Phyllis Speiser

Biosketch / Results /

Phyllis Speiser, M.D.

Adjunct Professor;
Department of Pediatrics (Pediatrics)

Contact Info

Address
269-01 76th Ave.
Schneider Children's Hospital
New Hyde Park, NY 11040

718-470-3290
718-470-4565
Phyllis.Speiser@nyumc.org

« Back to Results

Education

1979-1982 — Internship and Residency Bronx Municipal Hospital Center-Albert Einstein College of Medicine, Residency

« Back to Results

Research Interests

Molecular genetic and clinical aspects of adrenal disease and steroid hormone biosynthesis.

« Back to Results

All data from NYU Health Sciences Library Faculty Bibliography — -

Contact:
http://hsl.med.nyu.edu/faculty-bibliography-search

Plasma advanced glycation end products (AGEs), receptors for AGEs and their correlation with inflammatory markers in middle school-age children
Accacha, S; Rosenfeld, W; Jacobson, A; Michel, L; Schnurr, F J; Shelov, S; Ten, S; Boucher-Berry, C; Carey, D E; Speiser, P W; Lowell, B; Conroy, R; Klein, M; Fennoy, I; Rapaport, R; Rosenbaum, M
2013 ;80(5):318-327, Hormone research in paediatrics
— id: 845162, year: 2013, vol: 80, page: 318, stat: Journal Article,

Effects of parental origins and length of residency on adiposity measures and nutrition in urban middle school students: a cross-sectional study
Kuryan, Ranita; Frankel, David; Cervoni, Barbie; Koltun, Audrey; Lowell, Barbara; Altshuler, Lisa; Rosenbaum, Michael; Shelov, Steven P; Carey, Dennis E; Accacha, Siham; Fennoy, Ilene; Rapaport, Robert; Rosenfeld, Warren; Ten, Svetlana; Speiser, Phyllis W
2013 Oct;2013(1):16-16, International journal of pediatric endocrinology
— id: 845002, year: 2013, vol: 2013, page: 16, stat: Journal Article,

Racial/ethnic Differences in Clinical and Biochemical Type 2 Diabetes Mellitus Risk Factors in Children
Rosenbaum, Michael; Fennoy, Ilene; Accacha, Siham; Altshuler, Lisa; Carey, Dennis E; Holleran, Steven; Rapaport, Robert; Shelov, Steven P; Speiser, Phyllis W; Ten, S; Bhangoo, Amrit; Boucher-Berry, Claudia; Espinal, Yomery; Gupta, Rishi; Hassoun, Abeer A; Iazetti, Loretta; Jacques, Fabien J; Jean, Amy M; Klein, Michelle L; Levine, Robert; Lowell, Barbara; Michel, Lesley; Rosenfeld, Warren
2013 Apr;:2081-2090, Obesity (Silver Spring)
— id: 306552, year: 2013, vol: , page: 2081, stat: Journal Article,

Vitamin D, osteocalcin and risk for adiposity as co-morbidities in middle school children
Boucher-Berry C; Speiser PW; Carey DE; Shelov SP; Accacha S; Fennoy I; Rapaport R; Espinal Y; Rosenbaum M
2012 Nov 8;:283-293, Journal of bone & mineral research
— id: 143667, year: 2012, vol: , page: 283, stat: Journal Article,

Treatment outcomes in congenital adrenal hyperplasia
Cheng, Tina Q; Speiser, Phyllis W
2012 ;59(1):269-281, Advances in pediatrics
— id: 845072, year: 2012, vol: 59, page: 269, stat: Journal Article,

Retinol binding protein 4 is associated with adiposity-related co-morbidity risk factors in children
Conroy, Rushika; Espinal, Yomery; Fennoy, Ilene; Accacha, Siham; Boucher-Berry, Claudia; Carey, Dennis E; Close, Sharron; DeSantis, Deborah; Gupta, Rishi; Hassoun, Abeer A; Iazzetti, Loretta; Jacques, Fabean J; Jean, Amy M; Michel, Lesly; Pavlovich, Katherine; Rapaports, Robert; Rosenfeld, Warren; Shamoon, Elisabeth; Shelov, Steven; Speiser, Phyllis W; Ten, Svetlana; Rosenbaum, Michael
2011 ;24(11-12):913-919, Journal of pediatric endocrinology & metabolism
— id: 845062, year: 2011, vol: 24, page: 913, stat: Journal Article,

