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OUTLINE OF IRON METABOLISM, WITH EMPHASIS TO ERYTHROID CELLS iron Metabolism
2405PDF: 1211Html: 969 -
THE HISTORY OF DEFERIPRONE (L1) AND THE COMPLETE TREATMENT OF IRON OVERLOAD IN THALASSAEMIA The history and roles of deferiprone
2512PDF: 1640HTML: 706 -
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ACQUIRED REFRACTORY IRON DEFICIENCY
3687PDF: 1266HTML: 1457 -
MYELODYSPLASTIC SYNDROMES AND IRON CHELATION THERAPY
3780PDF: 1341HTML: 2168Fig.1: 238Fig. 2: 232 -
JUSTIFICATION OF UNIVERSAL IRON SUPPLEMENTATION FOR INFANTS 6-12 MONTHS IN REGIONS WITH A HIGH PREVALENCE OF THALASSEMIA Iron Supplementation for Infants 6-12 months in Regions with a High Prevalence of Thalassemia
3308PDF: 646Suppl. Files: 304HTML: 277 -
REFRACTORY THROMBOCYTOPENIA AND NEUTROPENIA: A DIAGNOSTIC CHALLENGE
12956PDF: 1734HTML: 4351Cover letter: 225Figure 1: 234 -
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Anemia in the elderly: not always what it seems.
3396PDF: 1120HTML: 1803Figure 1: 211Figure 1 revised: 208 -
NEW TREATMENTS FOR MYELODYSPLASTIC SYNDROMES
2088PDF: 1624HTML: 804 -
PROGNOSTIC FACTORS IN HODGKIN LYMPHOMA
3459PDF: 2045HTML: 7575 -
THE HEMATOLOGICAL PARAMETERS AND BIOCHEMICAL MARKERS OF IRON STATUS IN ALFA-THALASSEMIA 3.7KB DELETION FROM METROPOLITAN REGION OF MANAUS, AMAZONAS, BRAZIL. alfa-Thalassemia 3.7 deletion From Amazonas, Brazil.
4239PDF: 671HTML: 467 -
IMPORTANCE OF CLASSICAL MORPHOLOGY IN THE DIAGNOSIS OF MYELODYSPLASTIC SYNDROME
3535PDF: 2320HTML: 23499Untitled: 234Untitled: 245Untitled: 252 -
WALDENSTROM’S MACROGLOBULINEMIA: AN UPDATE
7878PDF: 2492HTML: 2119Table 1.: 249Table 2.: 259Table 3.: 241Table 4.: 236 -
VITAMIN D STATUS IN THALASSEMIA MAJOR: AN UPDATE
2841PDF: 1123HTML: 2628 -
HEMOGLOBIN ANALYSIS IN THE FIRST YEAR OF LIFE
3630PDF: 1082HTML: 3079 -
miR-155-5p PROMOTES CD34+ APOPTOSIS AND INHIBITS BONE MARROW HEMATOPOIESIS IN MYELODYSPLASTIC SYNDROMES BY RAC1/CREB/MIR-15B AXIS
804PDF: 921PDF Supp. Files: 91HTML: 254 -
THROMBOCYTOPENIA IN PATIENTS WITH CHRONIC HEPATITIS C VIRUS INFECTION
4306PDF: 2027HTML: 1958 -
HEMATOPOIETIC STEM CELL TRANSPLANTATION IN SEVERE PEDIATRIC SICKLE CELL DISEASE: OUTCOME AND LONG-TERM COMPLICATIONS, SAUDI EXPERIENCE AT KING FAISAL SPECIALIST HOSPITAL, RIYADH, SAUDI ARABIA HCT in in Severe Pediatric Sickle Cell Disease
1395PDF: 1008HTML: 498 -
Idiopathic pulmonary embolism in a case of severe family ANKRD26 thrombocytopenia
2339PDF: 874HTML: 969Patient’s family tree: 202
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