Works matching AU White, Perrin C

Results: 87

Two steroid 21-hydroxylase genes are located in the murine S region.

Published in:

Nature, 1984, v. 312, n. 5993, p. 465, doi. 10.1038/312465a0

By:

White, Perrin C.;
Chaplin, David D.;
Weis, John H.;
Dupont, Bo;
New, Maria I.;
Seidman, J. G.

Publication type:

Article

Type 2 Diabetes in a Patient With IMAGe Syndrome Secondary to Polymerase Epsilon Pathogenic Variants Open Access.

Published in:

2025

By:

Horvit, Andrew;
Mulpuri, Neha;
Mirfakhraee, Sasan;
White, Perrin C;
Abramowitz, Jessica

Publication type:

Case Study

Diabetic Ketoacidosis in a Pediatric Patient with Cystic Fibrosis–related Diabetes Open Access.

Published in:

2025

By:

Harinarayanan, Shyam;
Merritt, Taylor;
White, Perrin C

Publication type:

Case Study

In Memoriam: Maria Iandolo New, 1928-2024.

Published in:

JCEM Case Reports, 2024, v. 2, n. 12, p. 1, doi. 10.1210/jcemcr/luae186

By:

Speiser, Phyllis W;
Auchus, Richard J;
White, Perrin C

Publication type:

Article

Genetic interaction among three genomic regions creates distinct contributions to early- and late-onset type 1 diabetes mellitus.

Published in:

Pediatric Diabetes, 2005, v. 6, n. 4, p. 213, doi. 10.1111/j.1399-543X.2005.00132.x

By:

Felner, Eric I.;
Klitz, William;
Ham, Melissa;
Lazaro, Ana M.;
Stastny, Peter;
Dupont, Bo;
White, Perrin C.

Publication type:

Article

Bedside ketone determination in diabetic children with hyperglycemia and ketosis in the acute care setting.

Published in:

Pediatric Diabetes, 2004, v. 5, n. 1, p. 39, doi. 10.1111/j.1399-543X.2004.00032.x

By:

Ham, Melissa R.;
Okada, Pamela;
White, Perrin C.

Publication type:

Article

Parental Involvement and Executive Function in Emerging Adults with Type 1 Diabetes.

Published in:

2019

By:

Berg, Cynthia A;
Wiebe, Deborah J;
Tracy, Eunjin Lee;
Kelly, Caitlin S;
Mello, Daniel;
Turner, Sara L;
Butner, Jonathan E;
Munion, Ascher K;
Mansfield, Jessica H;
White, Perrin C;
Murray, Mary;
Suchy, Yana;
Lee Tracy, Eunjin

Publication type:

journal article

Adolescent Information Management and Parental Knowledge in Non-Latino White and Latino Youth Managing Type 1 Diabetes.

Published in:

2018

By:

Tucker, Christy;
Wiebe, Deborah J.;
Main, Alexandra;
Lee, Alyssa G.;
White, Perrin C.

Publication type:

journal article

Associations of Parent–Adolescent Relationship Quality With Type 1 Diabetes Management and Depressive Symptoms in Latino and Caucasian Youth.

Published in:

Journal of Pediatric Psychology, 2014, v. 39, n. 10, p. 1104, doi. 10.1093/jpepsy/jsu062

By:

Main, Alexandra;
Wiebe, Deborah J.;
Croom, Andrea R.;
Sardone, Katie;
Godbey, Elida;
Tucker, Christy;
White, Perrin C.

Publication type:

Article

Individual Differences and Day-to-Day Fluctuations in Perceived Self-Regulation Associated With Daily Adherence in Late Adolescents With Type 1 Diabetes.

Published in:

Journal of Pediatric Psychology, 2014, v. 39, n. 9, p. 1038, doi. 10.1093/jpepsy/jsu051

By:

Berg, Cynthia A.;
Wiebe, Deborah J.;
Suchy, Yana;
Hughes, Amy E.;
Anderson, Jessica H.;
Godbey, Elida I.;
Butner, Jonathan;
Tucker, Christy;
Franchow, Emilie I.;
Pihlaskari, Andrea K.;
King, Pamela S.;
Murray, Mary A.;
White, Perrin C.