Medical treatment of classic and nonclassic congenital adrenal hyperplasia
Speiser, Phyllis W
2011 ;707:41-45, Advances in experimental medicine & biology
— id: 845022, year: 2011, vol: 707, page: 41, stat: Journal Article,

Congenital adrenal hyperplasia: an update in children
Trapp, Christine M; Speiser, Phyllis W; Oberfield, Sharon E
2011 Jun;18(3):166-170, Current opinion in endocrinology, diabetes, & obesity
— id: 145509, year: 2011, vol: 18, page: 166, stat: Journal Article,

Guidelines for the Development of Comprehensive Care Centers for Congenital Adrenal Hyperplasia: Guidance from the CARES Foundation Initiative
Auchus, Richard J; Witchel, Selma Feldman; Leight, Kelly R; Aisenberg, Javier; Azziz, Ricardo; Bachega, Tania A; Baker, Linda A; Baratz, Arlene B; Baskin, Laurence S; Berenbaum, Sheri A; Breault, David T; Cerame, Barbara I; Conway, Gerard S; Eugster, Erica A; Fracassa, Stephanie; Gearhart, John P; Geffner, Mitchell E; Harris, Katharine B; Hurwitz, Richard S; Katz, Aviva L; Kalro, Brinda N; Lee, Peter A; Alger Lin, Gretchen; Loechner, Karen J; Marshall, Ian; Merke, Deborah P; Migeon, Claude J; Miller, Walter L; Nenadovich, Tamara L; Oberfield, Sharon E; Pass, Kenneth A; Poppas, Dix P; Lloyd-Puryear, Michele A; Quigley, Charmian A; Riepe, Felix G; Rink, Richard C; Rivkees, Scott A; Sandberg, David E; Schaeffer, Traci L; Schlussel, Richard N; Schneck, Francis X; Seely, Ellen W; Snyder, Diane; Speiser, Phyllis W; Therrell, Bradford L; Vanryzin, Carol; Vogiatzi, Maria G; Wajnrajch, Michael P; White, Perrin C; Zuckerman, Alan E
2010 ;2010:275213-275213, International journal of pediatric endocrinology
— id: 145520, year: 2010, vol: 2010, page: 275213, stat: Journal Article,

Growth and development: congenital adrenal hyperplasia-glucocorticoids and height
Speiser, Phyllis W
2010 Jan;6(1):14-15, Nature reviews. Endocrinology
— id: 845012, year: 2010, vol: 6, page: 14, stat: Journal Article,

A Summary of the Endocrine Society Clinical Practice Guidelines on Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency
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
2010 ;2010:494173-494173, International journal of pediatric endocrinology
— id: 145521, year: 2010, vol: 2010, page: 494173, stat: Journal Article,

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline
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
2010 Sep;95(9):4133-4160, Journal of clinical endocrinology & metabolism
— id: 145516, year: 2010, vol: 95, page: 4133, stat: Journal Article,

Poor glycemic control is associated with abnormal changes in 24-hour ambulatory blood pressure in children and adolescents with type 1 diabetes mellitus
Chatterjee, Manjula; Speiser, Phyllis W; Pellizzarri, Margaret; Carey, Dennis E; Fort, Pavel; Kreitzer, Paula M; Frank, Graeme R
2009 Nov;22(11):1061-1067, Journal of pediatric endocrinology & metabolism
— id: 845052, year: 2009, vol: 22, page: 1061, stat: Journal Article,

