Charles A Stanley


Ontology type: schema:Person     


Person Info

NAME

Charles A

SURNAME

Stanley

Publications in SciGraph latest 50 shown

  • 2019-01 Glutamate Dehydrogenase, a Complex Enzyme at a Crucial Metabolic Branch Point in NEUROCHEMICAL RESEARCH
  • 2018 Hypoglycemia in PEDIATRIC ENDOCRINOLOGY
  • 2014-03 Glutamate Dehydrogenase: Structure, Allosteric Regulation, and Role in Insulin Homeostasis in NEUROCHEMICAL RESEARCH
  • 2013-02 The Value of Radiologic Interventions and 18F-DOPA PET in Diagnosing and Localizing Focal Congenital Hyperinsulinism: Systematic Review and Meta-Analysis in MOLECULAR IMAGING AND BIOLOGY
  • 2013 Hypoglycemia in PEDIATRIC ENDOCRINOLOGY
  • 2010-12 Pregnancy in glycogen storage disease type Ib: gestational care and report of first successful deliveries in JOURNAL OF INHERITED METABOLIC DISEASE
  • 2010-09 The hyperinsulinism/hyperammonemia syndrome in REVIEWS IN ENDOCRINE AND METABOLIC DISORDERS
  • 2007-08 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene in NATURE
  • 2007-01 Mechanisms of Disease: advances in diagnosis and treatment of hyperinsulinism in neonates in NATURE REVIEWS ENDOCRINOLOGY
  • 2006 Disorders of Mitochondrial Fatty Acid Oxidation and Related Metabolic Pathways in INBORN METABOLIC DISEASES
  • 2006 Hyperinsulinism of Infancy: Localization of Focal Forms in PEDIATRIC PET IMAGING
  • 2006-01 Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism in MODERN PATHOLOGY
  • 2005-05 Dominantly inherited hyperinsulinaemic hypoglycaemia in JOURNAL OF INHERITED METABOLIC DISEASE
  • 2003-09 Histopathology of Congenital Hyperinsulinism: Retrospective Study with Genotype Correlations in PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
  • 2001-09 Hyperinsulinism and Hyperammonemia Syndrome: Report of Twelve Unrelated Patients in PEDIATRIC RESEARCH
  • 2001-03 Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Clinical Course and Description of Causal Mutations in Two Patients in PEDIATRIC RESEARCH
  • 1999-04 Acute Insulin Response to Leucine: A Diagnostic Tool for the Hyperinsulinism/Hyperammonemia Syndrome in PEDIATRIC RESEARCH
  • 1998-04 “Leucine Sensitive Hypoglycemia” Caused by a Dominantly-inherited Mutation of Glutamate Dehydrogenase • 442 in PEDIATRIC RESEARCH
  • 1998-03 Linkage-disequilibrium mapping without genotyping in NATURE GENETICS
  • 1996-04 USE OF A SENSITIVE ASSAY TO DOCUMENT ELEVATED INSULIN LEVELS IN CONGENITAL HYPERINSULINISM. † 575 in PEDIATRIC RESEARCH
  • 1996-04 HYPERINSULINISM AND HYPERAMMONEMIA: A DISTINCT GENETIC SYNDROME.† 882 in PEDIATRIC RESEARCH
  • 1995-05 Glycine andl-carnitine therapy in 3-methylcrotonyl-CoA carboxylase deficiency in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1994-06 Familial hyperinsulinism maps to chromosome 11p14–15.1, 30 cM centromeric to the insulin gene in NATURE GENETICS
  • 1994-01 In Vitro and In Vivo Effects of Granulocyte Colony-Stimulating Factor on Neutrophils in Glycogen Storage Disease Type IB: Granulocyte Colony-Stimulating Factor Therapy Corrects the Neutropenia and the Defects in Respiratory Burst Activity and Ca2+ Mobilization in PEDIATRIC RESEARCH
  • 1993-09 Interferon-γ Corrects the Respiratory Burst Defect In Vitro in Monocyte-Derived Macrophages from Glycogen Storage Disease Type 1b Patients in PEDIATRIC RESEARCH
  • 1993-07 Renal Handling of Carnitine in Secondary Carnitine Deficiency Disorders in PEDIATRIC RESEARCH
  • 1993-01 Impairment of calcium mobilization in phagocytic cells in glycogen storage disease type 1b in EUROPEAN JOURNAL OF PEDIATRICS
  • 1992-09 Elevated plasma carnitine in the hepatic form of carnitine palmitoyltransferase-1 deficiency in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1989-06 Medium-chain acyl-CoA dehydrogenase deficiency: Metabolic effects and therapeutic efficacy of long-terml-carnitine supplementation in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1989-06 Hyperfiltration and renal disease in glycogen storage disease, type I in KIDNEY INTERNATIONAL
  • 1986-05 Impaired Chemotaxis and Neutrophil (Polymorphonuclear Leukocyte) Function in Glycogenosis Type IB in PEDIATRIC RESEARCH
  • 1985-07 Genetic Deficiency of Medium-Chain Acyl Coenzyme A Dehydrogenase: Studies in Cultured Skin Fibroblasts and Peripheral Mononuclear Leukocytes in PEDIATRIC RESEARCH
  • 1985-07 Long-Chain Acyl Coenzyme A Dehydrogenase Deficiency: An Inherited Cause of Nonketotic Hypoglycemia in PEDIATRIC RESEARCH
  • 1984-04 LOW DOSE ENDOTOXIN (EN) AND FIBRONECTIN (FN) DEPLETION IN RATS: A MODEL OF REYE'S SYNDROME in PEDIATRIC RESEARCH
  • 1984-04 EFFECTS OF VALPROIC ACID (DEPAKENE) ON KETOGENESIS (K), GLUCONEOGENESIS (G), AND UREAGENESIS (U) BY RAT HEPATOCYTES in PEDIATRIC RESEARCH
  • 1984-04 URINE CARNITINE EXCRETION IN SECONDARY CARNITINE DEFICIENCY in PEDIATRIC RESEARCH
  • 1983-11 Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Children with Non-Ketotic Hypoglycemia and Low Carnitine Levels in PEDIATRIC RESEARCH
  • 1983-03 Development of Hepatic Fatty Acid Oxidation and Ketogenesis in the Newborn Guinea Pig in PEDIATRIC RESEARCH
  • 1981-12 Intragastric Feeding in Type I Glycogen Storage Disease: Factors Affecting the Control of Lactic Acidemia in PEDIATRIC RESEARCH
  • 1978-04 457 THE EFFECT OF POSTNATAL AGE ON THE METABOLISM OF INTRAVENOUS FAT EMULSION in PEDIATRIC RESEARCH
  • 1978-04 906 EFFECT OF EARLY FEEDING ON PLASMA GLUCOSE IN SMALL-FOR-DATES (SGA) NEONATES in PEDIATRIC RESEARCH
  • 1977-04 THE FED HUMAN NEONATE-A SUCKLING KETOSIS? in PEDIATRIC RESEARCH
  • 1977-04 DEFICIENT KETOGENESIS IN NEONATAL HYPOGLYCEMIA in PEDIATRIC RESEARCH
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