Physician
Pediatric Endocrinology
Dr. Paul S. Thornton, MD
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Doctor Paul S. Thornton, MD works in the field of Pediatric Endocrinology. He received awards:"Regional Top Doctor", "Top MD" and "Super Doctor". Paul Thornton is also published. He has 39 publications published. The lastest publication: "Clinical and molecular heterogeneity of familial hyperinsulinism.'
Publications
- Research initiatives in neonatal Hypoglycemia.
- Clinical features and insulin regulation in infants with a Syndrome of prolonged neonatal hyperinsulinism.
- Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism.
- Effects of hypoglycemia on developmental outcome in children With congenital hyperinsulinism.
- GenoType-phenoType correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genes.
- Congenital hyperinsulinism: intraoperative biopsy interpretation can direct the extent of pancreatectomy.
- A multidisciplinary approach to the focal form of congenital hyperinsulinism leads to successful treatment by partial pancreatectomy.
- Preoperative evaluation of infants With focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calci...
- Clinical and molecular characterization of a dominant form of congenital hyperinsulinism caused by a mutation in the high-affinity sulfonylurea receptor.
- Complete androgen insensitivity Syndrome due to X chromosome inversion: a clinical report.
- Histopathology of congenital hyperinsulinism: retrospective study with genoType correlations.
- Reconciling Diabetes management and the ketogenic diet in a child with pyruvate dehydrogenase deficiency.
- Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia Syndrome.
- Dysregulation of insulin secretion in children With congenital hyperinsulinism due to sulfonylurea receptor mutations.
- Acute insulin responses to leucine in children with the hyperinsulinism/hyperammonemia Syndrome.
- Familial and sporadic hyperinsulinism: histopathologic findings and segregation analysis support a single autosomal recessive disorder.
- Short- and long-term use of octreotide in the treatment of congenital hyperinsulinism.
- Insulin-like Growth factor binding protein-1 levels in the diagnosis of hypoglycemia caused by hyperinsulinism.
- A Syndrome of congenital hyperinsulinism and hyperammonemia.
- Familial hyperinsulinism With apparent autosomal dominant inheritance: clinical and genetic differences from the autosomal recessive variant.
- Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.
- A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated With familial hyperinsulinism.
- Management of hyperinsulinism in infants.
- Clinical and molecular heterogeneity of familial hyperinsulinism.
- Mutations in the sulonylurea receptor gene are associated With familial hyperinsulinism in Ashkenazi Jews.
- Intragenic single nucleotide polymorphism haploType analysis of SUR1 mutations in familial hyperinsulinism.
- Familial hyperinsulinism maps to chromosome 11p14-15.1, 30 cM centromeric to the insulin gene.
- Severe transient neonatal hyperinsulinism associated With hyperlactataemia in non-asphyxiated infants.
- Familial hyperinsulinism caused by an activating glucokinase mutation.
- In vitro and in vivo effects of granulocyte colony-stimulating factor on neutrophils in glycogen storage disease Type 1B: granulocyte colony-stimulating factor therapy...
- Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews.
- Genetic heterogeneity in familial hyperinsulinism.
- Hyperinsulinism: molecular aetiology of focal Disease.
- The new highly sensitive adrenocorticotropin assay improves detection of patients With partial adrenocorticotropin deficiency in a short-term metyrapone test.
- p57(KIP2) expression in normal islet cells and in hyperinsulinism of infancy.
- Beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy.
- Growth in children after bone marrow transplantation for acute myelogenous leukemia as compared to acute lymphocytic leukemia.
- A 14-year old girl With reversible hypoglycemic episodes: the role of ASVS.
Schools
Trinity College University Of Dublin University Of Dublin School Of Medicine
Childrens Hospital
Procedures Preformed
- Continuous Glucose Monitoring
Conditions Treated
- Abnormal Thyroid
- Adrenal Insufficiency
- Adrenogenital Disorders
- Calcium Metabolism Disorders
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Doctors Specialties
- Pediatric Endocrinology
Accepted Insurances
- Aetna HMO
- Choice Plus POS II
- Blue Card PPO
- Blue Choice
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- LocalPlus
- Open Access Plus
- First Health (Coventry Health Care) PPO
- Choice Care PPO
- Preferred PPO
- MultiPlan PPO
- PHCS Network PPO
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
Awards
- Regional Top Doctor
- Top MD
- Super Doctor
Education
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Children's Hospital of Philadelphia -
University College of Dublin National Univ SOM
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