Şule Ünal Cangül

Assoc. Prof. Sule Unal

1. Oral health status of patients with inherited bone marrow failure syndromesOzler C. O., Mustuloglu S., Cemaloglu M., Dilek Turgut M., UZAMIŞ TEKÇİÇEK M., GÜMRÜK F., et al.Pediatric Dental Journal, cilt.32, sa.3, ss.151-159, 2022 (ESCI, Scopus)
2. Clinical Characteristics and Outcomes of COVID-19 in Turkish Patients with Hematological MalignanciesCİVRİZ BOZDAĞ S., CENGİZ SEVAL G., Hindilerden I. Y., Hindilerden F., ANDIÇ N., BAYDAR M., et al.TURKISH JOURNAL OF HEMATOLOGY, cilt.39, sa.1, ss.43-54, 2022 (SCI-Expanded, Scopus, TRDizin)
3. ThalassemiaAKSU T., ÜNAL CANGÜL Ş.Trends in pediatrics, cilt.2, sa.1, ss.1-7, 2021 (Scopus)
4. Central nervous system lesions in Fanconi anemia: Experience from a research center for Fanconi anemia patientsAKSU T., GÜMRÜK F., Bayhan T., Coskun C., Oguz K. K., ÜNAL Ş.PEDIATRIC BLOOD & CANCER, cilt.67, sa.12, 2020 (SCI-Expanded, Scopus)
5. Comment on: Clinical, cytogenetic, and molecular analyses of 17 neonates with transient abnormal myelopoiesis and nonconstitutional trisomy 21AKSU T., GÜMRÜK F., ÜNAL Ş.PEDIATRIC BLOOD & CANCER, cilt.67, sa.11, 2020 (SCI-Expanded, Scopus)
6. A case report of RAS-associated autoimmune lymphoproliferative disorderCOŞKUN Ç., GÜMRÜK F., CEMALOĞLU M., ORHAN M. F., TEZCAN F. İ., ÜNAL CANGÜL Ş.Hematology, Transfusion and Cell Therapy, cilt.42, sa.1, ss.28-29, 2020 (ESCI, Scopus)
7. Modelling the future of HIV in Turkey: disease implications of improving prevention, diagnosis and treatmentYaylali E., Gokengin D., Korten V., Tabak F., Unal S., Erdogan Z., et al.JOURNAL OF THE INTERNATIONAL AIDS SOCIETY, cilt.23, ss.96-97, 2020 (SCI-Expanded, Scopus)
8. Comparison of Compliance of Different Iron Chelators Including Original and Bioequivalents of DeferasiroxAKSU T., Özbek N. Y., SÖKER M., Coşkun Ç., GÜZELKÜÇÜK Z., ÜZEL V. H., et al.Acta Medica, cilt.51, sa.3, ss.38-43, 2020 (TRDizin)
9. TURKEY CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA REGISTRATION SYSTEM RESULTSAlbayrak C., Albayrak D., Oren H., Aksu T., Yarali N., Kacar D., et al.HAEMOPHILIA, cilt.26, ss.146-147, 2020 (SCI-Expanded, Scopus)
10. Outcomes of Eltrombopag Treatment and Development of Iron Deficiency in Children with Immune Thrombocytopenia in TurkeyYozgat A. K., LEBLEBİSATAN G., Akbayram S., Ozel S. C., KARAKAŞ Z., ERDURAN E., et al.TURKISH JOURNAL OF HEMATOLOGY, cilt.37, sa.3, ss.139-144, 2020 (SCI-Expanded, Scopus, TRDizin)
11. A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2Ozen S., Bilginer Y., Batu E., Taşkıran E., Özkara H. A., Ünal Ş., et al.JOURNAL OF RHEUMATOLOGY, cilt.47, sa.1, ss.117-125, 2020 (SCI-Expanded, Scopus)
12. Rare Cytogenetic Anomalies in Two Pediatric Patients with Acute LeukemiaBozkurt S., ÜNAL Ş., Bayhan T., GÜMRÜK F., Cetin M.TURKISH JOURNAL OF HEMATOLOGY, cilt.37, sa.2, ss.132-133, 2020 (SCI-Expanded, Scopus, TRDizin)