Publication type:

Article

In Memoriam: Maria Iandolo New, 1928-2024.

Published in:

Endocrinology, 2024, v. 165, n. 12, p. 1, doi. 10.1210/endocr/bqae130

By:

Speiser, Phyllis W;
Auchus, Richard J;
White, Perrin C

Publication type:

Article

HSD11B2 CA-repeat and sodium balance.

Published in:

Hypertension Research, 2013, v. 36, n. 7, p. 614, doi. 10.1038/hr.2013.13

By:

Mune, Tomoatsu;
Morita, Hiroyuki;
Takada, Nobuki;
Yamamoto, Yoritsuna;
Isomura, Yukinori;
Suwa, Tetsuya;
Takeda, Jun;
White, Perrin C;
Kaku, Kohei

Publication type:

Article

The Very Large G-Protein-Coupled Receptor VLGR1: A Component of the Ankle Link Complex Required for the Normal Development of Auditory Hair Bundles.

Published in:

2006

By:

McGee, JoAnn;
Goodyear, Richard J.;
McMillan, D. Randy;
Stauffer, Eric A.;
Holt, Jeffrey R.;
Locke, Kirsten G.;
Birch, David G.;
Legan, P. Kevin;
White, Perrin C.;
Walsh, Edward J.;
Richardson, Guy P.

Publication type:

Abstract

Mutations in the genes encoding 11ß-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency.

Published in:

Nature Genetics, 2003, v. 34, n. 4, p. 434, doi. 10.1038/ng1214

By:

Draper, Nicole;
Walker, Elizabeth A.;
Bujalska, Iwona J.;
Tomlinson, Jeremy W.;
Chalder, Susan M.;
Arlt, Wiebke;
Lavery, Gareth G.;
Bedendo, Oliver;
Ray, David W.;
Laing, Ian;
Malunowicz, Ewa;
White, Perrin C.;
Hewison, Martin;
Mason, Philip J.;
Connell, John M.;
Shackleton, Cedric H.L.;
Stewart, Paul M.

Publication type:

Article

Continuous Glucose Monitor Accuracy for Diabetes Management in Hospitalized Children.

Published in:

Diabetes Care, 2025, v. 48, n. 2, p. 259, doi. 10.2337/dc24-1562

By:

Garg, Neha;
Lewis, Kamryn;
White, Perrin C.;
Adhikari, Soumya

Publication type:

Article

Executive Function Predicting Longitudinal Change in Type 1 Diabetes Management During the Transition to Emerging Adulthood.

Published in:

2018

By:

Berg, Cynthia A.;
Wiebe, Deborah J.;
Suchy, Yana;
Turner, Sara L.;
Butner, Jonathan;
Munion, Ascher;
Lansing, Amy Hughes;
White, Perrin C.;
Murray, Mary

Publication type:

journal article

Ontogeny of adrenal steroid biosynthesis: why girls will be girls.

Published in:

Journal of Clinical Investigation, 2006, v. 116, n. 4, p. 872, doi. 10.1172/JCI28296

By:

White, Perrin C.

Publication type:

Article

In Memoriam: Maria Iandolo New, 1928-2024.

Published in:

Journal of the Endocrine Society, 2024, v. 8, n. 12, p. 1, doi. 10.1210/jendso/bvae167

By:

Speiser, Phyllis W;
Auchus, Richard J;
White, Perrin C

Publication type:

Article

Precocious Puberty in a Boy With Bilateral Leydig Cell Tumors due to a Somatic Gain-of-Function LHCGR Variant.

Published in:

Journal of the Endocrine Society, 2022, v. 6, n. 10, p. 1, doi. 10.1210/jendso/bvac127

By:

Flippo, Chelsi;
Kolli, Vipula;
Andrew, Melissa;
Berger, Seth;
Bhatti, Tricia;
Boyce, Alison M;
Casella, Daniel;
Collins, Michael T;
Délot, Emmanuèle;
Devaney, Joseph;
Hewitt, Stephen M;
Kolon, Thomas;
Mallappa, Ashwini;
White, Perrin C;
Merke, Deborah P;
Dauber, Andrew

Publication type:

Article

Referrals for Elevated Thyroid Stimulating Hormone to Pediatric Endocrinologists.

