Works by Stanley, Charles A.
Results: 95
Histopathology of Congenital Hyperinsulinism: Retrospective Study with Genotype Correlations.
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- Pediatric & Developmental Pathology, 2003, v. 6, n. 4, p. 322, doi. 10.1007/s10024-002-0026-9
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- Article
Perceptions of NRCS Assistance with Prescribed Fires on U.S. Private Lands: A Regionally Stratified Case Study.
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- Fire (2571-6255), 2021, v. 4, n. 3, p. 1, doi. 10.3390/fire4030047
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- Article
Novel dominant K<sub>ATP</sub> channel mutations in infants with congenital hyperinsulinism: Validation by in vitro expression studies and in vivo carrier phenotyping.
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- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 11, p. 2214, doi. 10.1002/ajmg.a.61335
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- Article
Hyperinsulinemic hypoglycemia in seven patients with de novo NSD1 mutations.
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- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 4, p. 542, doi. 10.1002/ajmg.a.61062
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- Article
Neurological aspects in hyperinsulinism-hyperammonaemia syndrome.
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- Developmental Medicine & Child Neurology, 2008, v. 50, n. 12, p. 888, doi. 10.1111/j.1469-8749.2008.03149.x
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- Article
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.
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- 2007
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- Letter
Eating Disorder or Disordered Eating; an Interesting Case Study.
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- 2024
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- Abstract
The value of radiologic interventions and (18)F-DOPA PET in diagnosing and localizing focal congenital hyperinsulinism: systematic review and meta-analysis.
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- 2013
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- journal article
The Value of Radiologic Interventions and F-DOPA PET in Diagnosing and Localizing Focal Congenital Hyperinsulinism: Systematic Review and Meta-Analysis.
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- Molecular Imaging & Biology, 2013, v. 15, n. 1, p. 97, doi. 10.1007/s11307-012-0572-0
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- Article
CAUSES OF IN-FACEPIECE SAMPLING BIAS—I. HALF-FACEPIECE RESPIRATORS*.
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- Annals of Occupational Hygiene, 1988, v. 32, n. 3, p. 345
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- Article
Ethical Attitudes of Accountants: Recent Evidence from a Practitioners’ Survey.
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- Journal of Business Ethics, 2007, v. 71, n. 1, p. 73, doi. 10.1007/s10551-006-9125-2
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- Article
A Comparative Account of the Development of the Heart of a Newt and a Frog.
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- Acta Zoologica, 1967, v. 48, p. 43, doi. 10.1111/j.1463-6395.1967.tb00131.x
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- Article
A novel atypical presentation of insulin autoimmune syndrome (Hirata's disease) in a child.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 11/12, p. 1163, doi. 10.1515/jpem-2013-0215
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- Article
Glutamate Dehydrogenase, a Complex Enzyme at a Crucial Metabolic Branch Point.
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- Neurochemical Research, 2019, v. 44, n. 1, p. 117, doi. 10.1007/s11064-017-2428-0
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- Article
Glutamate Dehydrogenase: Structure, Allosteric Regulation, and Role in Insulin Homeostasis.
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- Neurochemical Research, 2014, v. 39, n. 3, p. 433, doi. 10.1007/s11064-013-1173-2
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- Article
Novel Hypoglycemia Phenotype in Congenital Hyperinsulinism Due to Dominant Mutations of Uncoupling Protein 2.
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- 2016
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- journal article
Perspective on the Genetics and Diagnosis of Congenital Hyperinsulinism Disorders.
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- 2016
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- journal article
Histologic and Molecular Profile of Pediatric Insulinomas: Evidence of a Paternal Parent-of-Origin Effect.
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- 2016
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- journal article
High Risk of Diabetes and Neurobehavioral Deficits in Individuals With Surgically Treated Hyperinsulinism.
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- 2015
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- journal article
Novel presentations of congenital hyperinsulinism due to mutations in the MODY genes: HNF1A and HNF4A.
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- 2012
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- journal article
Nesidioblastosis No Longer! It’s All about Genetics.
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- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 3, p. 617, doi. 10.1210/jc.2011-0164
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- Article
The Diagnosis of Ectopic Focal Hyperinsulinism of Infancy with [<sup>18</sup>F]-Dopa Positron Emission Tomography.
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- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 8, p. 2839, doi. 10.1210/jc.2006-0455
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- Article
Genotype-phenotype correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genes.
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- 2005
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- journal article
Familial leucine-sensitive hypoglycemia of infancy due to a dominant mutation of the beta-cell sulfonylurea receptor.
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- 2004
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- journal article
Acute Insulin Responses to Calcium and Tolbutamide Do Not Differentiate Focal from Diffuse Congenital Hyperinsulinism.
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- Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 2, p. 925, doi. 10.1210/jc.2003-030941
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- Article
Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulation.
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- 2004
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- journal article
Editorial: Advances in Diagnosis and Treatment of Hyperinsulinism in Infants and Children.
