Works by Stanley, Charles A.

Results: 98

Nabokov and World Literature.

Published in:

CLCWeb: Comparative Literature & Culture: A Web Journal, 2006, v. 8, n. 2, p. 1, doi. 10.7771/1481-4374.1307

By:

Ross, Charles Stanley

Publication type:

Article

MAKING THE RIGHT CALLS.

Published in:

Strategic Finance, 2016, v. 97, n. 10, p. 32

By:

MACGREGOR, JASON;
STANLEY, CHARLES;
STUEBS, MARTIN

Publication type:

Article

Acute Fatty Liver of Pregnancy, Hemolysis, Elevated Liver Enzymes, and Low Platelets Syndrome, and Long Chain 3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency.

Published in:

American Journal of Gastroenterology (Springer Nature), 1996, v. 91, n. 11, p. 2293

By:

Treem, William R.;
Shoup, Marie E.;
Hale, Daniel E.;
Bennett, Michael J.;
Rinaido, Piero;
Millington, David S.;
Stanley, Charles A.;
Riely, Caroline A.;
Hyams, Jeffrey S.

Publication type:

Article

Decreased KATP Channel Activity Contributes to the Low Glucose Threshold for Insulin Secretion of Rat Neonatal Islets.

Published in:

Endocrinology, 2021, v. 162, n. 9, p. 1, doi. 10.1210/endocr/bqab121

By:

Yang, Juxiang;
Hammoud, Batoul;
Li, Changhong;
Ridler, Abigail;
Yau, Daphne;
Kim, Junil;
Won, Kyoung-Jae;
Stanley, Charles A;
Hoshi, Toshinori;
Stanescu, Diana E

Publication type:

Article

Histopathology of Congenital Hyperinsulinism: Retrospective Study with Genotype Correlations.

Published in:

Pediatric & Developmental Pathology, 2003, v. 6, n. 4, p. 322, doi. 10.1007/s10024-002-0026-9

By:

Suchi, Mariko;
MacMullen, Courtney;
Thornton, Paul S.;
Ganguly, Arupa;
Stanley, Charles A.;
Ruchelli, Eduardo D.

Publication type:

Article

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.

Published in:

2007

By:

Hakonarson, Hakon;
Grant, Struan F. A.;
Bradfield, Jonathan P.;
Marchand, Luc;
Kim, Cecilia E.;
Glessner, Joseph T.;
Grabs, Rosemarie;
Casalunovo, Tracy;
Taback, Shayne P.;
Frackelton, Edward C.;
Lawson, Margaret L.;
Robinson, Luke J.;
Skraban, Robert;
Lu, Yang;
Chiavacci, Rosetta M.;
Stanley, Charles A.;
Kirsch, Susan E.;
Rappaport, Eric F.;
Orange, Jordan S.;
Monos, Dimitri S.

Publication type:

Letter

Endocardial fibroelastosis and primary carnitine deficiency due to a defect in the plasma membrane carnitine transporter.

Published in:

Clinical Cardiology, 1996, v. 19, n. 3, p. 243, doi. 10.1002/clc.4960190320

By:

Bennett, Michael J.;
Hale, Daniel E.;
Pollitt, Rodney J.;
Variend, Sadick;
Stanley, Charles A.

Publication type:

Article

Ethical Attitudes of Accountants: Recent Evidence from a Practitioners’ Survey.

Published in:

Journal of Business Ethics, 2007, v. 71, n. 1, p. 73, doi. 10.1007/s10551-006-9125-2

By:

Emerson, Tisha;
Conroy, Stephen;
Stanley, Charles

Publication type:

Article

EFFECTS OF SILICA EXPOSURE ON SUBSTANCE P IMMUNOREACTIVITY AND PREPROTACHYKININ mRNA EXPRESSION IN TRIGEMINAL SENSORY NEURONS IN FISCHER 344 RATS.

Published in:

Journal of Toxicology & Environmental Health: Part A, 1998, v. 53, n. 8, p. 593, doi. 10.1080/009841098159051

By:

Hunter, Dawn D.;
Castranova, Vincent;
Stanley, Charles;
Dey, Richard D.

Publication type:

Article

Hyperfiltration and renal disease in glycogen storage disease, type I.

Published in:

Kidney International, 1989, v. 35, n. 6, p. 1345, doi. 10.1038/ki.1989.133

By:

Baker, Lester;
Dahlem, Stephen;
Goldfarb, Stanley;
Kern, Elizabeth F. O.;
Stanley, Charles A.;
Egler, Joseph;
Olshan, Jerrold S.;
Heyman, Sidney

Publication type:

Article

Coupling Fish Community Structure with Instream Flow and Habitat Connectivity between Two Hydrologically Extreme Years.

