Associate Professor, Pediatrics, University of Tennessee Health Science Center College of Medicine
Pediatric Hematology & Oncology
Dr. Jane S. Hankins, MD
|
|
Give Review
Dr. Jane S. Hankins practices Pediatric Hematology & Oncology. She went to medical school at Federal University of Rio Grande do Sul School of Medicine. Jane S. Hankins, MD is also a published physician. She has 61 publication published. The most recent publication is: Addressing challenges of clinical trials in acute pain: The Pain Management of Vaso-occlusive Crisis in Children and Young Adults with Sickle Cell Disease Study.
Publications
- Paroxysmal cold hemoglobinuria due to an IgA donath-landsteiner antibody.
- The ASPHO 2015 Distinguished Career Award goes to Dr. Winfred C. Wang, MD.
- From infancy to adolescence: fifteen years of continuous treatment with hydroxyurea in sickle cell Anemia.
- Predictors of splenic function preservation in children with sickle cell Anemia treated with hydroxyurea.
- Improved hydroxyurea effect with the use of text messaging in children with sickle cell Anemia.
- Assessment of Sleep-Related Disorders in Children With Sickle Cell Disease.
- Comparing segmented ASL perfusion of vascular territories using manual versus semiautomated techniques in children with sickle cell Anemia.
- Evaluation of SWI in Children With Sickle Cell Disease.
- Protection from sickle cell retinopathy is Associated with elevated HbF levels and hydroxycarbamide use in children.
- Effects of adenotonsillectomy on polysomnographic parameters in children With sickle cell disease.
- Hydroxyurea treatment decreases glomerular hyperfiltration in children with sickle cell Anemia.
- The clinical and laboratory spectrum of Hb C [?6(A3)Glu?Lys, GAG>AAG] Disease.
- Automated T(2) * measurements using supplementary field mapping to assess cardiac iron content.
- Phenocopy of Warfarin Syndrome in an Infant Born to a Mother With Sickle Cell Anemia and Severe Transfusional Iron Overload.
- Exploring family communication about Sickle cell disease in adolescence.
- Parental stress in families of children With a genetic disorder/disability and the resiliency model of family stress, adjustment, and adaptation.
- Simultaneous field and R???2* mapping to quantify liver iron content using autoregressive moving aVerage modeling.
- Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin.
- Glomerular hyperfiltration and albuminuria in children with sickle cell Anemia.
- Neurocognitive screening With the Brigance preschool screen-II in 3-year-old children With sickle cell disease.
- The diagnostic dilemma of congenital unstable hemoglobinopathies.
- Ventricular diastolic dysfunction in sickle cell Anemia is common but not associated with myocardial iron deposition.
- Toward high quality medical care for Sickle cell disease: are we there yet?
- Comparison of whole liver and small region-of-interest measurements of MRI liver R2* in children With iron overload.
- "It's our job": Qualitative study of family responses to ableism.
- Should my child participate in this research study?
- Patterns of liver iron accumulation in patients With sickle cell disease and thalassemia With iron overload.
- Interactions of the RNA-binding protein Hfq With cspA mRNA, encoding the major cold shock protein.
- Irritable bowel syndrome patients' ideal expectations and recent experiences With healthcare providers: a national survey.
- Exploring parent-sibling communication in families of children With sickle cell disease.
- Substrate binding and active site residues in RNases E and G: role of the 5'-sensor.
- Decision analysis of treatment strategies in children With severe sickle cell disease.
- Sickle-cell disease: an ounce of prevention, a pound of cure.
- Simultaneous acute splenic sequestration and transient aplastic crisis in children With sickle cell disease.
- Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients.
- Microarray analysis of liver gene expression in iron overloaded patients with sickle cell Anemia and beta-thalassemia.
- R2* magnetic resonance imaging of the liver in patients With iron overload.
- Pharmacotherapy in sickle cell disease--State of the art and future prospects.
- The painful face of poverty.
- Arterial spin-labeled perfusion combined with segmentation techniques to evaluate cerebral blood flow in white and gray matter of children with sickle cell Anemia.
- Patient educational media preferences for information about irritable bowel syndrome (IBS).
- Biloma and pneumobilia in Sickle cell disease.
- The natural history of conditional transcranial Doppler flow velocities in children With sickle cell anaemia.
- Chemical and functional analysis of generic hydroxyurea formulations.
- Preservation of spleen and brain function in children with sickle cell Anemia treated with hydroxyurea.
- Phase I study of magnesium pidolate in combination With hydroxycarbamide for children With sickle cell anaemia.
- Preparation of the Escherichia coli RNase E protein and reconstitution of the RNA degradosome.
- What patients know about irritable bowel syndrome (IBS) and what they would like to know. National Survey on Patient Educational Needs in IBS and development and valid...
- Therapy preference and decision-making among patients with severe sickle cell Anemia and their families.
- Role of RNA structure and susceptibility to RNase E in regulation of a cold shock mRNA, cspA mRNA.
- Function of the conserved S1 and KH domains in polynucleotide phosphorylase.
- Long-term hydroxyurea therapy for infants with sickle cell Anemia: the HUSOFT extension study.
- The influence of traumatic lumbar puncture and timing of intrathecal therapy on outcome of pediatric acute lymphoblastic leukemia.
- Chronic transfusion therapy for children With sickle cell disease and recurrent acute chest syndrome.
- Thrombocytosis in an infant With high thrombopoietin concentrations.
- Overexpression and purification of untagged polynucleotide phosphorylases.
- The quaternary structure of RNase G from Escherichia coli.
- Prevalence of vitamin d deficiency in sickle cell disease: a Systematic review.
- Hydroxyurea use and hospitalization trends in a comprehensive pediatric Sickle cell program.
- Addressing challenges of clinical trials in acute pain: The Pain Management of Vaso-occlusive Crisis in Children and Young Adults With Sickle Cell Disease Study.
Schools
University of Tennessee
St Jude Chldns Rsch Hospital
Procedures Preformed
- Plasmapheresis
Conditions Treated
- Anemia
- Brain and Nervous System Cancer (incl. Gliomas, Astrocytoma, Schwannoma, Medulloblastoma, Chordoma)
- Brain Cancer
- Coagulation Disorders (incl. Hemophilia)
- View All
Doctors Specialties
- Pediatric Hematology
- Oncology
Accepted Insurances
Education
-
University of Tennessee -
Federal University of Rio Grande do Sul School of Medicine
Hospital
-
University of Tennessee Medical Center -
Le Bonheur Children's Hospital
Helpful Reviews
Similar Doctors
|
Dr. David R. Goshorn, MD
 This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Alberto Broniscer, MD
This Doctor is OpenDoctor Recommended.
 This doctor has more publications
|
|
|
Dr. Yaser Alsaek, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Judith A. Wilimas, MD
This Doctor is OpenDoctor Recommended.
|
|
Dr. Winfred C. Wang, MD
This Doctor is OpenDoctor Recommended.
This doctor has more publications
|
|
|
Dr. Catherine G. Lam, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Sima Jeha, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Alberto S. Pappo, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Jeffrey E. Rubnitz, MD
This Doctor is OpenDoctor Recommended.
This doctor has more publications
|
|
|
Amar J. Gajjar, MB
This Doctor is OpenDoctor Recommended.
This doctor has more publications
|