Pitfalls in the measurement of the nocturnal blood pressure dip in adolescents with type 1 diabetes
Delaney, Angela; Pellizzari, Margaret; Speiser, Phyllis W; Frank, Graeme R
2009 Jan;32(1):165-168, Diabetes care
— id: 94834, year: 2009, vol: 32, page: 165, stat: Journal Article,

Managing childhood overweight: behavior, family, pharmacology, and bariatric surgery interventions
Latzer, Yael; Edmunds, Laurel; Fenig, Silvana; Golan, Moria; Gur, Eitan; Hochberg, Ze'ev; Levin-Zamir, Diane; Zubery, Eynat; Speiser, Phyllis W; Stein, Daniel
2009 Mar;17(3):411-423, Obesity (Silver Spring)
— id: 94833, year: 2009, vol: 17, page: 411, stat: Journal Article,

Novel P450c17 Mutation H373D Causing Combined 17 alpha-Hydroxylase/17,20-Lyase Deficiency
Sahakitrungruang, T; Tee, MK; Speiser, PW; Miller, WL
2009 AUG ;94(8):3089-3092, Journal of clinical endocrinology & metabolism
— id: 101610, year: 2009, vol: 94, page: 3089, stat: Journal Article,

Novel P450c17 mutation H373D causing combined 17 alpha-hydroxylase/17,20-lyase deficiency
Sahakitrungruang, T; Tee, MK; Speiser, PW; Miller, WL
2009 NOV ;72(3):40-40, Hormone research
— id: 106179, year: 2009, vol: 72, page: 40, stat: Journal Article,

Novel P450c17 mutation H373D causing combined 17alpha-hydroxylase/17,20-lyase deficiency
Sahakitrungruang, Taninee; Tee, Meng Kian; Speiser, Phyllis W; Miller, Walter L
2009 Aug;94(8):3089-3092, Journal of clinical endocrinology & metabolism
— id: 845042, year: 2009, vol: 94, page: 3089, stat: Journal Article,

Nonclassic adrenal hyperplasia
Speiser, Phyllis W
2009 Mar;10(1):77-82, Reviews in endocrine & metabolic disorders
— id: 94836, year: 2009, vol: 10, page: 77, stat: Journal Article,

Prenatal diagnosis and treatment of congenital adrenal hyperplasia
Speiser, Phyllis W
Genetic disorders and the fetus Oxford : Wiley-Blackwell, 2009,
— id: 845192, year: 2009, vol: , page: 600, stat: Chapter,

Prevention and treatment of pediatric obesity: an endocrine society clinical practice guideline based on expert opinion
August, Gilbert P; Caprio, Sonia; Fennoy, Ilene; Freemark, Michael; Kaufman, Francine R; Lustig, Robert H; Silverstein, Janet H; Speiser, Phyllis W; Styne, Dennis M; Montori, Victor M
2008 Dec;93(12):4576-4599, Journal of clinical endocrinology & metabolism
— id: 94835, year: 2008, vol: 93, page: 4576, stat: Journal Article,

Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum
Cole, Lindsay W; Sidis, Yisrael; Zhang, ChengKang; Quinton, Richard; Plummer, Lacey; Pignatelli, Duarte; Hughes, Virginia A; Dwyer, Andrew A; Raivio, Taneli; Hayes, Frances J; Seminara, Stephanie B; Huot, Celine; Alos, Nathalie; Speiser, Phyllis; Takeshita, Akira; Van Vliet, Guy; Pearce, Simon; Crowley, William F Jr; Zhou, Qun-Yong; Pitteloud, Nelly
2008 Sep;93(9):3551-3559, Journal of clinical endocrinology & metabolism
— id: 845032, year: 2008, vol: 93, page: 3551, stat: Journal Article,

Twenty-four hour ambulatory blood pressure monitoring in adolescents with type 1 diabetes: getting started
Pellizzari, Margaret; Speiser, Phyllis W; Carey, Dennis E; Fort, Pavel; Kreitzer, Paula M; Frank, Graeme R
2008 Nov;2(6):1087-1093, Journal of diabetes science & technology
— id: 845082, year: 2008, vol: 2, page: 1087, stat: Journal Article,