Published in:

Journal of the Endocrine Society, 2019, v. 3, n. 11, p. 2032, doi. 10.1210/js.2019-00244

By:

Gammons, Sarah;
Presley, Brent K;
White, Perrin C

Publication type:

Article

Weight gain after treatment of Graves' disease in children.

Published in:

Clinical Endocrinology, 2018, v. 88, n. 1, p. 66, doi. 10.1111/cen.13493

By:

Alonso, Guy Todd;
Rabon, Shona;
White, Perrin C.

Publication type:

Article

Risk factors for hospitalization of children with congenital adrenal hyperplasia.

Published in:

Clinical Endocrinology, 2017, v. 86, n. 5, p. 669, doi. 10.1111/cen.13309

By:

Yang, Ming;
White, Perrin C.

Publication type:

Article

Graves' disease in children: long-term outcomes of medical therapy.

Published in:

Clinical Endocrinology, 2016, v. 85, n. 4, p. 632, doi. 10.1111/cen.13099

By:

Rabon, Shona;
Burton, Amy M.;
White, Perrin C.

Publication type:

Article

Possible association but no linkage of the HSD11B2 gene encoding the kidney isozyme of 11β-hydroxysteroid dehydrogenase to hypertension in Black people.

Published in:

Clinical Endocrinology, 2001, v. 55, n. 2, p. 249, doi. 10.1046/j.1365-2265.2001.01314.x

By:

White, Perrin C.;
Agarwal, Anil K.;
Li, Airong;
Nikkila, Heli;
Pratt, J. Howard;
Caulfield, Mark;
Clark, Adrian;
McTernan, Claire;
Stewart, Paul M.

Publication type:

Article

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.

Published in:

Clinical Endocrinology, 1998, v. 49, n. 4, doi. 10.1046/j.1365-2265.1998.00559.x

By:

Speiser, Phyllis W.;
White, Perrin C.

Publication type:

Article

A Brief History of Congenital Adrenal Hyperplasia.

Published in:

Hormone Research in Paediatrics, 2022, v. 95, n. 6, p. 529, doi. 10.1159/000526468

By:

Miller, Walter L.;
White, Perrin C.

Publication type:

Article

Alterations of Cortisol Metabolism in Human Disorders.

Published in:

Hormone Research in Paediatrics, 2018, v. 89, n. 5, p. 320, doi. 10.1159/000485508

By:

White, Perrin C.

Publication type:

Article

A Randomized Controlled Trial Comparing Motivational Interviewing in Education to Structured Diabetes Education in Teens With Type 1 Diabetes.

Published in:

Diabetes Care, 2010, v. 33, n. 8, p. 1741, doi. 10.2337/dc10-0019

By:

Wang, Yu-Chi;
Stewart, Sunita M.;
MacKenzie, Marsha;
Nakonezny, Paul A.;
Edwards, Deidre;
White, Perrin C.

Publication type:

Article

Molecular Cloning of Steroid 21-Hydroxylasea.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 277, doi. 10.1111/j.1749-6632.1985.tb14613.x

By:

WHITE, PERRIN C.;
NEW, MARIA I.;
DUPONT, BO

Publication type:

Article

Cloning and Expression of cDNA Encoding a Bovine Adrenal Cytochrome P-450 Specific for Steroid 21-Hydroxylation (P-450C21)a.

Published in:

Annals of the New York Academy of Sciences, 1984, v. 435, n. 1, p. 229, doi. 10.1111/j.1749-6632.1984.tb13778.x

By:

WHITE, PERRIN C.;
NEW, MARIA I.;
DUPONT, BO

Publication type:

Article

Autosomal recessive familial neurohypophyseal diabetes insipidus with continued secretion of mutant weakly active vasopressin.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 7, p. 1303, doi. 10.1093/hmg/8.7.1303

By:

Willcutts, Michael D.;
Felner, Eric;
White, Perrin C.

