Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 184

1.

Outcomes and treatment strategies for autoimmunity and hyperinflammation in patients with RAG deficiency.

Farmer JR, Foldvari Z, Ujhazi B, De Ravin SS, Chen K, Bleesing JJH, Schuetz C, Al-Herz W, Abraham RS, Joshi AY, Costa-Carvalho BT, Buchbinder D, Booth C, Reiff A, Ferguson PJ, Aghamohammadi A, Abolhassani H, Puck JM, Adeli M, Cancrini C, Palma P, Bertaina A, Locatelli F, Di Matteo G, Geha RS, Kanariou MG, Lycopoulou E, Tzanoudaki M, Sleasman JW, Parikh S, Pinero G, Fischer BM, Dbaibo G, Unal E, Patiroglu T, Karakukcu M, Al-Saad KK, Dilley MA, Pai SY, Dutmer CM, Gelfand EW, Geier CB, Eibl MM, Wolf HM, Henderson LA, Hazen MM, Bonfim C, Wolska-Kuśnierz B, Butte MJ, Hernandez JD, Nicholas SK, Stepensky P, Chandrakasan S, Miano M, Westermann-Clark E, Goda V, Kriván G, Holland SM, Fadugba O, Henrickson SE, Ozen A, Karakoc-Aydiner E, Baris S, Kiykim A, Bredius R, Hoeger B, Boztug K, Pashchenko O, Neven B, Moshous D, Villartay JP, Bousfiha AA, Hill HR, Notarangelo LD, Walter JE.

J Allergy Clin Immunol Pract. 2019 Mar 12. pii: S2213-2198(19)30260-0. doi: 10.1016/j.jaip.2019.02.038. [Epub ahead of print]

PMID:
30877075
2.

Intracranial abscess developed after ganciclovir treatment: A case report.

Cansever M, Ozmansur EN, Ozcan A, Kahraman ZF, Patiroglu T.

North Clin Istanb. 2018 Aug 9;5(4):353-356. doi: 10.14744/nci.2017.13284. eCollection 2018.

3.

Hepatosplenic Fungal Infections in Children With Leukemia-Risk Factors and Outcome: A Multicentric Study.

Celkan T, Kizilocak H, Evim M, Meral Güneş A, Özbek NY, Yarali N, Ünal E, Patiroğlu T, Yilmaz Karapinar D, Sarper N, Zengin E, Karaman S, Koçak Ü, Kürekçi E, Özdemir C, Tuğcu D, Uysalol E, Dikme G, Adaletli İ, Kuruoğlu S, Kebudi R.

J Pediatr Hematol Oncol. 2019 Feb 5. doi: 10.1097/MPH.0000000000001431. [Epub ahead of print]

PMID:
30730381
4.

Evaluation of childhood solid pseudopapillary tumors of the pancreas.

Ozcan A, Arslanoglu C, Unal E, Patiroglu T, Ozdemir MA, Deniz K, Ozcan SS, Karakukcu M.

North Clin Istanb. 2018 Sep;5(3):207-210. doi: 10.14744/nci.2017.27443.

5.

A mummy emerges from the grave: Scurvy confounding the clinical presentation of a child with Fanconi anemia.

Ozcan A, Saracoglu S, Verboon JM, Karakukcu M, Patiroglu T, Coskun A, Sankaran VG, Unal E.

Am J Hematol. 2019 Apr;94(4):506-507. doi: 10.1002/ajh.25402. Epub 2019 Jan 25. No abstract available.

PMID:
30637794
6.

Proteome analysis of human neutrophil granulocytes from patients with monogenic disease using data-independent acquisition.

Grabowski P, Hesse S, Hollizeck S, Rohlfs M, Behrends U, Sherkat R, Tamary H, Ünal E, Somech R, Patıroğlu T, Canzar S, van der Werff Ten Bosch J, Klein C, Rappsilber J.

Mol Cell Proteomics. 2019 Jan 10. pii: mcp.RA118.001141. doi: 10.1074/mcp.RA118.001141. [Epub ahead of print]

7.

Underlying factors of recurrent infections in patients with down syndrome.

Patiroglu T, Cansever M, Bektas F.