Growth hormone improves growth rate and preserves renal function in Dent disease
Sheffer-Babila, Sharone; Chandra, Manju; Speiser, Phyllis W
2008 Mar;21(3):279-286, Journal of pediatric endocrinology & metabolism
— id: 94837, year: 2008, vol: 21, page: 279, stat: Journal Article,

Pamidronate treatment of hypercalcemia caused by vitamin D toxicity
Chatterjee, Manjula; Speiser, Phyllis W
2007 Nov;20(11):1241-1248, Journal of pediatric endocrinology & metabolism
— id: 94839, year: 2007, vol: 20, page: 1241, stat: Journal Article,

Interpretation of pediatric endocrine laboratory tests: pitfalls in steroid hormone measurements and genotyping
Speiser, Phyllis W
2007 Oct;5 Suppl 1:578-583, Pediatric endocrinology reviews : PER
— id: 76114, year: 2007, vol: 5 Suppl 1, page: 578, stat: Journal Article,

Prenatal and neonatal diagnosis and treatment of congenital adrenal hyperplasia
Speiser, Phyllis W
2007 ;68 Suppl 5:90-92, Hormone research
— id: 94838, year: 2007, vol: 68 Suppl 5, page: 90, stat: Journal Article,

Reproductive outcome of women with 21-hydroxylase-deficient nonclassic adrenal hyperplasia
Moran, C; Azziz, R; Weintrob, N; Witchel, S F; Rohmer, V; Dewailly, D; Marcondes, J A M; Pugeat, M; Speiser, P W; Pignatelli, D; Mendonca, B B; Bachega, T A S; Escobar-Morreale, H F; Carmina, E; Fruzzetti, F; Kelestimur, F
2006 Sep;91(9):3451-3456, Journal of clinical endocrinology & metabolism
— id: 845172, year: 2006, vol: 91, page: 3451, stat: Journal Article,

Bisphosphonate treatment of pediatric bone disease
Speiser, Phyllis W; Clarson, Cheril L; Eugster, Erica A; Kemp, Stephen F; Radovick, Sally; Rogol, Alan D; Wilson, Thomas A
2005 Dec;3(2):87-96, Pediatric endocrinology reviews : PER
— id: 63069, year: 2005, vol: 3, page: 87, stat: Journal Article,

Childhood obesity
Speiser, Phyllis W; Rudolf, Mary C J; Anhalt, Henry; Camacho-Hubner, Cecilia; Chiarelli, Francesco; Eliakim, Alon; Freemark, Michael; Gruters, Annette; Hershkovitz, Eli; Iughetti, Lorenzo; Krude, Heiko; Latzer, Yael; Lustig, Robert H; Pescovitz, Ora Hirsch; Pinhas-Hamiel, Orit; Rogol, Alan D; Shalitin, Shlomit; Sultan, Charles; Stein, Daniel; Vardi, Pnina; Werther, George A; Zadik, Zvi; Zuckerman-Levin, Nehama; Hochberg, Zeev
2005 Mar;90(3):1871-1887, Journal of clinical endocrinology & metabolism
— id: 94841, year: 2005, vol: 90, page: 1871, stat: Journal Article,

Urinary meprin-alpha: a potential marker of diabetic nephropathy
DeGuzman, Jocelyn B; Speiser, Phyllis W; Trachtman, Howard
2004 Dec;17(12):1663-1666, Journal of pediatric endocrinology & metabolism
— id: 94840, year: 2004, vol: 17, page: 1663, stat: Journal Article,

Safety of medications and hormones used in pediatric endocrinology: adrenal
Frank, Graeme R; Speiser, Phyllis W; Griffin, Kurt J; Stratakis, Constantine A
2004 Nov;2 Suppl 1:134-145, Pediatric endocrinology reviews : PER
— id: 62647, year: 2004, vol: 2 Suppl 1, page: 134, stat: Journal Article,

Improving neonatal screening for congenital adrenal hyperplasia
Speiser, Phyllis W
2004 Aug;89(8):3685-3686, Journal of clinical endocrinology & metabolism
— id: 94842, year: 2004, vol: 89, page: 3685, stat: Journal Article,