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- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 11, p. 4857, doi. 10.1210/jc.2002-021403
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- Article
Hyperinsulinism/Hyperammonemia Syndrome in Children with Regulatory Mutations in the Inhibitory Guanosine Triphosphate-Binding Domain of Glutamate Dehydrogenase.
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- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 4, p. 1782, doi. 10.1210/jcem.86.4.7414
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- Article
Suppression of insulin oversecretion by subcutaneous recombinant human insulin-like growth factor I in children with congenital hyperinsulinism due to defective β-cell sulfonylurea receptor.
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- 1999
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- journal article
Dual Regulation of Insulin-Like Growth Factor Binding Protein-1 Levels by Insulin and Cortisol during Fasting.
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- Journal of Clinical Endocrinology & Metabolism, 1998, v. 83, n. 12, p. 4426, doi. 10.1210/jcem.83.12.5347
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- Article
Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinism.
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- Human Mutation, 1999, v. 14, n. 1, p. 23, doi. 10.1002/(SICI)1098-1004(1999)14:1<23::AID-HUMU3>3.0.CO;2-#
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- Article
Hyperfiltration and renal disease in glycogen storage disease, type I.
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- Kidney International, 1989, v. 35, n. 6, p. 1345, doi. 10.1038/ki.1989.133
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- Article
Localized islet nuclear enlargement hyperinsulinism (LINE-HI) due to ABCC8 and GCK mosaic mutations.
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- European Journal of Endocrinology, 2022, v. 187, n. 2, p. 301, doi. 10.1530/EJE-21-1095
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- Article
Extremes of Clinical and Enzymatic Phenotypes in Children With Hyperinsulinism Caused by Glucokinase Activating Mutations.
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- Diabetes, 2009, v. 58, n. 6, p. 1419, doi. 10.2337/db08-1792
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- Article
Congenital hyperinsulinism associated ABCC8 mutations that cause defective trafficking of ATP-sensitive K+ channels: identification and rescue.
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- 2007
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- journal article
Congenital Hyperinsulinism-Associated ABCC8 Mutations That Cause Defective Trafficking of ATP-Sensitive K<sup>+</sup> Channels.
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- Diabetes, 2007, v. 56, n. 9, p. 2339, doi. 10.2337/db07-0150
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- Article
Chronic Elevation of IntraceHular Calcium Impairs the GABA Shunt in Pancreatic Islets of SUR1 Knockout Mice -- Studies with U-13C-Glucose.
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- Diabetes, 2007, v. 56, p. A439
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- Article
The Role of Glutamine-Glutamate-a-Ketoglutarate Axis in Amino Acid Stimulated Insulin Secretion in the beta-HC9 Cells.
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- Diabetes, 2007, v. 56, p. A435
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- Article
Two K[sub ATP] Channel Mutants with Congenital Hyperinsulinism Disease Phenotype Exhibit Diabetes-Inducing Gating Properties.
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- Diabetes, 2007, v. 56, p. A433
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- Article
A Mutation in the TMD0-L0 Region of Sulfonylurea Receptor-1 (L225P) Causes Permanent Neonatal Diabetes Mellitus (PNDM).
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- Diabetes, 2007, v. 56, n. 5, p. 1357, doi. 10.2337/db06-1746
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- Article
From Clinicogenetic Studies of Maturity-Onset Diabetes of the Young to Unraveling Complex Mechanisms of Glucokinase Regulation.
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- Diabetes, 2006, v. 55, n. 6, p. 1713, doi. 10.2337/db05-1513
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- Article
Clinical and molecular characterization of a dominant form of congenital hyperinsulinism caused by a mutation in the high-affinity sulfonylurea receptor.
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- 2003
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- journal article
Glutaminolysis and insulin secretion: from bedside to bench and back.
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- 2002
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- journal article
Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations.
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- 2001
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- journal article
Molecular basis and characterization of the hyperinsulinism/hyperammonemia syndrome: predominance of mutations in exons 11 and 12 of the glutamate dehydrogenase gene. HI/HA Contributing Investigators.
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- 2000
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- journal article
Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.
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- 1999
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- journal article
A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism.
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- 1997
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- Publication type:
- journal article
Case presentation of 8-year follow up of recurrent malignant duodenal Insulinoma and lymph node metastases and literature review of malignant Insulinoma management.
- Published in:
- BMC Endocrine Disorders, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12902-022-01219-9
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- Article
Ethics in the Accounting Profession and the Brazilian "Jeitinho": a Profile Analysis of Accounting Students in Brazil.
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- Pensar Contábil, 2020, v. 22, n. 77, p. 45
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- Article
PET/MR Imaging Consensus Paper: A Joint Paper by the Society of Nuclear Medicine and Molecular Imaging Technologist Section and the Section for Magnetic Resonance Technologists.
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- Journal of Nuclear Medicine Technology, 2013, v. 41, n. 2, p. 108, doi. 10.2967/jnmt.113.123869
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- Article