Publication type:

Article

CYP11B1 Mutations Causing Non-Classic Adrenal Hyperplasia due to 11β-Hydroxylase Deficiency.

Published in:

Human Molecular Genetics, 1997, v. 6, n. 11, p. 1829, doi. 10.1093/hmg/6.11.1829

By:

Joehrer, Karin;
Geley, Stephan;
Strasser-Wozak, Elisabeth M.C.;
Azziz, Ricardo;
Wollmann, Hartmut A.;
Schmitt, Klaus;
Kofler, Reinhard;
White, Perrin C.

Publication type:

Article

Identification of Non-Amplifying CYP21 Genes When Using PCR-Based Diagnosis of 21-Hydroxylase Deficiency in Congenital Adrenal Hyperplasia (CAH) Affected Pedigrees.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 12, p. 2039, doi. 10.1093/hmg/5.12.2039

By:

Day, Darren J.;
Speiser, Phyllis W.;
Schulze, Egbert;
Bettendorf, M.;
Fitness, Jodene;
Barany, Francis;
White, Perrin C.

Publication type:

Article

A Summary of the Endocrine Society Clinical Practice Guidelines on Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency.

Published in:

International Journal of Pediatric Endocrinology, 2010, p. 1, doi. 10.1155/2010/494173

By:

Speiser, Phyllis W.;
Azziz, Ricardo;
Baskin, Laurence S.;
Ghizzoni, Lucia;
Hensle, Terry W.;
Merke, Deborah P.;
Meyer-Bahlburg, Heino F. L.;
Miller, Walter L.;
Montori, Victor M.;
Oberfield, Sharon E.;
Ritzen, Martin;
White, Perrin C.

Publication type:

Article

Gene Expression in Peripheral Blood Mononuclear Cells from Children with Diabetes.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 9, p. 3705, doi. 10.1210/jc.2007-0979

By:

Kaizer, Ellen C.;
Glaser, Casey L.;
Chaussabel, Damien;
Banchereau, Jacques;
Pascual, Virginia;
White, Perrin C.

Publication type:

Article

Elevated Expression of Luteinizing Hormone Receptor in Aldosterone-Producing Adenomas.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 3, p. 1136, doi. 10.1210/jc.2005-1298

By:

Saner-Amigh, Karla;
Mayhew, Bobbie A.;
Mantero, Franco;
Schiavi, Francesca;
White, Perrin C.;
Rao, Chalama V.;
Rainey, William E.

Publication type:

Article

Association of Lys173Arg Polymorphism with CYP11B2 Expression in Normal Adrenal Glands and AldosteroneProducing Adenomas.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 11, p. 6226, doi. 10.1210/jc.2005-0299

By:

Hiromichi Tanahashi;
Tomoatsu Mune;
Yoshito Takahashi;
Mako Isaji;
Tetsuya Suwa;
Hiroyuki Morita;
Noriyoshi Yamakita;
Keigo Yasuda;
Takashi Deguchi;
White, Perrin C.;
Jun Takeda

Publication type:

Article

Genotypes at 11β-Hydroxysteroid Dehydrogenase Type 11B1 and Hexose-6-Phosphate Dehydrogenase Loci Are Not Risk Factors for Apparent Cortisone Reductase Deficiency in a Large Population-Based Sample.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 10, p. 5880, doi. 10.1210/jc.2005-0942

By:

White, Perrin C.

Publication type:

Article

Expression Profiles for Steroidogenic Enzymes in Adrenocortical Disease.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 9, p. 5446, doi. 10.1210/jc.2005-0836

By:

Bassett, Mary H.;
Mayhew, Bobbie;
Rehman, Khurram;
White, Perrin C.;
Mantero, Franco;
Arnaldi, Giorgio;
Stewart, Paul M.;
Bujalska, Iwona;
Rainey, William E.

Publication type:

Article

Editorial: Polymorphisms in CYP11B Genes and 11-Hydroxylase Activity.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 2, p. 1252, doi. 10.1210/jc.2004-2452

By:

White, Perrin C.;
Rainey, William E.

Publication type:

Article

Aldosterone: Direct Effects on and Production by the Heart.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 6, p. 2376, doi. 10.1210/jc.2003-030373

By:

WHITE, PERRIN C.