Congenital adrenal hyperplasia
Speiser, Phyllis W; White, Perrin C
2003 Aug 21;349(8):776-788, New England journal of medicine
— id: 94843, year: 2003, vol: 349, page: 776, stat: Journal Article,

New therapies for congenital adrenal hyperplasia
Speiser, PW
2003 ;10(1):32-36, Current opinion in endocrinology & diabetes
— id: 651802, year: 2003, vol: 10, page: 32, stat: Journal Article,

Update of guidelines for the use of growth hormone in children: the Lawson Wilkins Pediatric Endocrinology Society Drug and Therapeutics Committee
Wilson, Thomas A; Rose, Susan R; Cohen, Pinchas; Rogol, Alan D; Backeljauw, Philippe; Brown, Rosalind; Hardin, Dana S; Kemp, Stephen F; Lawson, Margaret; Radovick, Sally; Rosenthal, Stephen M; Silverman, Lawrence; Speiser, Phyllis
2003 Oct;143(4):415-421, Journal of pediatrics
— id: 845092, year: 2003, vol: 143, page: 415, stat: Journal Article,

Successful computerization of a hospital-based pediatric endocrinology practice
Brenner, DJ; Carey, DE; Fort, P; Frank, GR; Kreitzer, PM; Speiser, PW
2002 Apr;51(4):685-, Pediatric research
— id: 27463, year: 2002, vol: 51, page: 685, stat: Journal Article,

Consensus statement on 21-hydroxylase deficiency from the European Society for Paediatric Endocrinology and the Lawson Wilkins Pediatric Endocrine Society
Clayton, Peter E; Miller, Walter L; Oberfield, Sharon E; Ritzen, E Martin; Sippell, Wolfgang G; Speiser, Phyllis W
2002 ;58(4):188-195, Hormone research
— id: 94844, year: 2002, vol: 58, page: 188, stat: Journal Article,

Adrenomedullary function may predict phenotype and genotype in classic 21-hydroxylase deficiency
Speiser, Phyllis W
2002 Jul;87(7):3029-3030, Journal of clinical endocrinology & metabolism
— id: 94847, year: 2002, vol: 87, page: 3029, stat: Journal Article,

Continuous glucose monitoring in managing diabetes in children
Speiser, Phyllis W
2002 Jul-Aug;18(4):330-331, Diabetes/metabolism research & reviews
— id: 94845, year: 2002, vol: 18, page: 330, stat: Journal Article,

Impaired glucose tolerance in obese children and adolescents
Speiser, Phyllis W
2002 Jul 25;347(4):290-2; author reply 290, New England journal of medicine
— id: 94846, year: 2002, vol: 347, page: 290, stat: Journal Article,

Long-term consequences of childhood-onset congenital adrenal hyperplasia
White, Perrin C; Speiser, Phyllis W
2002 Jun;16(2):273-288, Best practice & research. Clinical endocrinology & metabolism
— id: 94848, year: 2002, vol: 16, page: 273, stat: Journal Article,

Profiles of obese children presenting for metabolic evaluation
Anavian J; Brenner DJ; Fort P; Speiser PW
2001 Sep-Oct;14(8):1145-1150, Journal of pediatric endocrinology & metabolism
— id: 39477, year: 2001, vol: 14, page: 1145, stat: Journal Article,

Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency
Speiser, P W
2001 Mar;30(1):31-59, vi, Endocrinology & metabolism clinics of North America
— id: 845112, year: 2001, vol: 30, page: 31, stat: Journal Article,

Congenital adrenal hyperplasia: transition from chil dhood to adulthood
Speiser, P W
2001 Oct;24(9):681-691, Journal of endocrinological investigation
— id: 845122, year: 2001, vol: 24, page: 681, stat: Journal Article,