Published in:

Transactions of the American Fisheries Society, 2012, v. 141, n. 4, p. 1000, doi. 10.1080/00028487.2012.675893

By:

Stanley, Charles E.;
Taylor, Jason M.;
King, Ryan S.

Publication type:

Article

From Disease Association to Risk Assessment: An Optimistic View from Genome-Wide Association Studies on Type 1 Diabetes.

Published in:

PLoS Genetics, 2009, v. 5, n. 10, p. 1, doi. 10.1371/journal.pgen.1000678

By:

Zhi Wei;
Kai Wang;
Hui-Qi Qu;
Haitao Zhang;
Bradfield, Jonathan;
Kim, Cecilia;
Frackleton, Edward;
Cuiping Hou;
Glessner, Joseph T.;
Chiavacci, Rosetta;
Stanley, Charles;
Monos, Dimitri;
Grant, Struan F. A.;
Polychronakos, Constantin;
Hakonarson, Hakon

Publication type:

Article

Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations.

Published in:

2008

By:

Pinney, Sara E.;
MacMullen, Courtney;
Becker, Susan;
Yu-Wen Lin;
Hanna, Cheryl;
Thornton, Paul;
Ganguly, Arupa;
Show-Ling Shyng;
Stanley, Charles A.;
Lin, Yu-Wen;
Shyng, Show-Ling

Publication type:

journal article

Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism.

Published in:

2006

By:

Suchi, Mariko;
MacMullen, Courtney M.;
Thornton, Paul S.;
Adzick, N. Scott;
Ganguly, Arupa;
Ruchelli, Eduardo D.;
Stanley, Charles A.

Publication type:

journal article

International Guidelines for the Diagnosis and Management of Hyperinsulinism.

Published in:

Hormone Research in Paediatrics, 2024, v. 97, n. 3, p. 279, doi. 10.1159/000531766

By:

De Leon, Diva D.;
Arnoux, Jean Baptiste;
Banerjee, Indraneel;
Bergada, Ignacio;
Bhatti, Tricia;
Conwell, Louise S.;
Fu, Junfen;
Flanagan, Sarah E.;
Gillis, David;
Meissner, Thomas;
Mohnike, Klaus;
Pasquini, Tai L.S.;
Shah, Pratik;
Stanley, Charles A.;
Vella, Adrian;
Yorifuji, Tohru;
Thornton, Paul S.

Publication type:

Article

Congenital Hyperinsulinism: An Historical Perspective.

Published in:

Hormone Research in Paediatrics, 2022, v. 95, n. 6, p. 631, doi. 10.1159/000526442

By:

Thornton, Paul S.;
Stanley, Charles A.;
De Leon, Diva D.

Publication type:

Article

Mosaic GLUD1 Mutations Associated with Hyperinsulinism Hyperammonemia Syndrome.

Published in:

Hormone Research in Paediatrics, 2022, v. 95, n. 5, p. 492, doi. 10.1159/000526203

By:

Boodhansingh, Kara E.;
Rosenfeld, Elizabeth;
Lord, Katherine;
Adzick, N. Scott;
Bhatti, Tricia;
Ganguly, Arupa;
De Leon, Diva D.;
Stanley, Charles A.

Publication type:

Article

Congenital Hyperinsulinism in Infants with Turner Syndrome: Possible Association with Monosomy X and <bold>KDM6A</bold> Haploinsufficiency.

Published in:

Hormone Research in Paediatrics, 2018, v. 89, n. 6, p. 413, doi. 10.1159/000488347

By:

Gibson, Christopher E.;
Boodhansingh, Kara E.;
Li, Changhong;
Conlin, Laura;
Chen, Pan;
Becker, Susan A.;
Bhatti, Tricia;
Bamba, Vaneeta;
Adzick, N. Scott;
De Leon, Diva D.;
Ganguly, Arupa;
Stanley, Charles A.

Publication type:

Article

Dominant Form of Congenital Hyperinsulinism Maps to HK1 Region on 10q.

Published in:

Hormone Research in Paediatrics, 2013, v. 80, n. 1, p. 18, doi. 10.1159/000351943

By:

Pinney, Sara E.;
Ganapathy, Karthik;
Bradfield, Jonathan;
Stokes, David;
Sasson, ariella;
Mackiewicz, Katarzyna;
Boodhansingh, Kara;
Hughes, Nkecha;
Becker, Susan;
Givler, Stephanie;
Macmullen, Courtney;
Monos, Dimitrios;
Ganguly, arupa;
Hakonarson, Hakon;
Stanley, Charles a.

