Z. Şalcıoğlu

发表

The Value of Echocardiography Versus Cardiac Troponin I levels in the Early Detection of Anthracycline Cardiotoxicity in Childhood Acute Leukemia: Prospective Evaluation of a 7-Year-Long Clinical Follow-up

S. Guler, G. Aydogan, K. Oztarhan, 2011, Pediatric hematology and oncology.

Cardiac T2* MRI assessment in patients with thalassaemia major and its effect on the preference of chelation therapy

N. Ayaz, D. Tuğcu, G. Aydogan, 2014, International Journal of Hematology.

Hepatic Focal Nodular Hyperplasia Developing after Childhood Cancers: Two-Center's Experience from Turkey

R. Kebudi, D. Tuğcu, G. Aydogan, 2014 .

Real-Time PCR analysis of af4 and dek genes expression in acute promyelocytic leukemia t (15;17)patients

B. Nagy, U. Ozbek, H. Savlı, 2004, Experimental & Molecular Medicine.

Clinical management, psychosocial characteristics, and quality of life in patients with homozygous familial hypercholesterolemia undergoing LDL-apheresis in Turkey: Results of a nationwide survey (A-HIT1 registry).

L. Tokgozoglu, L. Kaynar, M. Yılmaz, 2019, Journal of clinical lipidology.

A nation-wide survey of patients with homozygous familial hypercholesterolemia phenotype undergoing LDL-apheresis in Turkey (A-HIT 1 registry).

L. Tokgozoglu, O. O. Gul, L. Kaynar, 2018, Atherosclerosis.

What have we learned from Turkish familial hypercholesterolemia registries (A-HIT1 and A-HIT2)?

Z. Yiğit, L. Tokgozoglu, A. Oguz, 2018, Atherosclerosis.

Adrenomedullin—A New Marker in Febrile Neutropenia: Comparison With CRP and Procalcitonin

H. Ekmekçi, D. Tuğcu, G. Aydogan, 2015, Pediatric hematology and oncology.

Factor VII Deficiency

Z. Başlar, N. Ayaz, D. Tuğcu, 2012, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

A Pediatric Case of Idiopathic Hypereosinophilia Preceeding Precursor B-cell Lymphoblastic Lymphoma of Nasopharynx.

E. Yılmaz, G. Aydogan, Z. Şalcıoğlu, 2019, Journal of pediatric hematology/oncology.

Efficacy of FEIBA for acute bleeding and surgical haemostasis in haemophilia A patients with inhibitors: a multicentre registry in Turkey

K. Kavakli, G. Aydogan, T. Gursel, 2012, Haemophilia : the official journal of the World Federation of Hemophilia.

Surgical interventions in childhood rare factor deficiencies: a single-center experience from Turkey

Z. Başlar, N. Ayaz, D. Tuğcu, 2013, Blood Coagulation and Fibrinolysis.

Application of radioisotope synovectomy in the ankle joint in a child with congenital factor VII deficiency

N. Özdemir, G. Aydogan, Z. Şalcıoğlu, 2020, Turk pediatri arsivi.

Congenital Factor Deficiencies in Children: A Report of a Single-Center Experience

Z. Başlar, A. Ayçiçek, D. Tuğcu, 2017, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

How do we encounter rare factor deficiencies in children? Single-centre results from Turkey

G. Keskindemirci, Z. Başlar, N. Ayaz, 2015, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Factor 8 Gene Mutation Spectrum of 270 Patients with Hemophilia A: Identification of 36 Novel Mutations

F. Şahin, Y. Oymak, Ekrem Ünal, 2020, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Causes of Hypochromic Microcytic Anemia in Children and Evaluation of Laboratory Parameters in the Differentiation

G. Aydogan, Z. Şalcıoğlu, Cengiz Bayram, 2019, Journal of pediatric hematology/oncology.

Insidious Renal Damage in Patients with Thalassemia Major: Is it More Serious than Appreciated?

D. Tuğcu, G. Aydogan, Z. Şalcıoğlu, 2014 .

Prognostic Significance of NOTCH1 and FBXW7 Mutations in Pediatric T-ALL

T. Celkan, U. Ozbek, G. Aydogan, 2010, Disease markers.

Prognosti csignificanc eo fNOTCH1 and FBXW7 mutation si npediatri cT-ALL

T. Celkan, U. Ozbek, G. Aydogan, 2010 .