North Clin Istanb. 2018 Jan 29;5(2):163-168. doi: 10.14744/nci.2017.69379. eCollection 2018. Review.

8.

Fanconi Anemia and Ataxia Telangiectasia in Siblings who Inherited Unique Combinations of Novel FANCA and ATM Null Mutations.

Balta G, Patiroglu T, Gumruk F.

J Pediatr Hematol Oncol. 2019 Apr;41(3):243-246. doi: 10.1097/MPH.0000000000001336.

PMID:
30339652
9.

Deferasirox in children with transfusion-dependent thalassemia or sickle cell anemia: A large cohort real-life experience from Turkey (REACH-THEM).

Antmen B, Karakaş Z, Yeşilipek MA, Küpesiz OA, Şaşmaz İ, Uygun V, Kurtoğlu E, Oktay G, Aydogan G, Akın M, Salcioglu Z, Vergin C, Kazancı EG, Ünal S, Çalışkan Ü, Aral YZ, Türkkan E, Meral Güneş A, Tunç B, Gümrük F, Ayhan AC, Söker M, Koç A, Oymak Y, Ertem M, Timur Ç, Yıldırmak Y, İrken G, Apak H, Biner B, Eren TG, Işık Balcı Y, Koçak Ü, Karasu G, Akkaynak D, Patıroğlu T.

Eur J Haematol. 2019 Feb;102(2):123-130. doi: 10.1111/ejh.13180. Epub 2018 Dec 9.

PMID:
30300449
10.

Correction to: Novel Mutations in RASGRP1 Are Associated with Immunodeficiency, Immune Dysregulation, and EBV-Induced Lymphoma.

Somekh I, Marquardt B, Liu Y, Rohlfs M, Hollizeck S, Karakukcu M, Unal E, Yilmaz E, Patiroglu T, Cansever M, Frizinsky S, Vishnvenskia-Dai V, Rechavi E, Stauber T, Simon AJ, Lev A, Klein C, Kotlarz D, Somech R.

J Clin Immunol. 2018 Aug;38(6):711. doi: 10.1007/s10875-018-0541-8.

PMID:
30099695
11.

Novel Mutations in RASGRP1 are Associated with Immunodeficiency, Immune Dysregulation, and EBV-Induced Lymphoma.

Somekh I, Marquardt B, Liu Y, Rohlfs M, Hollizeck S, Karakukcu M, Unal E, Yilmaz E, Patiroglu T, Cansever M, Frizinsky S, Vishnvenska-Dai V, Rechavi E, Stauber T, Simon AJ, Lev A, Klein C, Kotlarz D, Somech R.

J Clin Immunol. 2018 Aug;38(6):699-710. doi: 10.1007/s10875-018-0533-8. Epub 2018 Jul 20. Erratum in: J Clin Immunol. 2018 Aug 11;:.

PMID:
30030704
12.

Biliary Rhabdomyosarcoma in an Infant Male With Neurofibromatosis Type 1.

Alhashem F, Yilmaz E, Ozdemir MA, Deniz K, Yikilmaz A, Patiroglu T, Karakukcu M, Unal E.

J Pediatr Hematol Oncol. 2019 Jan;41(1):e24-e26. doi: 10.1097/MPH.0000000000001163.

PMID:
29683957
13.

Cerebral Sinus Venous Thrombosis and Prothrombotic Risk Factors in Children: A Single-Center Experience From Turkey.

Ozcan A, Canpolat M, Doganay S, Unal E, Karakukcu M, Ozdemir MA, Patiroglu T.

J Pediatr Hematol Oncol. 2018 Aug;40(6):e369-e372. doi: 10.1097/MPH.0000000000001149.

PMID:
29668537
14.

Results of the Hematology Laboratory Survey: What has Changed in Eight Years?

Kozanoğlu İ, Patıroğlu T, Dalva K, Yanıkkaya Demirel G, Soysal T, Demir M.

Turk J Haematol. 2018 Aug 3;35(3):215-216. doi: 10.4274/tjh.2018.0065. Epub 2018 Apr 18. No abstract available.

15.

Effectiveness of Ankaferd BloodStopper in Prophylaxis and Treatment of Oral Mucositis in Childhood Cancers Evaluated with Plasma Citrulline Levels.