Publication type:

Article

Prenatal diagnosis and postnatal management of diffuse congenital hyperinsulinism: a case report.

Published in:

2006

By:

Peranteau, William H.;
Ganguly, Arupa;
Steinmuller, Laura;
Thornton, Paul;
Johnson, Mark P.;
Howell, Lori J.;
Stanley, Charles A.;
Adzick, N. Scott

Publication type:

journal article

Glycogen Storage Disease.

Published in:

Journal of Pediatric Gastroenterology & Nutrition, 1984, v. 3, n. 1, p. 81

By:

Yudkoff, Marc;
Nissim, Itzhak;
Stanley, Charles;
Baker, Lester;
Segal, Stanton

Publication type:

Article

The value of radiologic interventions and (18)F-DOPA PET in diagnosing and localizing focal congenital hyperinsulinism: systematic review and meta-analysis.

Published in:

2013

By:

Blomberg BA;
Moghbel MC;
Saboury B;
Stanley CA;
Alavi A;
Blomberg, Björn A;
Moghbel, Mateen C;
Saboury, Babak;
Stanley, Charles A;
Alavi, Abass

Publication type:

journal article

The Value of Radiologic Interventions and F-DOPA PET in Diagnosing and Localizing Focal Congenital Hyperinsulinism: Systematic Review and Meta-Analysis.

Published in:

Molecular Imaging & Biology, 2013, v. 15, n. 1, p. 97, doi. 10.1007/s11307-012-0572-0

By:

Blomberg, Björn;
Moghbel, Mateen;
Saboury, Babak;
Stanley, Charles;
Alavi, Abass

Publication type:

Article

CAUSES OF IN-FACEPIECE SAMPLING BIAS—I. HALF-FACEPIECE RESPIRATORS*.

Published in:

Annals of Occupational Hygiene, 1988, v. 32, n. 3, p. 345

By:

MYERS, WARREN R.;
ALLENDER, JOAN R.;
ISKANDER, WAFIK;
STANLEY, CHARLES

Publication type:

Article

The effect of postnatal depression on motherinfant interaction, infant response to the Still-face perturbation, and performance on an Instrumental Learning task.

Published in:

Development & Psychopathology, 2004, v. 16, n. 1, p. 1, doi. 10.1017/s0954579404044384

By:

CHARLES STANLEY;
LYNNE MURRAY;
ALAN STEIN

Publication type:

Article

Genetic heterogeneity in familial hyperinsulinism.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 7, p. 1119, doi. 10.1093/hmg/7.7.1119

By:

Nestorowicz, Ann;
Glaser, Benjamin;
Wilson, Beth A.;
Shyng, Show‐Ling;
Nichols, Colin G.;
Stanley, Charles A.;
Thornton, Paul S.;
Permutt, M. Alan

Publication type:

Article

Mutations in the Sulfonylurea Receptor Gene Are Associated with Familial Hyperinsulinism in Ashkenazi Jews.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 11, p. 1813, doi. 10.1093/hmg/5.11.1813

By:

Nestorowicz, Ann;
Wilson, Beth Anne;
Schoor, Kathleen P.;
Inoue, Hiroshi;
Glaser, Benjamin;
Landau, Heddy;
Stanley, Charles A.;
Thornton, Paul S.;
Clement, John P.;
Bryan, Joseph;
Aguilar-Bryan, Lydia;
Permutt, M. Alan

Publication type:

Article

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.

Published in:

Human Molecular Genetics, 1995, v. 4, n. 11, p. 2187

By:

Glaser, Benjamin;
Chiu, Ken C.;
Liu, Li;
Anker, Roberto;
Nestorowicz, Ann;
Cox, Nancy J.;
Landau, Heddy;
Kaiser, Nurit;
Thornton, Paul S.;
Stanley, Charles A.;
Cerasi, Erol;
Baker, Lester;
Donis-Keller, Helen;
Permutt, M.Alan

Publication type:

Article

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.

Published in:

Human Molecular Genetics, 1995, v. 4, n. 5, p. 879

By:

Glaser, Benjamin;
Chiu, Ken C.;
Liu, Li;
Anker, Roberto;
Nestorowicz, Ann;
Cox, Nancy J.;
Landau, Heddy;
Nurit, Kalser;
Thornton, Paul S.;
Stanley, Charles A.;
Cerasl, Erol;
Baker, Lester;
Donis-Keller, Helen;
Permutt, M.Alan

Publication type:

Article

Glutamate Dehydrogenase, a Complex Enzyme at a Crucial Metabolic Branch Point.