13. Infant Acute Lymphoblastic Leukemia with Atypical PresentationYAMAN BAJİN H. İ., YILDIZ Y., akın ş., AYTAÇ EYÜPOĞLU Ş. S., ÜNAL CANGÜL Ş., KUŞKONMAZ B. B., et al.Acta Medica, cilt.50, sa.4, ss.57-59, 2019 (TRDizin)
14. Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein.Russo R., Marra R., Andolfo I., De R., Rosato B., Manna F., et al.Frontiers in physiology, cilt.10, ss.621, 2019 (SCI-Expanded, Scopus)
15. Refugee children with beta-thalassemia in Turkey: Overview of demographic, socioeconomic, and medical characteristics.Yazal E., Demir Y., Pekpak E., Akıncı B., Aktekin E., Bayram C., et al.Pediatric blood & cancer, cilt.66, 2019 (SCI-Expanded, Scopus)
16. Vacuolization in myeloid and erythroid precursors in a child with menkes disease Menkes hastalıklı bir çocukta myeloid ve eritroid öncüllerde vaküolizasyonSayın S., Ünal Ş., Çetin M., Gümrük F.Turkish Journal of Hematology, cilt.36, sa.3, ss.203-204, 2019 (SCI-Expanded, Scopus, TRDizin)
17. Both Granulocytic and Non-Granulocytic Blood Cells Are Affected in Patients with Severe Congenital Neutropenia and Their Non-Neutropenic Family Members: An Evaluation of Morphology, Function, and Cell Death.Olcay L., Ünal Ş., Onay H., Erdemli E., Öztürk A., Billur D., et al.Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.35, sa.4, ss.229-259, 2018 (SCI-Expanded, Scopus, TRDizin)
18. Molecular approaches to diagnose Diamond-Blackfan anemia: The EuroDBA experience.Da C., O'Donohue M., van D., Albrecht K., Unal Ş., Ramenghi U., et al.European journal of medical genetics, cilt.61, ss.664-673, 2018 (SCI-Expanded, Scopus)
19. Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1Seo A., Steinberg-Shemer O., Unal Ş., Casadei S., Walsh T., Gumruk F., et al.PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, cilt.115, sa.20, ss.5241-5246, 2018 (SCI-Expanded, Scopus)
20. Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias.Russo R., Andolfo I., Manna F., Gambale A., Marra R., Rosato B., et al.American journal of hematology, cilt.93, ss.672-682, 2018 (SCI-Expanded, Scopus)
21. MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia.Germeshausen M., Ancliff P., Estrada J., Metzler M., Ponstingl E., Rütschle H., et al.Blood advances, cilt.2, ss.586-596, 2018 (SCI-Expanded, Scopus)
22. Assessment of Peripheral Neuropathy in Patients with β-Thalassemia via Electrophysiological Study: Reevaluation in the Era of Iron ChelatorsBayhan T., Ünal Ş., Konuşkan B., Erdem O., Karabulut E., Gümrük F.Hemoglobin, cilt.42, sa.2, ss.113-116, 2018 (SCI-Expanded, Scopus)
23. 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., et al.Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.35, ss.12-18, 2018 (SCI-Expanded, Scopus, TRDizin)
24. The clinical and laboratory evaluation of familial hemophagocytic lymphohistiocytosis and the importance of hepatic and spinal cord involvement: a single center experienceBeken B., Aytac Ş. S., Balta G., Kuskonmaz B. B., Uckan D., Unal Ş., et al.HAEMATOLOGICA, cilt.103, sa.2, ss.231-236, 2018 (SCI-Expanded, Scopus)