Patıroğlu T, Erdoğ Şahin N, Ünal E, Kendirci M, Karakükcü M, Özdemir MA.

Turk J Haematol. 2018 Mar 1;35(1):85-86. doi: 10.4274/tjh.2017.0320. Epub 2018 Feb 2. No abstract available.

16.

The relationship between hematological parameters and prognosis of children with acute ischemic stroke.

Yilmaz E, Bayram Kacar A, Bozpolat A, Zararsiz G, Gorkem BS, Karakukcu M, Patiroglu T, Gumus H, Ozdemir MA, Ozcan A, Per H, Unal E.

Childs Nerv Syst. 2018 Apr;34(4):655-661. doi: 10.1007/s00381-017-3673-x. Epub 2017 Dec 5.

PMID:
29209887
17.

A Case of Familial Hemophagocytic Lymphohistiocytosis Type 4 With Involvement of the Central Nervous System Complicated With Infarct.

Ciraci S, Ozcan A, Ozdemir MM, Chiang SCC, Tesi B, Ozdemir AM, Karakukcu M, Patiroglu T, Acipayam C, Doganay S, Gumus H, Unal E.

J Pediatr Hematol Oncol. 2017 Aug;39(6):e321-e324. doi: 10.1097/MPH.0000000000000886.

PMID:
28692549
18.

Differences in Granule Morphology yet Equally Impaired Exocytosis among Cytotoxic T Cells and NK Cells from Chediak-Higashi Syndrome Patients.

Chiang SCC, Wood SM, Tesi B, Akar HH, Al-Herz W, Ammann S, Belen FB, Caliskan U, Kaya Z, Lehmberg K, Patiroglu T, Tokgoz H, Ünüvar A, Introne WJ, Henter JI, Nordenskjöld M, Ljunggren HG, Meeths M, Ehl S, Krzewski K, Bryceson YT.

Front Immunol. 2017 Apr 18;8:426. doi: 10.3389/fimmu.2017.00426. eCollection 2017.

19.

A National Registry of Thalassemia in Turkey: Demographic and Disease Characteristics of Patients, Achievements, and Challenges in Prevention.

Aydınok Y, Oymak Y, Atabay B, Aydoğan G, Yeşilipek A, Ünal S, Kılınç Y, Oflaz B, Akın M, Vergin C, Sezgin Evim M, Çalışkan Ü, Ünal Ş, Bay A, Kazancı E, İleri T, Atay D, Patıroğlu T, Kahraman S, Söker M, Akcan M, Akdeniz A, Büyükavcı M, Alanoğlu G, Bör Ö, Soyer N, Özdemir Karadaş N, Uysalol E, Türker M, Akçay A, Ocak S, Güneş AM, Tokgöz H, Ünal E, Tiftik N, Karakaş Z.

Turk J Haematol. 2018 Mar 1;35(1):12-18. doi: 10.4274/tjh.2017.0039. Epub 2017 Apr 13.

20.

Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO Mutation.

Kim AR, Ulirsch JC, Wilmes S, Unal E, Moraga I, Karakukcu M, Yuan D, Kazerounian S, Abdulhay NJ, King DS, Gupta N, Gabriel SB, Lander ES, Patiroglu T, Ozcan A, Ozdemir MA, Garcia KC, Piehler J, Gazda HT, Klein DE, Sankaran VG.

Cell. 2017 Mar 9;168(6):1053-1064.e15. doi: 10.1016/j.cell.2017.02.026.

21.

Juvenile Myelomonocytic Leukemia in Turkey: A Retrospective Analysis of Sixty-five Patients.

Tüfekçi Ö, Koçak Ü, Kaya Z, Yenicesu İ, Albayrak C, Albayrak D, Yılmaz Bengoa Ş, Patıroğlu T, Karakükçü M, Ünal E, Ünal İnce E, İleri T, Ertem M, Celkan T, Özdemir GN, Sarper N, Kaçar D, Yaralı N, Özbek NY, Küpesiz A, Karapınar T, Vergin C, Çalışkan Ü, Tokgöz H, Sezgin Evim M, Baytan B, Güneş AM, Yılmaz Karapınar D, Karaman S, Uygun V, Karasu G, Yeşilipek MA, Koç A, Erduran E, Atabay B, Öniz H, Ören H.

