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Türkan Patıroğlu
Türkan Patıroğlu
Verified email at erciyes.edu.tr - Homepage
Title
Cited by
Cited by
Year
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
3432016
Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels
A Sassi, S Lazaroski, G Wu, SM Haslam, M Fliegauf, F Mellouli, ...
Journal of allergy and clinical immunology 133 (5), 1410-1419. e13, 2014
2102014
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency
KR Engelhardt, ME Gertz, S Keles, AA Schäffer, EC Sigmund, C Glocker, ...
Journal of Allergy and Clinical Immunology 136 (2), 402-412, 2015
1952015
Hematologically important mutations: leukocyte adhesion deficiency (first update)
E Van De Vijver, A Maddalena, Ö Sanal, SM Holland, G Uzel, ...
Blood Cells, Molecules, and Diseases 48 (1), 53-61, 2012
1882012
Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency
R Lévy, S Okada, V Béziat, K Moriya, C Liu, LYA Chai, M Migaud, F Hauck, ...
Proceedings of the National Academy of Sciences 113 (51), E8277-E8285, 2016
1582016
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
1332019
Functional selectivity in cytokine signaling revealed through a pathogenic EPO mutation
AR Kim, JC Ulirsch, S Wilmes, E Unal, I Moraga, M Karakukcu, D Yuan, ...
Cell 168 (6), 1053-1064. e15, 2017
1112017
Inherited biallelic CSF3R mutations in severe congenital neutropenia
A Triot, PM Järvinen, JI Arostegui, D Murugan, N Kohistani, ...
Blood, The Journal of the American Society of Hematology 123 (24), 3811-3817, 2014
942014
Pancytopenia, a rare hematologic manifestation of brucellosis in children
M Karakukcu, T Patiroglu, MA Ozdemir, T Gunes, H Gumus, C Karakukcu
Journal of pediatric hematology/oncology 26 (12), 803-806, 2004
902004
Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease
JC Ravell, M Matsuda-Lennikov, SD Chauvin, J Zou, M Biancalana, ...
The Journal of clinical investigation 130 (1), 507-522, 2020
832020
Outcomes and treatment strategies for autoimmunity and hyperinflammation in patients with RAG deficiency
JR Farmer, Z Foldvari, B Ujhazi, SS De Ravin, K Chen, JJH Bleesing, ...
The Journal of Allergy and Clinical Immunology: In Practice 7 (6), 1970-1985. e4, 2019
692019
Late-type vitamin K deficiency bleeding: experience from 120 patients
MA Ozdemir, M Karakukcu, H Per, E Unal, H Gumus, T Patiroglu
Child's Nervous System 28, 247-251, 2012
602012
Nonacog beta pegol (N9-GP) in haemophilia B: a multinational phase III safety and efficacy extension trial (paradigm™ 4)
G Young, PW Collins, T Colberg, A Chuansumrit, H Hanabusa, SR Lentz, ...
Thrombosis research 141, 69-76, 2016
572016
Plasma soluble human leukocyte antigen G levels in asthmatic children
F Tahan, T Patıroglu
International archives of allergy and immunology 141 (3), 213-216, 2006
482006
Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis
B Tesi, K Lagerstedt-Robinson, SCC Chiang, EB Bdira, M Abboud, ...
Genome medicine 7, 1-13, 2015
472015
Rapamycin has a beneficial effect on controlling epilepsy in children with tuberous sclerosis complex: results of 7 children from a cohort of 86
M Canpolat, H Per, H Gumus, A Yikilmaz, E Unal, T Patiroglu, L Cinar, ...
Child's Nervous System 30, 227-240, 2014
472014
A case of XMEN syndrome presented with severe auto-immune disorders mimicking autoimmune lymphoproliferative disease
T Patiroglu, HH Akar, K Gilmour, E Unal, MA Ozdemir, S Bibi, S Burns, ...
Clinical immunology (Orlando, Fla.) 159 (1), 58-62, 2015
462015
Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis
AJ Walne, L Collopy, S Cardoso, A Ellison, V Plagnol, C Albayrak, ...
Haematologica 101 (10), 1180, 2016
432016
Atypical presentation of chronic granulomatous disease in an adolescent boy with frontal lobe located Aspergillus abscess mimicking intracranial tumor
T Patiroglu, E Unal, A Yikilmaz, MY Koker, MK Ozturk
Child's Nervous System 26, 149-154, 2010
432010
Intracranial hemorrhage in children with congenital factor deficiencies
T Patiroglu, MA Ozdemir, E Unal, Y Altuner Torun, A Coskun, A Menku, ...
Child's Nervous System 27, 1963-1966, 2011
422011
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