25. Acute myeloid leukemia in a child with dedicator of cytokinesis 8 (DOCK8) deficiencyKuşkonmaz B. B., Ayvaz D. N., Barış S., Ünal Ş., Tezcan İ., Uçkan D.PEDIATRIC BLOOD & CANCER, cilt.64, sa.12, 2017 (SCI-Expanded, Scopus)
26. Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like features.Carapito R., Konantz M., Paillard C., Miao Z., Pichot A., Leduc M., et al.The Journal of clinical investigation, cilt.127, ss.4090-4103, 2017 (SCI-Expanded, Scopus)
27. Heavy metal levels in patients with ineffective erythropoiesisBayhan T., Ünal Ş., Çırak E., Erdem O., Akay C., Gürsel O., et al.Transfusion and Apheresis Science, cilt.56, sa.4, ss.539-543, 2017 (SCI-Expanded, Scopus)
28. Rapid lung magnetic resonance imaging in children with pulmonary infection: reply to Sodhi et al.Ozcan H., Gormez A., Ozsurekci Y., Karakaya J., Oguz B., Unal Ş., et al.Pediatric radiology, cilt.47, ss.766, 2017 (SCI-Expanded, Scopus)
29. The questioning for routine monthly monitoring of proteinuria in patients with β-thalassemia on deferasirox chelationBayhan T., Ünal Ş., Ünlü O., Küçüker H., Tutal A., Karabulut E., et al.Hematology, cilt.22, sa.4, ss.248-251, 2017 (SCI-Expanded, Scopus)
30. Predictors of Suboptimal Follow-up in Pediatric Cancer Survivors.May L., Schwartz D., Frugé E., Laufman L., Holm S., Kamdar K., et al.Journal of pediatric hematology/oncology, cilt.39, 2017 (SCI-Expanded, Scopus)
31. Magnetic resonance imaging of pulmonary infection in immunocompromised children: comparison with multidetector computed tomography.Ozcan H., Gormez A., Ozsurekci Y., Karakaya J., Oguz B., Unal Ş., et al.Pediatric radiology, cilt.47, ss.146-153, 2017 (SCI-Expanded, Scopus)
32. Hypereosinophilic Syndrome: Hacettepe ExperienceTavil B., Aytaç Ş. S., Unal Ş., Kuskonmaz B. B., Gumruk F., Cetin M.JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, cilt.38, sa.7, ss.539-543, 2016 (SCI-Expanded, Scopus)
33. THE GLYCOCALYX AND TRAUMA: A REVIEWChignalia A., Yetimakman F., Christiaans S., Unal Ş., Bayrakci B., Wagener B., et al.SHOCK, cilt.45, sa.4, ss.338-348, 2016 (SCI-Expanded, Scopus)
34. Sorafenib-induced Posterior Reversible Encephalopathy Syndrome in a Child With FLT3-ITD-positive Acute Myeloid LeukemiaTavil B., Isgandarova F., Bayhan T., Unal Ş., Kuskonmaz B. B., Gumruk F., et al.JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, cilt.38, sa.3, ss.240-242, 2016 (SCI-Expanded, Scopus)
35. Successful Outcome With Fludarabine-Based Conditioning Regimen for Hematopoietic Stem Cell Transplantation From Related Donor in Fanconi Anemia: A Single Center Experience From TurkeyKuşkonmaz B. B., Ünal Ş., Bayhan T., Aytaç E., Tavil B., Çetin M., et al.PEDIATRIC BLOOD & CANCER, cilt.63, sa.4, ss.695-700, 2016 (SCI-Expanded, Scopus)