Published in:

Neurochemical Research, 2019, v. 44, n. 1, p. 117, doi. 10.1007/s11064-017-2428-0

By:

Smith, Hong Q.;
Li, Changhong;
Stanley, Charles A.;
Smith, Thomas James

Publication type:

Article

Glutamate Dehydrogenase: Structure, Allosteric Regulation, and Role in Insulin Homeostasis.

Published in:

Neurochemical Research, 2014, v. 39, n. 3, p. 433, doi. 10.1007/s11064-013-1173-2

By:

Li, Ming;
Li, Changhong;
Allen, Aron;
Stanley, Charles;
Smith, Thomas

Publication type:

Article

Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake.

Published in:

Annals of Neurology, 1991, v. 30, n. 5, p. 709, doi. 10.1002/ana.410300512

By:

Stanley, Charles A.;
DeLeeuw, Susan;
Coates, Paul M.;
Vianey-Liaud, Christine;
Divry, Priscille;
Bonnefont, Jean-Paul;
Saudubray, Jean-Marie;
Haymond, Morey;
Trefz, Friedrich K.;
Breningstall, Galen N.;
Wappner, Rebecca S.;
Byrd, Dennis J.;
Sansaricq, Claude;
Tein, Ingrid;
Grover, Warren;
Valle, David;
Rutledge, S. Lane;
Treem, William R.

Publication type:

Article

The Diagnosis of Ectopic Focal Hyperinsulinism of Infancy with [18F]-Dopa Positron Emission Tomography.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 8, p. 2839, doi. 10.1210/jc.2006-0455

By:

Hussain, Khalid;
Seppänen, Marko;
Näntö-Salonen, Kirsti;
Adzick, N. Scott;
Stanley, Charles A.;
Thornton, Paul;
Minn, Heikki

Publication type:

Article

Genotype-phenotype correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genes.

Published in:

2005

By:

Henwood, Maria J;
Kelly, Andrea;
Macmullen, Courtney;
Bhatia, Pooja;
Ganguly, Arupa;
Thornton, Paul S;
Stanley, Charles A

Publication type:

journal article

Familial leucine-sensitive hypoglycemia of infancy due to a dominant mutation of the beta-cell sulfonylurea receptor.

Published in:

2004

By:

Magge, Sheela N;
Shyng, Show-Ling;
MacMullen, Courtney;
Steinkrauss, Linda;
Ganguly, Arupa;
Katz, Lorraine E L;
Stanley, Charles A

Publication type:

journal article

Acute Insulin Responses to Calcium and Tolbutamide Do Not Differentiate Focal from Diffuse Congenital Hyperinsulinism.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 2, p. 925, doi. 10.1210/jc.2003-030941

By:

GIURGEA, IRINA;
LABORDE, KATHLEEN;
TOUATI, GUY;
BELLANNÉ-CHANTELOT, CHRISTINE;
NASSOGNE, MARIE-CECILE;
SEMPOUX, CHRISTINE;
JAUBERT, FRANCIS;
NGUYEN KHOA;
CHIGOT, VALERIE;
RAHIER, JACQUES;
BRUNELLE, FRANCIS;
NIHOUL-FÉKÉTÉ, CLAIRE;
DUNNE, MARK J.;
STANLEY, CHARLES;
SAUDUBRAY, JEAN-MARIE;
ROBERT, JEAN-JACQUES;
DE LONLAY, PASCALE

Publication type:

Article

Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulation.

Published in:

2004

By:

Stanley, Charles A.;
Thornton, Paul S.;
Ganguly, Arupa;
MacMullen, Courtney;
Underwood, Patricia;
Bhatia, Pooja;
Steinkrauss, Linda;
Wanner, Laura;
Kaye, Robin;
Ruchelli, Eduardo;
Suchi, Mariko;
Adzick, N Scott

Publication type:

journal article

Editorial: Advances in Diagnosis and Treatment of Hyperinsulinism in Infants and Children.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 11, p. 4857, doi. 10.1210/jc.2002-021403

By:

Stanley, Charles A.

Publication type:

Article

Hyperinsulinism/Hyperammonemia Syndrome in Children with Regulatory Mutations in the Inhibitory Guanosine Triphosphate-Binding Domain of Glutamate Dehydrogenase.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 4, p. 1782, doi. 10.1210/jcem.86.4.7414

By:

MACMULLEN, COURTNEY;
FANG, JIE;
HSU, BETTY Y. L.;
KELLY, ANDREA;
DE LONLAY-DEBENEY, PASCALE;
SAUDUBRAY, JEAN-MARIE;
GANGULY, ARUPA;
SMITH, THOMAS J.;
STANLEY, CHARLES A.

Publication type:

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.