Turk J Haematol. 2018 Mar 1;35(1):27-34. doi: 10.4274/tjh.2017.0021. Epub 2017 Feb 9.

22.

Neuroblastoma in a Child With Wolf-Hirschhorn Syndrome.

Ozcan A, Acer H, Ciraci S, Gumus H, Karakukcu M, Patiroglu T, Ozdemir MA, Unal E.

J Pediatr Hematol Oncol. 2017 May;39(4):e224-e226. doi: 10.1097/MPH.0000000000000768.

PMID:
28085742
23.

Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency.

Lévy R, Okada S, Béziat V, Moriya K, Liu C, Chai LY, Migaud M, Hauck F, Al Ali A, Cyrus C, Vatte C, Patiroglu T, Unal E, Ferneiny M, Hyakuna N, Nepesov S, Oleastro M, Ikinciogullari A, Dogu F, Asano T, Ohara O, Yun L, Della Mina E, Bronnimann D, Itan Y, Gothe F, Bustamante J, Boisson-Dupuis S, Tahuil N, Aytekin C, Salhi A, Al Muhsen S, Kobayashi M, Toubiana J, Abel L, Li X, Camcioglu Y, Celmeli F, Klein C, AlKhater SA, Casanova JL, Puel A.

Proc Natl Acad Sci U S A. 2016 Dec 20;113(51):E8277-E8285. doi: 10.1073/pnas.1618300114. Epub 2016 Dec 7.

24.

Fibromuscular Dysplasia Complicated With Cerebral Stroke in a Child With Congenital Dyserythropoietic Anemia Type II.

Ozcan A, Patiroglu T, Acer H, Gumus H, Senol S, Karakukcu M, Ozdemir MA, Unal E.

J Pediatr Hematol Oncol. 2016 Nov;38(8):e333-e335.

PMID:
27548341
25.

Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis.

Walne AJ, Collopy L, Cardoso S, Ellison A, Plagnol V, Albayrak C, Albayrak D, Kilic SS, Patıroglu T, Akar H, Godfrey K, Carter T, Marafie M, Vora A, Sundin M, Vulliamy T, Tummala H, Dokal I.

Haematologica. 2016 Oct;101(10):1180-1189. Epub 2016 Sep 9.

26.

Dermatological Findings in Turkish Paediatric Haematology-Oncology Patients.

Uksal U, Ozturk P, Colgecen E, Taslidere N, Patiroglu T, Ozdemir MA, Torun YA, Borlu M.

Eurasian J Med. 2016 Jun;48(2):107-11. doi: 10.5152/eurasianjmed.2015.86.

27.

DOCK8 deficiency in a boy who presented with a giant aortic aneurysm between aortic root and iliac bifurcation.

Patıroğlu T, Akar HH, Doğan MS, Üzüm K.

Turk Kardiyol Dern Ars. 2016 Jun;44(4):342-5. doi: 10.5543/tkda.2015.26511.

28.

XLF deficiency results in reduced N-nucleotide addition during V(D)J recombination.

IJspeert H, Rozmus J, Schwarz K, Warren RL, van Zessen D, Holt RA, Pico-Knijnenburg I, Simons E, Jerchel I, Wawer A, Lorenz M, Patıroğlu T, Akar HH, Leite R, Verkaik NS, Stubbs AP, van Gent DC, van Dongen JJ, van der Burg M.

Blood. 2016 Aug 4;128(5):650-9. doi: 10.1182/blood-2016-02-701029. Epub 2016 Jun 8.

29.

PARTIAL OCULOCUTANEOUS ALBINISM AND IMMUNODEFICIENCY SYNDROMES: TEN YEARS EXPERIENCE FROM A SINGLE CENTER IN TURKEY.

Patiroglu T, Akar HH, Unal E, Chiang SC, Schlums H, Tesi B, Ozkars MY, Karakukcu M.

Genet Couns. 2016;27(1):67-76.

PMID:
27192893
30.