36. Effects of blood transfusion on cytokine profile and pulmonary function in patients with thalassemia majorGülhan B., Yalçın E., Ünal Ş., Oğuz B., Özçelik U., Ersöz D., et al.CLINICAL RESPIRATORY JOURNAL, cilt.10, sa.2, ss.153-162, 2016 (SCI-Expanded, Scopus)
37. The genetic basis of asymptomatic codon 8 frame-shift (HBB: C25_26delAA) β0-thalassaemia homozygotesJiang Z., Luo H., Huang S., Farrell J., Davis L., Théberge R., et al.British Journal of Haematology, cilt.172, sa.6, ss.958-965, 2016 (SCI-Expanded, Scopus)
38. Foetal and neonatal intracranial haemorrhage in term newborn infants: Hacettepe University experienceTavil B., Korkmaz A., Bayhan T., Aytaç Ş. S., Unal Ş., Kuskonmaz B. B., et al.BLOOD COAGULATION & FIBRINOLYSIS, cilt.27, sa.2, ss.163-168, 2016 (SCI-Expanded, Scopus)
39. Hypocholesterolemia A Neglected Laboratory FindingER ÖZTAŞ Y., ÜNAL CANGÜL Ş., YAŞAR Ü.Acta Medica, cilt.5, sa.1, ss.19-22, 2016 (Hakemli Dergi)
40. The European Hematology Association Roadmap for European Hematology Research: a consensus document.Engert A., Balduini C., Brand A., Coiffier B., Cordonnier C., Döhner H., et al.Haematologica, cilt.101, ss.115-208, 2016 (SCI-Expanded, Scopus)
41. Achievements in the last year and the new targetsER ÖZTAŞ Y., ÜNAL CANGÜL Ş., YAŞAR Ü.Acta Medica, cilt.5, sa.1, ss.1, 2016 (Hakemli Dergi)
42. Serum lipids in Turkish patients with β-thalassemia major and β-thalassemia minor Türk β-talasemi majör ve β-talasemi minör hastalarının serum lipidleriIşık B., Ünal Ş., Gümrük F.Turkish Journal of Hematology, cilt.33, sa.1, ss.72-73, 2016 (SCI-Expanded, Scopus, TRDizin)
43. Neonates born to mothers with immune thrombocytopenic purpura: a single-center experience of 20 yearsBayhan T., Tavil B., Korkmaz A., Ünal Ş., Hanalioğlu D., Yiğit Ş., et al.BLOOD COAGULATION & FIBRINOLYSIS, cilt.27, sa.1, ss.19-23, 2016 (SCI-Expanded, Scopus)
44. Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis.Tesi B., Lagerstedt-Robinson K., Chiang S., Ben B., Abboud M., Belen B., et al.Genome medicine, cilt.7, ss.130, 2015 (SCI-Expanded, Scopus)
45. Transcobalamin II Deficiency in Four Cases with Novel Mutations.Ünal Ş., Rupar T., Yetgin S., Yaralı N., Dursun A., Gürsel T., et al.Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.32, sa.4, ss.317-22, 2015 (SCI-Expanded, Scopus, TRDizin)
46. Immune Thrombocytopenic Purpura During Maintenance Phase of Acute Lymphoblastic Leukemia: A Rare Coexistence Requiring a High Degree of Suspicion, a Case Report and Review of the Literature.Bayhan T., Ünal Ş., Gümrük F., Çetin M.Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.32, sa.4, ss.363-6, 2015 (SCI-Expanded, Scopus, TRDizin)
47. Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense Mutations.Tesi B., Chiang S., El-Ghoneimy D., Hussein A., Langenskiöld C., Wali R., et al.Pediatric blood & cancer, cilt.62, ss.2094-100, 2015 (SCI-Expanded, Scopus)
