Monogenic hyperinsulinemic hypoglycemia: current insights into the pathogenesis and management

Por Lord, Katherine, De León, Diva D
Publicado em 2013

Determination of Insulin for the Diagnosis of Hyperinsulinemic Hypoglycemia

Por De León, Diva D., Stanley, Charles A.
Publicado em 2013

A novel mutation in GATA6 causes pancreatic agenesis

Por Stanescu, Diana E., Hughes, Nkecha, Patel, Puja, De León, Diva D.
Publicado em 2014

Postprandial Hypoglycemia in Children after Gastric Surgery: clinical characterization and pathophysiology

Por Calabria, Andrew C., Charles, Lawrenshey, Givler, Stephanie, De León, Diva D.
Publicado no Horm Res Paediatr (2015)

A novel atypical presentation of insulin autoimmune syndrome (Hirata's disease) in a child

Por Alves, Cresio, Constança, Julia, De León, Diva D., Snider, Kara, Stanley, Charles
Publicado no J Pediatr Endocrinol Metab (2013)

Adding glucagon stimulated GH testing to the diagnostic fast increases the detection of GH sufficient children

Por Hawkes, Colin P, Grimberg, Adda, Dzata, Vivian E, De Leon, Diva D
Publicado no Horm Res Paediatr (2016)

Octreotide use and safety in infants with hyperinsulinism

Por McMahon, Ann W., Wharton, Gerold T., Thornton, Paul, De Leon, Diva D.
Publicado no Pharmacoepidemiol Drug Saf (2016)

A liquid chromatography-mass spectrometry assay for quantification of Exendin[9-39] in human plasma

Por Lasaosa, Maria, Patel, Puja, Givler, Stephanie, De León, Diva D., Seeholzer, Steven H.
Publicado no J Chromatogr B Analyt Technol Biomed Life Sci (2013)

Late presentation of fulminant necrotizing enterocolitis in a child with hyperinsulinism on octreotide therapy

Por Hawkes, Colin Patrick, Adzick, N Scott, Palladino, Andrew A, De León, Diva D
Publicado no Horm Res Paediatr (2016)

Novel Presentations of Congenital Hyperinsulinism due to Mutations in the MODY genes: HNF1A and HNF4A

Por Stanescu, Diana E., Hughes, Nkecha, Kaplan, Bernard, Stanley, Charles A., De León, Diva D.
Publicado em 2012

Clinical Presentation and Management of Children With Diffuse and Focal Hyperinsulinism: A Review of 223 Cases

Por Lord, Katherine, Dzata, Enyo, Snider, Kara E., Gallagher, Paul R., De León, Diva D.
Publicado em 2013

Postoperative Surveillance and Detection of Postprandial Hypoglycemia after Fundoplasty in Children

Por Calabria, Andrew C., Gallagher, Paul R., Simmons, Rebecca, Blinman, Thane, De León, Diva D.
Publicado no J Pediatr (2011)

GLP-1 Receptor Antagonist Exendin-(9-39) Elevates Fasting Blood Glucose Levels in Congenital Hyperinsulinism Owing to Inactivating Mutations in the ATP-Sensitive K(+) Channel

Por Calabria, Andrew C., Li, Changhong, Gallagher, Paul R., Stanley, Charles A., De León, Diva D.
Publicado em 2012

Increased Glucagon-Like Peptide-1 Secretion and Postprandial Hypoglycemia in Children after Nissen Fundoplication

Por Palladino, Andrew A., Sayed, Samir, Levitt Katz, Lorraine E., Gallagher, Paul R., De León, Diva D.
Publicado em 2009

Compound heterozygous mutations in the SUR1 (ABCC 8) subunit of pancreatic K(ATP) channels cause neonatal diabetes by perturbing the coupling between Kir6.2 and SUR1 subunits

Por Lin, Yu-Wen, Akrouh, Alejandro, Hsu, YeouChing, Hughes, Nkecha, Nichols, Colin G., De León, Diva D.
Publicado em 2012

High Risk of Diabetes and Neurobehavioral Deficits in Individuals With Surgically Treated Hyperinsulinism

Por Lord, Katherine, Radcliffe, Jerilynn, Gallagher, Paul R., Adzick, N. Scott, Stanley, Charles A., De León, Diva D.
Publicado no J Clin Endocrinol Metab (2015)

Exendin-(9–39) Corrects Fasting Hypoglycemia in SUR-1(–/–) Mice by Lowering cAMP in Pancreatic β-Cells and Inhibiting Insulin Secretion

Por De León, Diva D., Li, Changhong, Delson, Madeleine I., Matschinsky, Franz M., Stanley, Charles A., Stoffers, Doris A.
Publicado em 2008

Preexisting pancreatic acinar cells contribute to acinar cell, but not islet β cell, regeneration

Por Desai, Biva M., Oliver-Krasinski, Jennifer, De Leon, Diva D., Farzad, Cyrus, Hong, Nankang, Leach, Steven D., Stoffers, Doris A.
Publicado em 2007

Neonatal Diabetes and Congenital Malabsorptive Diarrhea Attributable to a Novel Mutation in the Human Neurogenin-3 Gene Coding Sequence

Por Pinney, Sara E., Oliver-Krasinski, Jennifer, Ernst, Linda, Hughes, Nkecha, Patel, Puja, Stoffers, Doris A., Russo, Pierre, De León, Diva D.
Publicado em 2011

Pharmacological Correction of Trafficking Defects in ATP-sensitive Potassium Channels Caused by Sulfonylurea Receptor 1 Mutations

Por Martin, Gregory M., Rex, Emily A., Devaraneni, Prasanna, Denton, Jerod S., Boodhansingh, Kara E., DeLeon, Diva D., Stanley, Charles A., Shyng, Show-Ling
Publicado no J Biol Chem (2016)