Professor, Pediatrics, University of Texas Southwestern Medical Center, Southwestern Medical School
Pediatric Endocrinology
Dr. Perrin C. White, MD
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Perrin White works in the field of Pediatric Endocrinology. He graduated from Harvard Medical School. Harvard Medical School is a top medical university. Harvard Medical School is ranked 1/12 in Research/PrimaryCare. He over the years received 2 awards: "Regional Top Doctor" and "Elected Member". Perrin White is a published MD. He has 48 publications published. The most current publication "Prostacyclin regulates bone growth via the Epac/Rap1 pathway."
Publications
- Associations of parent-adolescent relationship quality with type 1 Diabetes management and depressive symptoms in latino and caucasian youth.
- Prostacyclin regulates bone growth via the Epac/Rap1 pathway.
- Individual Differences and Day-to-Day Fluctuations in Perceived Self-Regulation Associated With Daily Adherence in Late Adolescents With Type 1 Diabetes.
- Optimizing Newborn Screening for Congenital Adrenal Hyperplasia.
- Low Morbidity and Mortality in Children with Diabetic Ketoacidosis Treated with Isotonic Fluids.
- Congenital adrenal hyperplasia due to 21 hydroxylase deficiency: from birth to adulthood.
- P53 and Cellular Glucose Uptake.
- Toll-like receptors, the NLRP3 inflammasome, and interleukin-1β in the development and progression of type 1 Diabetes.
- Time to failure of oral therapy in children with type 2 Diabetes: a single center retrospective chart review.
- Transient Neonatal Hypocalcemia: Presentation and Outcomes.
- Vitamin D Deficiency in Obese Children and Its Relationship to Glucose Homeostasis.
- Developmental Trajectories of Metabolic Control among White, Black, and Hispanic Youth with Type 1 Diabetes.
- Preliminary studies related to anti-interleukin-1β therapy in children with newly diagnosed type 1 Diabetes.
- Presentation of Primary Adrenal Insufficiency in Childhood.
- Somatic items in the assessment of depressive symptoms in pediatric patients with Diabetes.
- Congenital adrenal hyperplasia owing to 11?-hydroxylase deficiency.
- Studies on the very large g protein-coupled receptor: from initial discovery to determining its role in sensorineural deafness in higher animals.
- A randomized controlled trial comparing motivational interviewing in education to structured Diabetes education in teens with type 1 Diabetes.
- Minireview: steroidogenic factor 1: its roles in differentiation, development, and disease.
- Sitagliptin treatment of patients with type 2 Diabetes does not affect CD4+ T-cell activation.
- SCF, BDNF, and Gas6 are regulators of growth plate chondrocyte proliferation and differentiation.
- Screening for type 2 Diabetes in obese youth.
- Institution of basal-bolus therapy at diagnosis for children with type 1 Diabetes mellitus.
- Adrenarche.
- Physiological roles of 11 beta-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase.
- Deletion of hexose-6-phosphate dehydrogenase activates the unfolded protein response pathway and induces skeletal myopathy.
- Abnormalities of glucose homeostasis and the hypothalamic-pituitary-adrenal axis in mice lacking hexose-6-phosphate dehydrogenase.
- Gene expression in peripheral blood mononuclear cells from children with Diabetes.
- Insulin-like growth factor-I and fibroblast growth factor, but not growth hormone, affect growth plate chondrocyte proliferation.
- The very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundles.
- Ontogeny of adrenal steroid biosynthesis: why girls will be girls.
- Hexose-6-phosphate dehydrogenase knock-out mice lack 11 beta-hydroxysteroid dehydrogenase type 1-mediated glucocorticoid generation.
- Elevated expression of luteinizing hormone receptor in aldosterone-producing adenomas.
- Association of Lys173Arg polymorphism with CYP11B2 expression in normal adrenal glands and aldosterone-producing adenomas.
- Genotypes at 11beta-hydroxysteroid dehydrogenase type 11B1 and hexose-6-phosphate dehydrogenase loci are not risk factors for apparent cortisone reductase deficiency i...
- Expression profiles for steroidogenic enzymes in adrenocortical disease.
- Depressive symptoms predict hospitalization for adolescents with type 1 Diabetes mellitus.
- Editorial: polymorphisms in CYP11B genes and 11-hydroxylase activity.
- A role for the NGFI-B family in adrenal zonation and adrenocortical disease.
- Loss of the transmembrane and cytoplasmic domains of the very large G-protein-coupled receptor-1 (VLGR1 or Mass1) causes audiogenic seizures in mice.
- The orphan nuclear receptors NURR1 and NGFIB regulate adrenal aldosterone production.
- Mutations in the genes encoding 11beta-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency.
- Aldosterone: direct effects on and production by the heart.
- Role of local 11 beta-hydroxysteroid dehydrogenase type 2 expression in determining the phenotype of adrenal adenomas.
- Role of local 11beta-hydroxysteroid dehydrogenase type 2 (HSD11B2) expression in determining the phenotype of adrenal adenomas.
- Very large G protein-coupled receptor-1, the largest known cell surface protein, is highly expressed in the developing central nervous system.
- The endocrinologist's approach to the intersex patient.
Schools
Harvard Medical School
Johns Hopkins Hospital
New York Hospital
Conditions Treated
- Adrenogenital Disorders
- Diabetes Mellitus, Secondary
- Hypokalemia
- Hypothyroidism
- View All
Doctors Specialties
- Pediatric Endocrinology
Accepted Insurances
Awards
- Regional Top Doctor
- Elected Member
Education
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New York Presbyterian Hospital - Cornell Campus -
Johns Hopkins University -
Harvard Medical School
Hospital
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Children's Health System of Texas -
University of Texas Southwestern Medical Center
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