Molecular diagnosis of CYP21 mutations in congenital adrenal hyperplasia: implications for genetic counseling
Speiser, P W
2001 ;1(2):101-110, American journal of pharmacogenomics
— id: 845142, year: 2001, vol: 1, page: 101, stat: Journal Article,

Profile of obese children presenting for metabolic evaluation
Anavian, J; Fort, P; Speiser, PW
2000 APR ;47(4):123A-123A, Pediatric research
— id: 54673, year: 2000, vol: 47, page: 123A, stat: Journal Article,

Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype
Bellus, G A; Spector, E B; Speiser, P W; Weaver, C A; Garber, A T; Bryke, C R; Israel, J; Rosengren, S S; Webster, M K; Donoghue, D J; Francomano, C A
2000 Dec;67(6):1411-1421, American journal of human genetics
— id: 845132, year: 2000, vol: 67, page: 1411, stat: Journal Article,

[Molecular analysis of] Combined 21-hydroxylase and 11beta-hydroxylase deficiency: patient report and molecular basis [In Process Citation]
Gillis D; Speiser P; Zhou Z; Rosler A
2000 Jul-Aug;13(7):945-949, Journal of pediatric endocrinology & metabolism
— id: 9077, year: 2000, vol: 13, page: 945, stat: Journal Article,

21-Hydroxylase-deficient nonclassic adrenal hyperplasia is a progressive disorder: a multicenter study
Moran, C; Azziz, R; Carmina, E; Dewailly, D; Fruzzetti, F; Ibanez, L; Knochenhauer, E S; Marcondes, J A; Mendonca, B B; Pignatelli, D; Pugeat, M; Rohmer, V; Speiser, P W; Witchel, S F
2000 Dec;183(6):1468-1474, American journal of obstetrics & gynecology
— id: 845102, year: 2000, vol: 183, page: 1468, stat: Journal Article,

Ovarian hyperthecosis in the setting of portal hypertension
Speiser PW; Susin M; Sasano H; Bohrer S; Markowitz J
2000 Feb;85(2):873-877, Journal of clinical endocrinology & metabolism
— id: 9032, year: 2000, vol: 85, page: 873, stat: Journal Article,

A multicenter study of women with nonclassical congenital adrenal hyperplasia: relationship between genotype and phenotype
Speiser, P W; Knochenhauer, E S; Dewailly, D; Fruzzetti, F; Marcondes, J A; Azziz, R
2000 Nov;71(3):527-534, Molecular genetics & metabolism
— id: 845152, year: 2000, vol: 71, page: 527, stat: Journal Article,

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency [In Process Citation]
White PC; Speiser PW
2000 Jun;21(3):245-291, Endocrine reviews
— id: 9031, year: 2000, vol: 21, page: 245, stat: Journal Article,

Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature review
Damore ME; Speiser PW; Slonim AE; New MI; Shanske S; Xia W; Santorelli FM; DiMauro S
1999 Mar-Apr;12(2):207-213, Journal of pediatric endocrinology & metabolism
— id: 9036, year: 1999, vol: 12, page: 207, stat: Journal Article,

Genotyping of CYP21, linked chromosome 6p markers, and a sex-specific gene in neonatal screening for congenital adrenal hyperplasia
Fitness J; Dixit N; Webster D; Torresani T; Pergolizzi R; Speiser PW; Day DJ
1999 Mar;84(3):960-966, Journal of clinical endocrinology & metabolism
— id: 9037, year: 1999, vol: 84, page: 960, stat: Journal Article,

Prenatal treatment of congenital adrenal hyperplasia
Speiser PW
1999 Aug;162(2):534-536, Journal of urology
— id: 9035, year: 1999, vol: 162, page: 534, stat: Journal Article,

Toward better treatment of congenital adrenal hyperplasia
Speiser PW
1999 Sep;51(3):273-274, Clinical endocrinology
— id: 9034, year: 1999, vol: 51, page: 273, stat: Journal Article,

Regulation of HSD17B1 and SRD5A1 in lymphocytes
Zhou Z; Speiser PW
1999 Nov;68(3):410-417, Molecular genetics & metabolism
— id: 9033, year: 1999, vol: 68, page: 410, stat: Journal Article,

