Physician
Pediatric Hematology & Oncology
Dr. Caterina P. Minniti, MD
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Caterina Minniti works in the field of Pediatric Hematology & Oncology. Caterina Minniti is a published doctor. He has 76 publications published. The most current publication "Carboplatin-induced immune hemolytic anemia."
Publications
- Oscillatory haematopoiesis in adults with sickle cell disease treated with hydroxycarbamide.
- Mutations in TRNT1, encoding the CCA-adding enzyme, cause congenital sideroblastic anemia with B cell immunodeficiency, periodic fevers and developmental delay (SIFD).
- Silent cerebral infarction, income and grade retention among students with sickle cell.
- Activated STING in a Vascular and Pulmonary Syndrome.
- Computed tomography correlates with cardiopulmonary hemodynamics in pulmonary hypertension in adults with sickle cell disease.
- Abnormal pulmonary function and associated risk factors in children and adolescents with sickle cell anemia.
- Efficacy and safety of deferasirox compared with deferoxamine in sickle cell disease: Two-year results including pharmacokinetics and concomitant hydroxyurea.
- A Retrospective Review of Acupuncture Use for the Treatment of Pain in Sickle Cell Disease Patients: Descriptive Analysis From a Single Institution.
- Effect of Extended-Release Niacin on Serum Lipids and on Endothelial Function in Adults With Sickle Cell Anemia and Low High-Density Lipoprotein Cholesterol Levels.
- Vasculopathy, inflammation and blood flow in leg ulcers of patients with sickle cell anemia.
- Liver stiffness increases acutely during sickle cell vaso-occlusive crisis.
- Clinical correlates of acute pulmonary events in children and adolescents with sickle cell disease.
- Leg Ulcers in Sickle Cell Disease: Current Patterns and Practices.
- Genetic determinants of haemolysis in sickle cell anaemia.
- Hemodynamic Predictors of Mortality in Adults with Sickle Cell Disease.
- Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, gender and relative high systolic blood pressure.
- Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemia.
- Anti-haemolytic effect of senicapoc and decrease in NT-proBNP in adults with sickle cell anaemia.
- Predictors of osteoclast activity in sickle cell disease patients.
- Laboratory and echocardiography markers in sickle cell patients with leg ulcers.
- Leg ulcers in sickle cell disease.
- Relationship of erythropoietin, fetal hemoglobin, and hydroxyurea treatment to tricuspid regurgitation velocity in children with sickle cell disease.
- Mediastinal Kaposiform hemangioendothelioma and Kasabach-Merritt phenomenon in an infant: treatment with interferon.
- Transition of patients with sickle cell disease from pediatric to adult care: Assessing patient readiness.
- Reversible posterior leuko-encephalopathy in children with sickle cell disease.
- Angiogenic and inflammatory markers of cardiopulmonary changes in children and adolescents with sickle cell disease.
- Severe vaso-occlusive episodes associated with use of systemic corticosteroids in patients with sickle cell disease.
- Sudden-onset blindness in sickle cell disease due to retinal artery occlusion.
- Pharmacogenetics of morphine: Potential implications in sickle cell disease.
- Utility of PET scans to predict disease relapse in pediatric patients with Hodgkin lymphoma.
- Hydroxyurea therapy lowers TCD velocities in children with sickle cell disease.
- Antibiotic prophylaxis for children with sickle cell disease: a survey of pediatric dentistry residency program directors and pediatric hematologists.
- Transcranial Doppler changes in children with sickle cell disease on transfusion therapy.
- Pseudotumor cerebri in children with sickle cell disease: a case series.
- Hydroxyurea-Increased Fetal Hemoglobin Is Associated with Less Organ Damage and Longer Survival in Adults with Sickle Cell Anemia.
- Hydroxycarbamide in very young children with sickle-cell anaemia: a multicentre, randomised, controlled trial (BABY HUG).
- Opioid patient controlled analgesia use during the initial experience with the IMPROVE PCA trial: a phase III analgesic trial for hospitalized sickle cell patients wit...
- Elevated tricuspid regurgitation velocity and decline in exercise capacity over 22 months of follow up in children and adolescents with sickle cell anemia.