CLINICAL FEATURES AND GENETIC ANALYSIS OF SIX PATIENTS WITH WISKOTT-ALDRICH SYNDROME REPORTING TWO NOVEL MUTATIONS: EXPERIENCE OF ERCIYES UNIVERSITY, KAYSERI, TURKEY.

Patiroglu T, Klein C, Gungor HE, Ozdemir MA, Witzel M, Karakukcu M, Sawalle-Belohradsky J, Conca R, Unal E.

Genet Couns. 2016;27(1):9-24.

PMID:
27192888
31.

Combined immunodeficiencies: twenty years experience from a single center in Turkey.

Akar HH, Patiroglu T, Hershfield M, van der Burg M.

Cent Eur J Immunol. 2016;41(1):107-15. doi: 10.5114/ceji.2015.56168. Epub 2016 Jan 20.

32.

The Frequency of HLA-A, HLA-B, and HLA-DRB1 Alleles in Patients with Acute Lymphoblastic Leukemia in the Turkish Population: A Case-Control Study.

Patıroğlu T, Akar HH.

Turk J Haematol. 2016 Dec 1;33(4):339-345. doi: 10.4274/tjh.2016.0102. Epub 2016 Apr 18.

33.

Hematopoietic Stem Cell Transplant for Primary Immunodeficiency Diseases: A Single-Center Experience.

Patiroglu T, Akar HH, Unal E, Ozdemir MA, Karakukcu M.

Exp Clin Transplant. 2017 Jun;15(3):337-343. doi: 10.6002/ect.2015.0233. Epub 2016 Mar 21.

34.

Nonacog beta pegol (N9-GP) in haemophilia B: A multinational phase III safety and efficacy extension trial (paradigm™4).

Young G, Collins PW, Colberg T, Chuansumrit A, Hanabusa H, Lentz SR, Mahlangu J, Mauser-Bunschoten EP, Négrier C, Oldenburg J, Patiroglu T, Santagostino E, Tehranchi R, Zak M, Karim FA.

Thromb Res. 2016 May;141:69-76. doi: 10.1016/j.thromres.2016.02.030. Epub 2016 Mar 2.

PMID:
26970716
35.

Three faces of recombination activating gene 1 (RAG1) mutations.

Patiroglu T, Akar HH, Van Der Burg M.

Acta Microbiol Immunol Hung. 2015 Dec;62(4):393-401. doi: 10.1556/030.62.2015.4.4.

PMID:
26689875
36.

Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis.

Tesi B, Lagerstedt-Robinson K, Chiang SC, Ben Bdira E, Abboud M, Belen B, Devecioglu O, Fadoo Z, Yeoh AE, Erichsen HC, Möttönen M, Akar HH, Hästbacka J, Kaya Z, Nunes S, Patiroglu T, Sabel M, Saribeyoglu ET, Tvedt TH, Unal E, Unal S, Unuvar A, Meeths M, Henter JI, Nordenskjöld M, Bryceson YT.

Genome Med. 2015 Dec 18;7:130. doi: 10.1186/s13073-015-0244-1.

37.

The Importance of Nucleated Red Blood Cells in Patients with Beta Thalassemia Major and Comparison of Two Automated Systems with Manual Microscopy and Flow Cytometry.

Karakukcu M, Karakukcu C, Unal E, Ozturk A, Ciraci Z, Patiroglu T, Ozdemir MA.

Clin Lab. 2015;61(9):1289-95.

PMID:
26554249
38.

Autosomal recessive hyper IgM syndrome associated with activation-induced cytidine deaminase gene in three Turkish siblings presented with tuberculosis lymphadenitis - Case report.

Patiroglu T, Akar HH, van der Burg M, Unal E.

Acta Microbiol Immunol Hung. 2015 Sep;62(3):267-74. doi: 10.1556/030.62.2015.3.4.

PMID:
26551569
39.
41.
42.

A case of XLF deficiency presented with diffuse large B cell lymphoma in the brain.

Patiroglu T, Akar HH, van der Burg M, Kontas O.

Clin Immunol. 2015 Dec;161(2):394-5. doi: 10.1016/j.clim.2015.06.009. Epub 2015 Jun 26. No abstract available.

PMID:
26119972
43.

Regression of steatohepatitis-related cirrhosis.

