Poster NO
|
Name
|
Surname
|
Abstract Title
|
PP-01
|
MIRELDAR
|
BABAYEV
|
SUCCESSES IN THE FIELD OF CHILD'S LEUKOSOLOGY IN AZERBAIJAN
|
PP-02
|
ALINA
|
ANTIPOVA
|
A RARE TYPE OF MIXED PHENOTYPE ACUTE LEUKEMIA
T/B-LYMPHOID/MEGAKARYOBLASTIC
|
PP-03
|
MAHMUD
|
MAHMUDOV
|
THE STUDY OF QUALITY OF LIFE IN VARIOUS VARIANTS OF ACUTE
LEUKEMIA PATIENTS
|
PP-04
|
SHAD
|
AHMED
|
HERITBLE RUNX1 AND GATA2 MUTATION WITH A VERY RARE GENE VARIANT
ASSOCIATED WITH AML-MDS: A CASE REPORT AND REVIEW OF LITERATURE
|
PP-05
|
RAFİYE
|
ÇİFTÇİLER
|
SAFETY AND EFFICACY OF DIFFERENT ARA-C REGIMENS DURING THE
CLINICAL COURSE OF ACUTE MYELOID LEUKEMIA
|
PP-06
|
MOUSSAB
|
DAMLAJ
|
ROLE OF ALLOGENEIC HCT AS POST REMISSION THERAPY FOR ADULT
LYMPHOBLASTIC LEUKEMIA / LYMPHOMA FOLLOWING FRONT LINE
HYPERCVAD
|
PP-07
|
PINAR
|
CÖMERT
|
A RARE PRESENTATION OF RECURRENCE IN ACUTE LYMPHOBLASTIC
LEUKEMIA: ISOLATED OPTIC NERVE INVOLVEMENT
|
PP-08
|
SİNAN
|
DEMİRCİOĞLU
|
MUCORMYCOSIS IN A PATIENT WITH ACUTE LYMPHOBLASTIC LEUKEMIA: A
CASE REPORT
|
PP-09
|
ESRA
|
TERZI DEMIRSOY
|
A RARE ENTITY:PHILADELPHIA-POSITIVE ACUTE MYELOBLASTIC LEUKEMIA
WITH P190 FUSION PROTEIN
|
PP-10
|
GHADA
|
ELGOHARY
|
MOLECULAR PROFILE OF HEMOGLOBINOPATHY MUTATIONS IN KING KHALID
UNIVERSITY HOSPITAL: A SINGLE CENTER EXPERIENCE
|
PP-11
|
NASER SHAGERDI
|
ESMAELI
|
IRON DEFICIENCY AND IT’S LEVEL IN IRANIAN PREGNANT WOMEN
|
PP-12
|
MÜRÜVVET SEDA
|
AYDIN
|
IS HEREDITARY STOMATOCYTOSIS A RARE ERYTHROCYTE MEMBRANE
DISORDER OR AN OVERLOOKED ITEM?
|
PP-13
|
ANIL
|
TOMBAK
|
IS L-GLUTAMINE REALLY EFFECTIVE IN REDUCING PAINFULL CRISIS AND
HOSPITALIZATION FOR SICKLE CELL ANEMIA PATIENTS IN REAL LIFE?
|
PP-14
|
PINAR
|
CÖMERT
|
INTERMITTENT BEVACIZUMAB THERAPY EXPERIENCE IN HEREDITARY
HEMORRHAGIC TELANGIECTASIA
|
PP-15
|
ÖMER
|
EKİNCİ
|
COMPLEMENT-MEDIATED HEMOLYTIC UREMIC SYNDROME: A CASE REPORT
|
PP-16
|
ÖMER
|
EKİNCİ
|
CLINICAL FEATURES AND RESPONSES TO ECULIZUMAB OF PAROXYSMAL
NOCTURNAL HEMOGLOBINURIA PATIENTS: A SINGLE-CENTER EXPERIENCE
|
PP-17
|
MEMDUH
|
ŞAHİN
|
EVALUATION OF THE EFFECTS OF IRON DEFICIENCY ANEMIC TREATMENT
IN BLOOD LIPID LEVELS AND BODY MEASUREMENTS IN MIDDLE AGE AND
ADELOSAN WOMEN
|
PP-18
|
MONA
|
ALFARAJ
|
HUMAN PARVOVIRUS B19 AND BLOOD PRODUCT SAFETY: CURRENT AND
FURTHER PERSPECTIVES.
