLRP12 mutations associated with intestinal amyloidosis in a patient diagnosed with common variable immunodeficiency
S Borte, MH Celiksoy, V Menzel, O Ozkaya, FZ Ozen, L Hammarström, ...
Clinical Immunology 154 (2), 105-111, 2014
322014
Apoptotic effects of heparin on lymphoblasts, neutrophils, and mononuclear cells: results of a preliminary in vitro study
E Erduran, Y Tekelioğlu, Y Gedik, A Yıldıran
American journal of hematology 61 (2), 90-93, 1999
321999
An unconditioned bone marrow transplantation in a child with purine nucleoside phosphorylase deficiency and its unique complication
C Aytekin, M Yuksek, F Dogu, A Yagmurlu, A Yildiran, S Fitoz, M Kologlu, ...
Pediatric transplantation 12 (4), 479-482, 2008
302008
Impaired respiratory burst contributes to infections in PKCδ-deficient patients
AL Neehus, K Moriya, A Nieto-Patlán, T Le Voyer, R Lévy, A Özen, ...
Journal of Experimental Medicine 218 (9), e20210501, 2021
292021
A case of VATER association associated with 9qh+.
FM Aynaci, F Celep, A Karagüzel, A Baki, A Yildiran
Genetic Counseling (Geneva, Switzerland) 7 (4), 321-322, 1996
291996
Successful treatment of reactive hemophagocytic syndrome with cyclosporin A and intravenous immunoglobulin.
E Erduran, Y Gedik, Y Sen, A Yildiran
The Turkish Journal of Pediatrics 42 (2), 168-170, 2000
272000
Clinical features and HSCT outcome for SCID in Turkey
A Ikinciogullari, D Cagdas, F Dogu, T Tugrul, G Karasu, S Haskologlu, ...
Journal of Clinical Immunology 39, 316-323, 2019
242019
Seven chronic granulomatous disease cases in a single-center experience and a review of the literature
S Kutlug, G Sensoy, A Birinci, B Saraymen, M Köker, A Yildiran
Asian Pacific journal of allergy and immunology 36 (1), 2018
242018
Transient tachypnea of the newborn (TTN): a role for polymorphisms of surfactant protein B (SP-B) encoding gene?
E Tutdibi, B Hospes, E Landmann, L Gortner, M Satar, M Yurdakök, ...
Klinische Pädiatrie 215 (05), 248-252, 2003
242003
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