Study of a kindred with classic congenital adrenal hyperplasia: diagnostic challenge due to phenotypic variance
Chin D; Speiser PW; Imperato-McGinley J; Dixit N; Uli N; David R; Oberfield SE
1998 Jun;83(6):1940-1945, Journal of clinical endocrinology & metabolism
— id: 7941, year: 1998, vol: 83, page: 1940, stat: Journal Article,

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency
Speiser PW; White PC
1998 Oct;49(4):411-417, Clinical endocrinology
— id: 7453, year: 1998, vol: 49, page: 411, stat: Journal Article,

Prominent sex steroid metabolism in human lymphocytes
Zhou Z; Shackleton CH; Pahwa S; White PC; Speiser PW
1998 Mar 16;138(1-2):61-69, Molecular & cellular endocrinology
— id: 9038, year: 1998, vol: 138, page: 61, stat: Journal Article,

Expression of myogenic regulatory factors in normal and dystrophic mice: effects of IGF-1 treatment
Hsu HH; Zdanowicz MM; Agarwal VR; Speiser PW
1997 Apr;60(2):142-148, Biochemical & molecular medicine
— id: 9040, year: 1997, vol: 60, page: 142, stat: Journal Article,

Magnetic resonance imaging in the congenital adrenal hyperplasia population: increased frequency of white-matter abnormalities and temporal lobe atrophy
Nass R; Heier L; Moshang T; Oberfield S; George A; New MI; Speiser PW
1997 Apr;12(3):181-186, Journal of child neurology
— id: 7224, year: 1997, vol: 12, page: 181, stat: Journal Article,

Steroid 21-hydroxylase expression and activity in human lymphocytes
Zhou Z; Agarwal VR; Dixit N; White P; Speiser PW
1997 Mar 14;127(1):11-18, Molecular & cellular endocrinology
— id: 9041, year: 1997, vol: 127, page: 11, stat: Journal Article,

Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigrees
Day DJ; Speiser PW; Schulze E; Bettendorf M; Fitness J; Barany F; White PC
1996 Dec;5(12):2039-2048, Human molecular genetics
— id: 9042, year: 1996, vol: 5, page: 2039, stat: Journal Article,

Detection of steroid 21-hydroxylase alleles using gene-specific PCR and a multiplexed ligation detection reaction
Day DJ; Speiser PW; White PC; Barany F
1995 Sep 1;29(1):152-162, Genomics
— id: 9044, year: 1995, vol: 29, page: 152, stat: Journal Article,

Splicing mutation in CYP21 associated with delayed presentation of salt-wasting congenital adrenal hyperplasia
Kohn B; Day D; Alemzadeh R; Enerio D; Patel SV; Pelczar JV; Speiser PW
1995 Jul 3;57(3):450-454, American journal of medical genetics
— id: 9045, year: 1995, vol: 57, page: 450, stat: Journal Article,

Transient central precocious puberty in non-classic 21-hydroxylase deficiency
Speiser PW
1995 Oct-Dec;8(4):287-289, Journal of pediatric endocrinology & metabolism
— id: 9043, year: 1995, vol: 8, page: 287, stat: Journal Article,

Failure of steroid replacement to consistently normalize pituitary function in congenital adrenal hyperplasia: hormonal and MRI data
Speiser PW; Heier L; Serrat J; New MI; Nass R
1995 ;44(6):241-246, Hormone research
— id: 6966, year: 1995, vol: 44, page: 241, stat: Journal Article,

Prenatal diagnosis and management of congenital adrenal hyperplasia
Speiser PW; New MI
1994 Sep;21(3):631-645, Clinics in perinatology
— id: 9046, year: 1994, vol: 21, page: 631, stat: Journal Article,

Prenatal diagnosis and treatment of congenital adrenal hyperplasia
Speiser PW; New MI
1994 Jul-Sep;7(3):183-191, Journal of pediatric endocrinology & metabolism
— id: 9047, year: 1994, vol: 7, page: 183, stat: Journal Article,

