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OUTLINE OF IRON METABOLISM, WITH EMPHASIS TO ERYTHROID CELLS iron Metabolism
2078PDF: 984Html: 344 -
THE HISTORY OF DEFERIPRONE (L1) AND THE COMPLETE TREATMENT OF IRON OVERLOAD IN THALASSAEMIA The history and roles of deferiprone
2444PDF: 1604HTML: 653 -
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ACQUIRED REFRACTORY IRON DEFICIENCY
3439PDF: 1153HTML: 1095 -
MYELODYSPLASTIC SYNDROMES AND IRON CHELATION THERAPY
3413PDF: 1307HTML: 1908Fig.1: 206Fig. 2: 217 -
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
2309PDF: 622Suppl. Files: 286HTML: 178 -
REFRACTORY THROMBOCYTOPENIA AND NEUTROPENIA: A DIAGNOSTIC CHALLENGE
12423PDF: 1687HTML: 4215Cover letter: 205Figure 1: 213 -
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Anemia in the elderly: not always what it seems.
3334PDF: 1081HTML: 1784Figure 1: 186Figure 1 revised: 186 -
NEW TREATMENTS FOR MYELODYSPLASTIC SYNDROMES
2001PDF: 779HTML: 702 -
PROGNOSTIC FACTORS IN HODGKIN LYMPHOMA
3384PDF: 1981HTML: 7482 -
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.
4163PDF: 623HTML: 403 -
IMPORTANCE OF CLASSICAL MORPHOLOGY IN THE DIAGNOSIS OF MYELODYSPLASTIC SYNDROME
3382PDF: 2285HTML: 23363Untitled: 209Untitled: 222Untitled: 239 -
WALDENSTROM’S MACROGLOBULINEMIA: AN UPDATE
7672PDF: 2448HTML: 1742Table 1.: 217Table 2.: 227Table 3.: 211Table 4.: 210 -
VITAMIN D STATUS IN THALASSEMIA MAJOR: AN UPDATE
2760PDF: 1093HTML: 2583 -
HEMOGLOBIN ANALYSIS IN THE FIRST YEAR OF LIFE
3517PDF: 1043HTML: 3054 -
THROMBOCYTOPENIA IN PATIENTS WITH CHRONIC HEPATITIS C VIRUS INFECTION
4158PDF: 1977HTML: 1775 -
miR-155-5p PROMOTES CD34+ APOPTOSIS AND INHIBITS BONE MARROW HEMATOPOIESIS IN MYELODYSPLASTIC SYNDROMES BY RAC1/CREB/MIR-15B AXIS
754PDF: 881PDF Supp. Files: 79HTML: 193 -
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
1213PDF: 957HTML: 461 -
Idiopathic pulmonary embolism in a case of severe family ANKRD26 thrombocytopenia
2165PDF: 845HTML: 932Patient’s family tree: 173
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