20 results on '"Gangarossa, Simone"'
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2. Becker’s Nevus Syndrome (Pigmentary Hairy Epidermal Nevus)
3. MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness
4. Immunocytochemistry for the heavy chain of the non-muscle myosin IIA as a diagnostic tool for MYH9-related disorders
5. Genetics, clinical and pathological features of glomerulonephrites associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)
6. Acute myeloid leukemia in a twin with a suprasellar arachnoid cyst: a possible correlation
7. Low serum levels of interleukin-6 in children with post-infective acute thrombocytopenic purpura
8. Iron status in white sickle cell disease patients
9. Dissecting clinical findings: platelet defects segregate independently of deafness and cataract in a family affected by an apparent syndromic form of macrothrombocytopenia
10. MYH9-Related Disease
11. Micromegakaryocytes in a patient with partial deletion of the long arm of chromosome 11 [del(11)(q24.2qter)] and chronic thrombocytopenic purpura
12. Efficacy of Oral Administration of High-Dose Cobamamide in a Patient with Imerslund-Grasbeck Syndrome
13. Congenital Dyserythropoietic Anemia Type II Associated with G6PD Seattle in a Sicilian Child
14. High-Dose Intravenous Immunoglobulin Therapy, Blood Rheology, and Sickle Cell Anemia
15. Desferrioxamine in the treatment of plasmodium falciparum malaria
16. Interleukin-6 and Thrombocytopoiesis: Probable Role of Platelets During Acute Phase Responses
17. Prenatal Diagnosis of Cloacal Anomaly.
18. Low serum levels of interleukin-6 in children with post-infective acute thrombocytopenic purpura.
19. Iron status in white sickle cell disease patients.
20. Dysmegakaryopoietic Thrombocytopenia in Patients With Distal Chromosome 11q Deletion
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