48. An Infant With Congenital Leukemia Cutis and AML-M5 With MLL Gene Rearrangement.Bayhan T., Çiki K., Tavil B., Gümrük F., Çetin M., Ünal Ş.Journal of pediatric hematology/oncology, cilt.37, sa.7, ss.566-7, 2015 (SCI-Expanded, Scopus)
49. Biochemical markers of glucose metabolism may be used to estimate the degree and progression of iron overload in the liver and pancreas of patients with β-thalassemia major.Bas M., Gumruk F., Gonc N., Cetin M., Tuncer M., Hazırolan T., et al.Annals of hematology, cilt.94, sa.7, ss.1099-104, 2015 (SCI-Expanded, Scopus)
50. Case series of thromboembolic complications in childhood nephrotic syndrome: Hacettepe experience.Tavil B., Kara F., Topaloglu R., Aytac Ş. S., Unal Ş., Kuskonmaz B. B., et al.Clinical and experimental nephrology, cilt.19, sa.3, ss.506-13, 2015 (SCI-Expanded, Scopus)
51. Basal cell carcinoma after treatment of childhood acute lymphoblastic leukemia and concise review of the literature.Unal Ş., Cetin M., Gumruk F.Pediatric dermatology, cilt.32, sa.3, 2015 (SCI-Expanded, Scopus)
52. Iron chelation with deferasirox in a patient with de-novo ferroportin mutation.Unal Ş., Piperno A., Gumruk F.Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS), cilt.30, ss.1-3, 2015 (SCI-Expanded, Scopus)
53. Acute Megakaryoblastic Leukemia with t(1;22) Mimicking Neuroblastoma in an Infant.Gökçe M., Aytaç Ş. S., Ünal Ş., Altan İ., Gümrük F., Çetin M.Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.32, sa.1, ss.64-7, 2015 (SCI-Expanded, Scopus, TRDizin)
54. Proceedings in Acta MedicaÜNAL Ş., ER ÖZTAŞ Y., YAŞAR Ü.Acta Medica, cilt.4, sa.1, 2015 (Hakemli Dergi)
55. The hematological and molecular spectrum of α-thalassemias in Turkey: The hacettepe experience Türkiye’de alfa talasemilerin hematolojik ve moleküler spektrumu: Hacettepe deneyimiÜnal Ş., Gümrük F.Turkish Journal of Hematology, cilt.32, sa.2, ss.136-143, 2015 (SCI-Expanded, Scopus, TRDizin)
56. Molecular Analyses of Pyruvate Kinase Deficient Turkish Patients from a Single Center.Unal Ş., Gumruk F.Pediatric hematology and oncology, cilt.32, sa.5, ss.354-61, 2015 (SCI-Expanded, Scopus)
57. The first report of a homozygous codons 9/10 (+T) β-thalassemia mutation in a Turkish patient.Unal Ş., Chui D., Luo H., Okur H., Oymak Y., Gumruk F.Hemoglobin, cilt.39, sa.1, ss.66-8, 2015 (SCI-Expanded, Scopus)
58. Mean Platelet Volume can Predict Cerebrovascular Events in Patients with Sickle Cell Anemia.Celik T., Unal Ş., Ekinci O., Ozer C., Ilhan G., Oktay G., et al.Pakistan journal of medical sciences, cilt.31, ss.203-8, 2015 (SCI-Expanded, Scopus)
59. Fanconi's Anemia Effect or Sickle Cell Anemia Effect: That is the Question.Unal Ş., Chui D., Gumruk F.Hemoglobin, cilt.39, sa.4, ss.287-9, 2015 (SCI-Expanded, Scopus)
60. Bleeding and non-bleeding phenotypes in patients with GGCX gene mutations.Watzka M., Geisen C., Scheer M., Wieland R., Wiegering V., Dörner T., et al.Thrombosis research, cilt.134, sa.4, ss.856-65, 2014 (SCI-Expanded, Scopus)

