Associate Professor, Pediatrics, Perelman School of Medicine
Pediatric Hematology & Oncology
Dr. Janet L. Kwiatkowski, MD
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Janet Kwiatkowski practices Pediatric Hematology & Oncology. She graduated from Columbia University College of Physicians & Surgeons. Columbia University College of Physicians & Surgeons is one of the top medical schools in the US. Columbia University College of Physicians & Surgeons is ranked 8 in research and 52 in primary care medicine She received awards:"Super Doctor". Janet Kwiatkowski is also published. She has 63 publications published. The lastest publication: "Schwann cell-conditioned medium promotes neuroblastoma survival and differentiation.'
Publications
- Effects of hydroxyurea treatment for patients with hemoglobin SC Disease.
- Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with Sickle cell anaemia-TCD With Transfusions Changing...
- Increasing prevalence of Thalassemia in America: Implications for primary care.
- Intracranial aneurysms in sickle cell Anemia: clinical and imaging findings.
- Therapeutic phlebotomy is safe in children with Sickle cell anaemia and can be effective treatment for transfusional iron overload.
- Controlled trial of transfusions for silent cerebral infarcts in sickle cell Anemia.
- Variance of pain prevalence and associated severity during the transfusion cycle of adult thalassaemia patients.
- Sickle cell Anemia: Intracranial stenosis and silent cerebral infarcts in children with low risk of stroke.
- Headache and Migraine in Children with Sickle Cell Disease Are Associated with Lower Hemoglobin and Higher Pain Event Rates But Not Silent Cerebral Infarction.
- Evaluation and treatment of transfusional iron overload in children.
- Prevalence of intracranial stenosis and silent cerebral infarcts in children with sickle cell Anemia and low risk of stroke.
- Pregnancy outcomes in women with Thalassemia in North America and the United Kingdom.
- Zinc supplementation improves bone density in patients with Thalassemia: a double-blind, randomized, placebo-controlled trial.
- Increased leucocyte apoptosis in transfused ?-thalassaemia patients.
- Sickle cell disease in children: accuracy of imaging transcranial Doppler ultrasonography in detection of intracranial arterial stenosis.
- Risks factors and mortality associated with an elevated tricuspid-regurgitant-jet-velocity measured by Doppler-echocardiography in Thalassemia: a Thalassemia Clinical ...
- Characterization of low bone mass in young patients with Thalassemia by DXA, pQCT and markers of bone turnover.
- Central Nervous System Events in Children with Sickle Cell Disease Presenting Acutely with Headache.
- Real-world use of iron chelators.
- Sickle cell disease and transcranial Doppler imaging: inter-hemispheric differences in blood flow Doppler parameters.
- Education and employment status of children and adults with Thalassemia in North America.
- Transcranial Doppler ultrasonography and prophylactic transfusion program is effective in preventing overt stroke in children with Sickle cell disease.
- Transcranial Doppler ultrasonography in infants with Sickle cell disease-Is earlier identification of children at risk of stroke possible?
- Oral iron chelators.
- Serum ferritin level changes in children with Sickle cell disease on chronic blood transfusion are nonlinear and are associated with iron load and liver injury.
- Sickle cell disease: ratio of blood flow velocity of intracranial to extracranial cerebral arteries--initial experience.
- Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function.
- Headache in children with Sickle cell disease: prevalence and associated factors.
- Prolongation of the prothrombin time and activated partial thromboplastin time in children with Sickle cell disease.
- Neutropenia following IVIG therapy in pediatric patients with Immune-mediated thrombocytopenia.
- Iron chelation therapy in sickle-cell disease and other transfusion-dependent Anemias.
- Stroke and elevated blood flow velocity in the anterior cerebral artery in Sickle cell disease.
- Schwann Cell-conditioned medium promotes neuroblastoma survival and differentiation.
- Blood transfusion support in pediatric cardiovascular surgery.
- High-level expression of angiogenic factors is associated with advanced tumor stage in human neuroblastomas.
- Pain as an emergent issue in Thalassemia.
- Sickle cell disease: reference values and interhemispheric differences of nonimaging transcranial Doppler blood flow parameters.
- Relative response of patients with myelodysplastic syndromes and other transfusion-dependent anaemias to deferasirox (ICL670): a 1-yr prospective study.
- Quality of life in Thalassemia: a comparison of SF-36 results from the Thalassemia longitudinal cohort to reported literature and the US norms.
- Severe iron deficiency Anemia in young children.
- A pilot study of subcutaneous decitabine in β-Thalassemia intermedia.
- Iron chelation adherence to deferoxamine and deferasirox in Thalassemia.
- Angle-corrected imaging transcranial doppler sonography versus imaging and nonimaging transcranial doppler sonography in children with Sickle cell disease.
- Prevalence of fractures among the Thalassemia syndromes in North America.
- Epidemiology of human parvovirus B19 in children with Sickle cell disease.
- Transcranial Doppler ultrasonography in siblings with Sickle cell disease.
- Elevated blood flow velocity in the anterior cerebral artery and stroke risk in Sickle cell disease: extended analysis from the STOP trial.
- Chronic transfusion practice for children with Sickle cell anaemia and stroke.
- Safety and efficacy of pegylated interferon alpha-2a and ribavirin for the treatment of hepatitis C in patients with Thalassemia.
- Bone Disease in thalassemia: a frequent and still unresolved problem.
- Inflammation and oxidant-stress in beta-Thalassemia patients treated with iron chelators deferasirox (ICL670) or deferoxamine: an ancillary study of the Novartis CICL6...
- Differences in the prevalence of growth, endocrine and vitamin D abnormalities among the various thalassaemia syndromes in North America.
- Silent infarcts in young children with Sickle cell disease.
- Hemoglobin H-constant spring in North America: an alpha Thalassemia with frequent complications.
- Symptoms of depression and anxiety in patients with Thalassemia: prevalence and correlates in the Thalassemia longitudinal cohort.
- Transfusion and chelation practices in Sickle cell disease: a regional perspective.
- Relationship between chronic transfusion therapy and body composition in subjects with Thalassemia.
- Effect of transfusion therapy on transcranial Doppler ultrasonography velocities in children with Sickle cell disease.
- Renal dysfunction in patients with thalassaemia.
- Red Cell alloimmunization in a diverse population of transfused patients with thalassaemia.
- A phase 1 dose-escalation study: safety, tolerability, and pharmacokinetics of FBS0701, a novel oral iron chelator for the treatment of transfusional iron overload.
- Management of transfusional iron overload - differential properties and efficacy of iron chelating agents.
Schools
Columbia University College Of Physicians and Surgeons
Children39s Hospital Philadelphia
Johns Hopkins University School Med
Procedures Preformed
- Plasmapheresis
Conditions Treated
- Anemia
- Coagulation Disorders (incl. Hemophilia)
- Deep Vein Thrombosis (DVT)
- Hypercoagulable State
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Doctors Specialties
- Pediatric Hematology
- Oncology
Accepted Insurances
Awards
- Super Doctor
Education
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Children's Hospital of Philadelphia -
Johns Hopkins University -
Columbia University College of Physicians & Surgeons
Hospital
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Hospital of the University of Pennsylvania -
Pennsylvania Hospital
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