Publication type:

Article

Role of Local 11β-Hydroxysteroid Dehydrogenase Type 2 Expression in Determining the Phenotype of Adrenal Adenomas.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 2, p. 864, doi. 10.1210/jc.2001-011335

By:

TOMOATSU MUNE;
HIROYUKI MORITA;
TAKASHI SUZUKI;
YOSHIHITO TAKAHASHI;
YUKINORI ISOMURA;
TETSUYA TANAHASHI;
HISASHI DAIDO;
NORIYOSHI YAMAKITA;
TAKASHI DEGUCHI;
HIRONOBU SASANO;
WHITE, PERRIN C.;
KEIGO YASUDA

Publication type:

Article

Congenital Hyperreninemic Hypoaldosteronism Unlinked to the Aldosterone Synthase (CYP11B2) Gene.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 11, p. 5379, doi. 10.1210/jcem.86.11.8005

By:

KAYES-WANDOVER, KATHLEEN M.;
TANNIN, GRACE M.;
SHULMAN, DOROTHY;
PELED, DROR;
JONES, KENNETH L.;
KARAVITI, LEFKOTHEA;
WHITE, PERRIN C.

Publication type:

Article

Type 1 Aldosterone Synthase Deficiency Presenting in a Middle-Aged Man*.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 3, p. 1008, doi. 10.1210/jcem.86.3.7326

By:

KAYES-WANDOVER, KATHLEEN M.;
LEE SCHINDLER, R. E.;
TAYLOR, HARRIS C.;
WHITE, PERRIN C.

Publication type:

Article

Steroidogenic Enzyme Gene Expression in the Human Heart.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 7, p. 2519, doi. 10.1210/jcem.85.7.6663

By:

KAYES-WANDOVER, KATHLEEN M.;
WHITE, PERRIN C.

Publication type:

Article

Comment on congenital adrenal hyperplasia without demonstrable genetic mutations.

Published in:

1999

By:

White, Perrin C.

Publication type:

Letter

CYP11B1 Mutations Causing Congenital Adrenal Hyperplasia due to 11β-Hydroxylase Deficiency.

Published in:

Journal of Clinical Endocrinology & Metabolism, 1996, v. 81, n. 8, p. 2896, doi. 10.1210/jc.81.8.2896

By:

GELEY, STEPHAN;
KAPELARI, KLAUS;
JOHRER, KARIN;
PETER, MICHAEL;
GLATZL, JOSEF;
VIERHAPPER, HEINRICH;
SCHWARZ, SIEGFRIED;
HELMBERG, ARNO;
SIPPELL, WOLFGANG G.;
WHITE, PERRIN C.;
KOFLER, REINHARD

Publication type:

Article

P53 and Cellular Glucose Uptake.

Published in:

Endocrine Research, 2013, v. 38, n. 1, p. 32, doi. 10.3109/07435800.2012.710883

By:

de la Torre, Alejandro J.;
Rogoff, Daniela;
White, Perrin C.

Publication type:

Article

A Role for the NGFI-B Family in Adrenal Zonation and Adrenocortical Disease.

Published in:

Endocrine Research, 2004, v. 30, n. 4, p. 567, doi. 10.1081/ERC-200043715

By:

Bassett, Mary H.;
White, Perrin C.;
Rainey, William E.

Publication type:

Article

ROLE OF LOCAL 11β-HYDROXYSTEROID DEHYDROGENASE TYPE 2 (HSD11B2) EXPRESSION IN DETERMINING THE PHENOTYPE OF ADRENAL ADENOMAS.

Published in:

Endocrine Research, 2002, v. 28, n. 4, p. 751, doi. 10.1081/ERC-120017001

By:

Mune, Tomoatsu;
Morita, Hiroyuki;
Suzuki, Takashi;
Takahashi, Yoshihito;
Isomura, Yukinori;
Tanahashi, Tetsuya;
Daido, Hisashi;
Yamakita, Noriyoshi;
Deguchi, Takashi;
Sasano, Hironobu;
Yasuda, Keigo;
White, Perrin C.

Publication type:

Article