Deniz K, Özcan S, Özbakır Ö, Patıroğlu TE.

Semin Liver Dis. 2015 May;35(2):199-202. doi: 10.1055/s-0035-1550058. Epub 2015 May 14.

PMID:
25974904
44.

A case of XMEN syndrome presented with severe auto-immune disorders mimicking autoimmune lymphoproliferative disease.

Patiroglu T, Haluk Akar H, Gilmour K, Unal E, Akif Ozdemir M, Bibi S, Burns S, Chiang SC, Schlums H, Bryceson YT, Karakukcu M.

Clin Immunol. 2015 Jul;159(1):58-62. doi: 10.1016/j.clim.2015.04.015. Epub 2015 May 6. No abstract available.

PMID:
25956530
45.

Silent brain infarcts in two patients with zeta chain-associated protein 70 kDa (ZAP70) deficiency.

Akar HH, Patiroglu T, Akyildiz BN, Tekerek NU, Doğan MS, Doğanay S, van der Burg M, Dusunsel R.

Clin Immunol. 2015 May;158(1):88-91. doi: 10.1016/j.clim.2015.03.014. Epub 2015 Mar 22.

PMID:
25805655
46.

X-linked agammaglobulinemia in two siblings with a novel mutation in the BTK gene who presented with polyarticular juvenile idiopathic arthritis.

Patiroglu T, Akar HH, Gunduz Z, Sisko S, Ng YY.

Scand J Rheumatol. 2015;44(2):168-70. doi: 10.3109/03009742.2014.995699. No abstract available.

PMID:
25757060
47.

The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.

Engelhardt KR, Gertz ME, Keles S, Schäffer AA, Sigmund EC, Glocker C, Saghafi S, Pourpak Z, Ceja R, Sassi A, Graham LE, Massaad MJ, Mellouli F, Ben-Mustapha I, Khemiri M, Kilic SS, Etzioni A, Freeman AF, Thiel J, Schulze I, Al-Herz W, Metin A, Sanal Ö, Tezcan I, Yeganeh M, Niehues T, Dueckers G, Weinspach S, Patiroglu T, Unal E, Dasouki M, Yilmaz M, Genel F, Aytekin C, Kutukculer N, Somer A, Kilic M, Reisli I, Camcioglu Y, Gennery AR, Cant AJ, Jones A, Gaspar BH, Arkwright PD, Pietrogrande MC, Baz Z, Al-Tamemi S, Lougaris V, Lefranc G, Megarbane A, Boutros J, Galal N, Bejaoui M, Barbouche MR, Geha RS, Chatila TA, Grimbacher B.

J Allergy Clin Immunol. 2015 Aug;136(2):402-12. doi: 10.1016/j.jaci.2014.12.1945. Epub 2015 Feb 25.

48.

A case of congenital afibrinogenemia complicated with thromboembolic events that required repeated amputations.

Ozdemir MA, Işik B, Patiroglu T, Karakukcu M, Mutlu FT, Yilmaz E, Unal E.

Blood Coagul Fibrinolysis. 2015 Apr;26(3):354-6. doi: 10.1097/MBC.0000000000000200.

PMID:
25255238
49.

Brain abscesses in children: results of 24 children from a reference center in Central Anatolia, Turkey.

Canpolat M, Ceylan O, Per H, Koc G, Tumturk A, Kumandas S, Patiroglu T, Doganay S, Gumus H, Unal E, Kose M, Gorkem SB, Kurtsoy A, Ozturk MK.

J Child Neurol. 2015 Mar;30(4):458-67. doi: 10.1177/0883073814549247. Epub 2014 Sep 15.

PMID:
25223695
50.

X-linked severe combined immunodeficiency due to a novel mutation complicated with hemophagocytic lymphohistiocytosis and presented with invagination: A case report.

Patiroglu T, Haluk Akar H, van den Burg M, Unal E, Akyildiz BN, Tekerek NU, Yilmaz E.

Eur J Microbiol Immunol (Bp). 2014 Sep;4(3):174-6. doi: 10.1556/EUJMI-D-14-00019. Epub 2014 Sep 11.

Supplemental Content

Loading ...
Support Center