Search
Search Results
##search.searchResults.foundPlural##
-
GLUCOSE HOMEOSTASIS AND ΑSSESSMENT OF Β-CELL FUNCTION BY 3-HOUR ORAL GLUCOSE TOLERANCE (OGTT) IN PATIENTS WITH Β-THALASSEMIA MAJOR WITH SERUM FERRITIN BELOW 1,000 NG/DL: RESULTS FROM A SINGLE ICET-A CENTRE OGTT in thalassemia and iron overload
4013PDF: 1151HTML: 466 -
Postpandemic influenza A/H1N1pdm09 is still causing severe perinatal complications
1399PDF: 1011HTML: 2034Cover letter: 210 -
BONE MARROW ABONRMALITIES IN HIV INFECTION
1938PDF: 1170HTML: 1777 -
-
Osteolytic bone lesions – A rare presentation of AML M6.
2039PDF: 1143HTML: 7982Untitled: 216 -
COULD PLASMA GLUCOSE (PG) INCREMENT (PG %) EXPAND THE CLINICAL WEIGHT OF OGTT? PRELIMINARY FINDINGS IN 19 TDT PATIENTS (Β-TDT) WITH NORMAL GLUCOSE TOLERANCE Plasma glucose (PG) increment (PG %) and pancretic β-cell dysfunction in thalassemia
774PDF: 645HTML: 125 -
SYSTEMIC MASTOCYTOSIS: MULTIDISCIPLINARY APPROACH Systemic Mastocytosis
1635PDF: 1083HTML: 429 -
FLT3 Mutated Acute Myeloid Leukemia after CD19 CAR-T Cells
1018PDF: 1244HTML: 120 -
MILD BLEEDERS: DIAGNOSIS IS ELUSIVE IN LARGE NUMBER OF PATIENTS
3366PDF: 741HTML: 759Figure 1 Distribution of the various causes of mild bleeding (in %) in males and females: 198Figure 2 Age and Sex distribution of patients with Bleeding disorders- Unclassified: 201Table : Distribution of the sites of bleeding and their causes: 195 -
Severe Acute Hepatitis B Treated with Entecavir
1638PDF: 852HTML: 2536Figure: 185Title page: 183disclosure: 111 -
DETECTION OF ANTINUCLEAR ANTIBODIES TARGETING INTRACELLULAR SIGNAL TRANSDUCTION, METABOLISM, APOPTOTIC PROCESSES AND CELL DEATH IN CRITICAL COVID-19 PATIENTS
1451PDF: 1061HTML: 435Suppl. Figure: 195Suppl. Tables: 216 -
Invasive Pulmonary Aspergillosis in a Sickle Cell Patient Transplant Recipient: A Successful Treatment
1985PDF: 1139HTML: 1922Lung computed tomography CT scan image: 215 -
HEMATOPOIETIC STEM CELL TRNSPLANTATION IN THALASSEMIA AND RELATED DISORDERS
1791PDF: 500HTML: 4033 -
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
1359PDF: 978HTML: 496 -
ACQUIRED REFRACTORY IRON DEFICIENCY
3552PDF: 1237HTML: 1198 -
AUTOIMMUNE CYTOPENIAS IN CHRONIC LYMPHOCYTIC LEUKEMIA, FACTS AND MYTHS
2287PDF: 1228HTML: 3892 -
A MULTICENTER ICET-A STUDY ON AGE AT MENARCHE AND MENSTRUAL CYCLES IN PATIENTS WITH TRANSFUSION-DEPENDENT THALASSEMIA (TDT) WHO STARTED EARLY CHELATION THERAPY WITH DIFFERENT CHELATING AGENTS. Age at menarche and menstrual cycles in patients with transfusion-dependent thalassemia.
837PDF: 557HTML: 130







