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Delivery in asymptomatic Italian woman with SARS-CoV-2 infection. Delivery in asymptomatic woman with SARS-CoV-2 infection
1721PDF: 932HTML: 209 -
HEMOGLOBIN ANALYSIS IN THE FIRST YEAR OF LIFE
3364PDF: 975HTML: 3003 -
Screening and genetic diagnosis of Hemoglobinopathies in Southern and Northern Europe: Two examples
1111PDF: 463HTML: 1142Amato1: 152Figure 2 A: Prospective (grey columns) versus retrospective prevention (black columns) among indigenous couples at risk (left) and immigrant couples (right). Among immigrant couples the prevention it is still largely retrospective, while for Italian coupl: 228jdoe, : 236Figure 2 b: Prospective (grey columns) versus retrospective prevention (black columns) among indigenous couples at risk (left) and immigrant couples (right). Among immigrant couples the prevention it is still largely retrospective, while for Italian coupl: 140 -
TYROSINE KINASE INHIBITORS AND PREGNANCY
3397PDF: 1568HTML: 2660 -
AGE AT DIAGNOSIS OF SICKLE CELL ANAEMIA IN LAGOS, NIGERIA
1905PDF: 845HTML: 1836 -
PREVENTION OF ? THALASSEMIA IN NORTHERN ISRAEL - A COST-BENEFIT ANALYSIS.
2392PDF: 1112HTML: 11770 -
DIAGNOSTIC ACCURACY OF CLINICAL TOOL ‘STOPS’ AND SERUM PROCALCITONIN FOR OPTIMIZING ANTIBIOTIC THERAPY IN NEONATAL SEPSIS STOPS and procalcitonin for optimizing antibiotics in neonatal sepsis
1479PDF: 539HTML: 343 -
DIAGNOSTIC VALUE OF SIMULTANEOUS MEASUREMENT OF PROCALCITONIN, INTERLEUKIN-6 AND HS CRP IN PREDICTION OF EARLY-ONSET NEONATAL SEPSIS
1927PDF: 1167HTML: 1908Untitled: 131TaBles Neinates sepsis: 153 -
Refractory Immune Thrombocytopenic Purpura and Cytomegalovirus Infection: A Call for a Change in the Current Guidelines
4128PDF: 1118HTML: 2115Figure 1: 144 -
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How I treat acute and persistent sickle cell pain
1814PDF: 1075HTML: 455 -
A case of iron deficiency anemia with co-existing Hb Fontainebleau.
1255PDF: 727HTML: 2030Untitled: 276 -
Guest Editor: G. Castaman GENE THERAPY FOR HEMOPHILIA: FACTS AND QUANDARIES IN THE 21ST CENTURY GENE THERAPY FOR HEMOPHILIA
1930PDF: 1799HTML: 324 -
PERIOPERATIVE MANAGEMENT OF SICKLE CELL DISEASE: A NARRATIVE REVIEW
7786PDF: 3160HTML: 1166 -
MODULATING EFFECT OF THE ?158 G? (C?T) XMN-1 POLYMORPHISM IN INDIAN SICKLE CELL PATIENTS
1427PDF: 856HTML: 1396Table: 172 -
How we manage invasive fungal disease in acute myeloid leukemia patients with Glucose 6 Dehydrogenase deficiency
1766PDF: 872HTML: 929Referring article: 713 -
PATHOGENESIS OF MALARIA IN TISSUES AND BLOOD
4298PDF: 1859HTML: 17705 -
CIRCUMCISION IN MALES WITH BLEEDING DISORDERS
1843PDF: 848HTML: 6744Cover letter: 143 -
VIRAL HEPATITIS A TO E IN SOUTH MEDITERRANEAN COUNTRIES
1189PDF: 628HTML: 7699 -
END-OF-LIFE CARE IN SICKLE CELL DISEASE AND TRASFUSION DEPENDEND-β-THALASSEMIA: CLINICAL, PSYCHOLOGICAL, AND ETHICAL CONSIDERATION Challenges in Supportive Care, Equity, and Compassion at End of Life
857PDF: 496Html: 140 -
High level of HBV DNA virus in the breast milk seems not to contraindicate breastfeeding
2078PDF: 790HTML: 930Untitled: 248 -
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ON THE VERSATILITY OF VON WILLEBRAND FACTOR
2720PDF: 1075HTML: 11203 -
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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
1911PDF: 570Suppl. Files: 263HTML: 148