All 133 on AVESİS →

1. GINS4 deficiency - an immunodeficiency syndrome with complex developmental aberrationsNieke J., Meino R., Smiers F., ÜNAL CANGÜL Ş., Klein C.56th Annual Conference of the European-Society-of-Human-Genetics (ESHG), Glasgow, İngiltere, 10 - 13 Haziran 2023, ss.452, (Özet Bildiri)
2. Klippel–Trenaunay syndrome associated with chronic myeloid leukemiaCoşkun Ç., AKSU T., GÜMRÜK F., ÜNAL CANGÜL Ş.XIth Eurasian Hematology Oncology, Türkiye, 21 - 24 Ekim 2020, (Özet Bildiri)
3. The Outcome of Modified St. Jude Total XV Protocol in Turkish Children with Newly Diagnosed Acute Lymphoblastic LeukemiaKÖSE H., AYTAÇ EYÜPOĞLU Ş. S., KUŞKONMAZ B. B., UÇKAN ÇETİNMKAYA D., ÜNAL CANGÜL Ş., GÜMRÜK F., et al.61th ASH Annuan Meeting, 7 - 10 Aralık 2019
4. Muscle strength is associated with activities and participation level in children with acute lymphoblastic leukemia undergoing consolidation therapyKabak V. Y., Ipek F., Dogan M., Uysal S. A., Unal S., Duger T.10th Eurasian Hematology Oncology Congress, İstanbul, Türkiye, 8 - 11 Ekim 2019, cilt.85, (Özet Bildiri)
5. Wait and watch, or test for anti-granulocyte antibodyCoskun C., Gumruk F., Unal S.10th Eurasian Hematology Oncology Congress, İstanbul, Türkiye, 8 - 11 Ekim 2019, cilt.85, (Özet Bildiri)
6. Cranial MRI findings of Patients with fanconi AnemiaAKSU T., GÜMRÜK F., KARLI OĞUZ H. K., BAYHAN T., coşkun ç., ÜNAL CANGÜL Ş.31st Annual Fanconi anemia research fund scientific symposium, Chicago, Amerika Birleşik Devletleri, 19 - 22 Eylül 2019, (Tam Metin Bildiri)
7. Influence of Paroxysmal Nocturnal Hemoglobinuria Clone Positivity on Outcome of Childhood Acquired Aplastic Anemia: A Multicenter Center StudyÜNAL CANGÜL Ş., YILMAZ KARAPINAR D., Erdem A. Y., Yarali H. N., Ozdemir H. H., GÜMRÜK F., et al.60th Annual Meeting of the American-Society-of-Hematology (ASH), California, Amerika Birleşik Devletleri, 1 - 04 Aralık 2018, cilt.132, (Özet Bildiri)
8. Childhood leukemia in an ETV6-related Thrombocytopenia family.YAMAN BAJİN H. İ., AYTAÇ EYÜPOĞLU Ş. S., KUŞKONMAZ B. B., ÜNAL CANGÜL Ş., OKUR F. V., ÇETİNKAYA F. D., et al.49th Congress of the International Society of Pediatric Oncology (SIOP), Washington, Kiribati, 12 - 15 Ekim 2017, cilt.64, ss.192, (Özet Bildiri)
9. Tyrosine Kinase Inhibitor Responses in Pediatric CML Patients: Hacettepe ExperienceYAMAN BAJİN H. İ., AYTAÇ EYÜPOĞLU Ş. S., KUŞKONMAZ B. B., ÜNAL CANGÜL Ş., OKUR F. V., ÇETİNKAYA F. D., et al.49th Congress of the International Society of Paediatric Oncology (SIOP) Washington, DC, USA October 12–15, 2017, Washington, Kiribati, 12 - 15 Ekim 2017, cilt.64, ss.202, (Özet Bildiri)
10. A Rare Cause of EBV related Familial HLH CD27 DeficiencyÜNAL CANGÜL Ş., GÜMRÜK F., TEZCAN F. İ., ÇAĞDAŞ AYVAZ D. N., ÇETİN M.ESID 2016, 21 - 24 Eylül 2016, (Özet Bildiri)
11. A rare cause of EBV related familial CD27 deficiencyÜNAL CANGÜL Ş., GÜMRÜK F., TEZCAN F. İ., ÇAĞDAŞ AYVAZ D. N., ÇETİN M.17 ESİD, 20 - 24 Eylül 2016, (Özet Bildiri)