- Endothelin receptor antagonists for pulmonary hypertension in adult patients with sickle cell disease.
- Perioperative management for orthopaedic patients with sickle cell anaemia.
- Design of the silent cerebral infarct transfusion (SIT) trial.
- Segmentation and quantification of pulmonary artery for noninvasive CT assessment of sickle cell secondary pulmonary hypertension.
- Association of G6PD with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia.
- Prospective evaluation of haemoglobin oxygen saturation at rest and after exercise in paediatric sickle cell disease patients.
- Prospective echocardiography assessment of pulmonary hypertension and its potential etiologies in children with sickle cell disease.
- Improvement in hemolysis and pulmonary arterial systolic pressure in adult patients with sickle cell disease during treatment with hydroxyurea.
- rs660 polymorphism in Ro52 (SSA1; TRIM21) is a marker for age-dependent tolerance induction and efficiency of alloimmunization in sickle cell disease.
- Elevated tricuspid regurgitant jet velocity in children and adolescents with sickle cell disease: association with hemolysis and hemoglobin oxygen desaturation.
- Histiocytic sarcoma after acute lymphoblastic leukaemia: a common clonal origin.
- Acute lymphoblastic leukemia in a child with nephrotic syndrome.
- IGF-II in the pathogenesis of rhabdomyosarcoma: a prototype of IGFs involvement in human tumorigenesis.
- Insulin-like growth factor II overexpression in myoblasts induces phenotypic changes typical of the malignant phenotype.
- Specific expression of insulin-like growth factor-II in rhabdomyosarcoma tumor cells.
- Suramin inhibits the growth of human rhabdomyosarcoma by interrupting the insulin-like growth factor II autocrine growth loop.
- The insulin-like growth factor II (IGF-II)/mannose 6-phosphate receptor mediates IGF-II-induced motility in human rhabdomyosarcoma cells.
- Elimination of clonogenic malignant human T cells using monoclonal antibodies in combination with 2'-deoxycoformycin.
- Cranial irradiation and platelet monoamine oxidase in ALL.
- Children's National Medical Center's transfusion protocol for sickle hemoglobinopathies.
- Signals transduced via insulin-like growth factor I receptor (IGF(R)) mediate resistance to retinoic acid-induced cell growth arrest in a human neuroblastoma cell line.
- Giant mucinous cystadenoma in a young patient. A case report.
- [Closed trauma of the spleen. Indications to surgical treatment].
- [Hepatic hydatidosis: old and actual therapeutic strategies].
- [Behavior of lymphocyte subpopulations in acute lymphoblastic leukemia in children].
- Lymphocyte changes in favism: in vitro evidence of a modifying effect of bilirubin and hemoglobin on T-lymphocyte receptors.
- Hysteroscopic retrieval of occult IUD.
- B-cell acute lymphoblastic leukemia and isochromosome 7q.
- Clopidogrel inhibits the binding of ADP analogues to the receptor mediating inhibition of platelet adenylate cyclase.
- Insulin-like growth factor II acts as an autocrine growth and motility factor in human rhabdomyosarcoma tumors.
- T-lymphocyte subpopulation changes during hemolysis in glucose-6-phosphate dehydrogenase (G6PD)-deficient children.
- Phase I trial of etoposide, doxorubicin and cisplatin (EAP) in combination with GM-CSF.
- Carboplatin-induced immune hemolytic anemia.
- [Spontaneous splenic rupture in a patient with cytomegalovirus infection].
- Nosocomial infections in colo-rectal surgery of the old patient.
- Elevated Transpulmonary Gradient and Cardiac Magnetic Resonance-Derived Right Ventricular Remodeling Predict Poor Outcomes in Sickle Cell Disease.
- Osteonecrosis of the Hip in Hematologic Disease: A Review of Conditions and Treatment Options.
Schools
University of Catania Faculty of Medicine And Surgery
University MD School Med
Johns Hopkins University
Nci
Doctors Specialties
- Pediatric Hematology
- Oncology
Accepted Insurances
- Southern Health PPO
- First Health (Coventry Health Care) PPO
Education
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Johns Hopkins University -
University of Maryland -
University of Catania Faculty of Medicine
Hospital
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Montefiore Medical Center
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