Published in:

1999

By:

LEVITT KATZ, LORRAINE E.;
FERRY JR., ROBERT J.;
STANLEY, CHARLES A.;
COLLETT-SOLBERG, PAULO F.;
BAKER, LESTER;
COHEN, PINCHAS

Publication type:

journal article

Dual Regulation of Insulin-Like Growth Factor Binding Protein-1 Levels by Insulin and Cortisol during Fasting.

Published in:

Journal of Clinical Endocrinology & Metabolism, 1998, v. 83, n. 12, p. 4426, doi. 10.1210/jcem.83.12.5347

By:

LEVITT KATZ, LORRAINE E.;
SATIN-SMITH, MARTA S.;
COLLETT-SOLBERG, PAULO;
BAKER, LESTER;
STANLEY, CHARLES A.;
COHEN, PINCHAS

Publication type:

Article

Hyperinsulinismus bei Säuglingen und Kindern: wenn ein Insulinspiegel nicht immer ausreicht / Hyperinsulinism in infancy and childhood: when an insulin level is not always enough1).

Published in:

Journal of Laboratory Medicine / Laboratoriums Medizin, 2009, v. 33, n. 3, p. 166, doi. 10.1515/JLM.2009.020

By:

Palladino, Andrew A.;
Bennett, Michael J.;
Stanley, Charles A.

Publication type:

Article

Clinical heterogeneity of hyperinsulinism due to HNF1A and HNF4A mutations.

Published in:

Pediatric Diabetes, 2018, v. 19, n. 5, p. 910, doi. 10.1111/pedi.12655

By:

Tung, Joanna Yuet‐ling;
Boodhansingh, Kara;
Stanley, Charles A.;
De León, Diva D.

Publication type:

Article

A severe case of hyperinsulinism due to hemizygous activating mutation of glutamate dehydrogenase.

Published in:

Pediatric Diabetes, 2017, v. 18, n. 8, p. 911, doi. 10.1111/pedi.12507

By:

Barrosse‐Antle, Mary;
Su, Chang;
Chen, Pan;
Boodhansingh, Kara E;
Smith, Thomas J;
Stanley, Charles A;
De León, Diva D;
Li, Changhong

Publication type:

Article

Congenital Hypoglycemia Disorders: New Aspects of Etiology, Diagnosis, Treatment and Outcomes.

Published in:

Pediatric Diabetes, 2017, v. 18, n. 1, p. 3, doi. 10.1111/pedi.12453

By:

De Leon, Diva D.;
Stanley, Charles A.

Publication type:

Article

Necrotizing enterocolitis in neonates receiving octreotide for the management of congenital hyperinsulinism.

Published in:

Pediatric Diabetes, 2010, v. 11, n. 2, p. 142, doi. 10.1111/j.1399-5448.2009.00547.x

By:

Laje, Pablo;
Halaby, Lori;
Adzick, N. Scott;
Stanley, Charles A.

Publication type:

Article

Glutamate dehydrogenase: Structure of a hyperinsulinism mutant, corrections to the atomic model, and insights into a regulatory site.

Published in:

Proteins, 2019, v. 87, n. 1, p. 41, doi. 10.1002/prot.25620

By:

Nassar, Omneya M.;
Li, Changhong;
Stanley, Charles A.;
Pettitt, B. Montgomery;
Smith, Thomas J.

Publication type:

Article

Late effects after treatment of twenty children with soft tissue sarcomas of the head and neck. Experience at a single institution with a review of the literature.

Published in:

1986

By:

Fromm, Mitchel;
Littman, Philip;
Raney, R. Beverly;
Nelson, Linda;
Handler, Steven;
Diamond, Gary;
Stanley, Charles;
Fromm, M;
Littman, P;
Raney, R B;
Nelson, L;
Handler, S;
Diamond, G;
Stanley, C

Publication type:

journal article

Novel Hypoglycemia Phenotype in Congenital Hyperinsulinism Due to Dominant Mutations of Uncoupling Protein 2.

Published in:

2016

By:

Ferrara, Christine T;
Boodhansingh, Kara E;
Paradies, Elenora;
Giuseppe, Fiermonte;
Steinkrauss, Linda J;
Topor, Lisa Swartz;
Quintos, Jose Bernardo;
Ganguly, Arupa;
De Leon, Diva D;
Palmieri, Ferdinando;
Stanley, Charles A;
Paradies, Eleonora;
Fiermonte, Giuseppe

Publication type:

journal article

Perspective on the Genetics and Diagnosis of Congenital Hyperinsulinism Disorders.

Published in:

2016

By:

Stanley, Charles A

Publication type:

journal article