12. The Absence of Somatic Defects in Fanconi Anemia is Not Indicative for the Absence of Bone Marrow FailureALTAN İ., ÜNAL CANGÜL Ş., BAYHAN T., ÜTİNE G. E., GÜMRÜK F.Fanconi Anemia Research FundScientific Symposium September 15-18, Bellevue, Washington, USA, 15 - 18 Eylül 2016, (Özet Bildiri)
13. Pediatrik hematopoietik kök hücre nakli sonrasında görülen dirençli sitopenilerin rituksimab ile tedavi sonuçlarıAKSU T., KUŞKONMAZ B. B., OKUR F. V., ÜNAL CANGÜL Ş., ÇETİNKAYA F. D.9. Ulusal Kemik İliği Transplantasyonu ve Kök Hücre Tedavileri Kongresi, 03 Mart 2016, (Özet Bildiri)
14. Hematopoietic stem cell transplantation in patients with genetic hemophagocytic lymphohistiocytosisKUŞKONMAZ B. B., AYTAÇ EYÜPOĞLU Ş. S., ÇAĞDAŞ AYVAZ D. N., BAYHAN T., TAVİL E. B., ÜNAL Ş., et al.41 st Annual Meeting of the European Society for Blood and Marrow Transplantation, 22-25 March 2015, İstanbul, Turkey, 22 - 25 Mart 2015, (Özet Bildiri)
15. Mitokondriyal sitopati ile ilişkili fokal segmental glomeruloskleroz Podosit ince yapısı ağırlıklı iki olgu sunumuGÜÇER K. Ş., TALİM B., AŞAN E., KORKUSUZ P., ÖZEN S., ÜNAL Ş.17. Ulusal Elektronmikroskobi kongresi. Uluslararası katılımlı, Türkiye, 22 - 24 Haziran 2005, (Özet Bildiri)
16. Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference: Interactive e-PostersGÜREL A., ÜNAL CANGÜL Ş., Yaralı N., ŞİMŞEK KİPER P. Ö., CEYLANER S., Bilir O. A., et al.
17. Occurence of acute myeloid leukemia after primary hepatic carcinoma in a patient who had liver transplantationCOŞKUN Ç., ÜNAL CANGÜL Ş., ÜNER A., AKSU T., AYTAÇ EYÜPOĞLU Ş. S., KUŞKONMAZ B. B., et al.
18. Pyruvate Kinase Deficiency Cases Mimicking Congenital Dyserythropoietic AnemiaÜNAL CANGÜL Ş., AKSU T., Coşkun Ç., GÜMRÜK F.
19. AB0574 A MONOGENIC DISEASE WITH WIDE RANGE OF SYMPTOMS: DEFICIENCY OF ADENOSINE DEAMINASE 2BATU AKAL E. D., TAŞKIRAN Z. E., TEZCAN F. İ., ÖZKARA H. A., ÇAĞDAŞ AYVAZ D. N., ÖZEN S., et al.

1. Nötropeninin Nadir Bir Nedeni: Bileşik Heterozigot Mutasyonu Olan Shwachman-Diamond SendromuAKSU T., AKARSU A. N., ÜNAL CANGÜL Ş.Olgularla Kemik İliği Yetmezlikleri, Şule Ünal Cangül, Didem Atay, Turan Bayhan, Yusuf Ziya Aral, Editör, Galenos Yayın Evi, ss.171-173, 2023
2. CTC1 Mutasyonu İlişkili İzole Kalıtsal Kemik İliği Yetmezliği OlgusuAKSU T., ÜNAL CANGÜL Ş.Olgularla Kemik İliği Yetmezlikleri, Şule Ünal Cangül, Didem Atay, Turan Bayhan, Yusuf Ziya Aral, Editör, Galenos Yayın Evi, ss.59-61, 2023
3. Diamond-Blackfan Anemisi ile İlişkili Osteosarkom OlgusuCoşkun Ç., AKSU T., GÜMRÜK F., ÜNAL CANGÜL Ş.Olgularla Kemik İliği Yetmezlikleri, Şule Ünal Cangül, Didem Atay, Turan Bayhan, Yusuf Ziya Aral, Editör, Galenos Yayın Evi, ss.24-25, 2023
4. HemoglobinopatilerAKSU T., ÜNAL CANGÜL Ş.Pediatri, Zülfikar Akelma, Editör, Ankara Nobel Tıp Kitabevleri Ltd. Şti., Ankara, ss.949-954, 2021