|
PP-19
|
ENGİN
|
KELKİTLİ
|
EVALUATION OF AUTOIMMUNE HEMOLYTIC ANEMIA PATIENTS AFTER
SPLENECTOMY SINGLE CENTRE EXPERIENCE
|
PP-20
|
RABBİA
|
LATİF
|
SPECTRUM OF BANE MARROW CHANGES IN ADVANCE STAGE CHRONIC KIDNEY
DISEASE
|
PP-21
|
SALİH
|
DURUSOY
|
LATE DIAGNOSIS IN SYRIAN IMMIGRANT PATIENT; THIAMINE-RESPONSIVE
MEGALOBLASTIC ANEMIA SYNDROME
|
PP-22
|
MERAL
|
ILGAZ ERGIN
|
AUTOLOGOUS STEM CELL TRANSPLANTATION AND CMV
|
PP-23
|
RAFİYE
|
ÇİFTÇİLER
|
EXTRAMEDULLARY RELAPSE OF THE AML FOLLOWİNG ALLO-HSCT: A CASE
REPORT
|
PP-24
|
NASER
|
ESMAELI
|
EVALUATION OF HEMOGLOBIN LEVELS WITH CLINICAL OUTCOME IN
PATIENTS UNDERGOING HEMATOPOIETIC STEM CELL TRANSPLANTATION
|
PP-25
|
MONA
|
HASSANEIN
|
A CASE OF APLASTIC ANEMIA WITH GRAFT FAILURE AND AUTOLOGOUS
RECOVERY POST ALLOGENIC STEM CELL TRANSPLANT
|
PP-26
|
PINAR
|
CÖMERT
|
AN UNEXPECTED COMPLICATION: TRANSVERSE MYELITIS AFTER
AUTOLOGOUS STEM CELL TRANSPLANTATION
|
PP-27
|
EREN ARSLAN
|
DAVULCU
|
ALLOGENEIC HAEMATOPOIETIC STEM CELL TRANSPLANTATION IN ADULT
APLASTIC ANEMIA PATIENTS
|
PP-28
|
ALİ
|
ÜNAL
|
THE COMPARISON OF MELPHALAN ADMINISTRATION ON DAY–3 WITH
ADMINISTRATION ON DAY –1 ON NEUTROPHIL AND PLATELET ENGRAFTMENT
IN MULTIPLE MYELOMA PATIENTS UNDERGOING AUTOLOGOUS STEM CELL
TRANSPLANTATION
|
PP-29
|
HACER BERNA
|
AFACAN ÖZTÜRK
|
CD81 EXPRESSION IN THE DIFFERENTIAL DIAGNOSIS OF CHRONIC
LYMPHOCYTIC LEUKEMIA
|
PP-30
|
AYSUN
|
SENTURK YIKILMAZ
|
ASSOCIATION OF INITIAL PROGNOSTIC PARAMETERS AND REQUIREMENT
FOR TREATMENT IN CHRONIC LYMPHOCYTIC LEUKEMIA
|
PP-31
|
DAMİRA
|
BAYZAKOVA
|
THE ROLE OF NEW TYROSINE KINASE INHIBITORS IN CHRONIC MYELOID
LEUKEMIA IN KYRGYZSTAN
|
PP-32
|
ALİ
|
DOĞAN
|
A CASE OF MYASTHENIA GRAVIS DEVELOPING FROM CHRONIC MYELOID
LEUKEMIA WITH IMATINIB USE: A CASE REPORT
|
PP-33
|
RAFİYE
|
ÇİFTÇİLER
|
A CASE OF IDIOPATHIC HYPEREOSINOPHILIC SYNDROME WITH HEPATIC
INVOLVEMENT
|