Molecular genetic prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization
Speiser PW; White PC; Dupont J; Zhu D; Mercado A; New MI
1994 ;49:367-371, Recent progress in hormone research
— id: 9050, year: 1994, vol: 49, page: 367, stat: Journal Article,

Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blot
Speiser PW; White PC; Dupont J; Zhu D; Mercado AB; New MI
1994 Apr;93(4):424-428, Human genetics
— id: 9049, year: 1994, vol: 93, page: 424, stat: Journal Article,

Steroid 11 beta-hydroxylase deficiency and related disorders
White PC; Speiser PW
1994 Jun;23(2):325-339, Endocrinology & metabolism clinics of North America
— id: 9048, year: 1994, vol: 23, page: 325, stat: Journal Article,

Mutations in steroid 21-hydroxylase (CYP21)
White PC; Tusie-Luna MT; New MI; Speiser PW
1994 ;3(4):373-378, Human mutation
— id: 9051, year: 1994, vol: 3, page: 373, stat: Journal Article,

Mutations in the CYP11B1 gene causing congenital adrenal hyperplasia and hypertension cluster in exons 6, 7, and 8
Curnow KM; Slutsker L; Vitek J; Cole T; Speiser PW; New MI; White PC; Pascoe L
1993 May 15;90(10):4552-4556, Proceedings of the National Academy of Sciences of the United States of America
— id: 9053, year: 1993, vol: 90, page: 4552, stat: Journal Article,

Investigation of the mechanism of hypertension in apparent mineralocorticoid excess
Speiser PW; Riddick LM; Martin K; New MI
1993 Jul;42(7):843-845, Metabolism clinical & experimental
— id: 9052, year: 1993, vol: 42, page: 843, stat: Journal Article,

Prenatal diagnosis/treatment in families at risk for infants with steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia)
Karaviti LP; Mercado AB; Mercado MB; Speiser PW; Buegeleisen M; Crawford C; Antonian L; White PC; New MI
1992 Mar;41(3-8):445-451, Journal of steroid biochemistry & molecular biology
— id: 9058, year: 1992, vol: 41, page: 445, stat: Journal Article,

Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2
Pascoe L; Curnow KM; Slutsker L; Connell JM; Speiser PW; New MI; White PC
1992 Sep 1;89(17):8327-8331, Proceedings of the National Academy of Sciences of the United States of America
— id: 9055, year: 1992, vol: 89, page: 8327, stat: Journal Article,

Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Speiser PW; Dupont J; Zhu D; Serrat J; Buegeleisen M; Tusie-Luna MT; Lesser M; New MI; White PC
1992 Aug;90(2):584-595, Journal of clinical investigation
— id: 9056, year: 1992, vol: 90, page: 584, stat: Journal Article,

Genotype of Yupik Eskimos with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Speiser PW; New MI; Tannin GM; Pickering D; Yang SY; White PC
1992 Mar;88(6):647-648, Human genetics
— id: 9059, year: 1992, vol: 88, page: 647, stat: Journal Article,

Insulin insensitivity in adrenal hyperplasia due to nonclassical steroid 21-hydroxylase deficiency
Speiser PW; Serrat J; New MI; Gertner JM
1992 Dec;75(6):1421-1424, Journal of clinical endocrinology & metabolism
— id: 9054, year: 1992, vol: 75, page: 1421, stat: Journal Article,

Polymorphism in the RD (D6S45) gene
White PC; Vitek J; Lahita RG; Speiser PW
1992 May;89(2):243-244, Human genetics
— id: 9057, year: 1992, vol: 89, page: 243, stat: Journal Article,

Aldosterone synthesis in salt-wasting congenital adrenal hyperplasia with complete absence of adrenal 21-hydroxylase
Speiser PW; Agdere L; Ueshiba H; White PC; New MI
1991 Jan 17;324(3):145-149, New England journal of medicine
— id: 9061, year: 1991, vol: 324, page: 145, stat: Journal Article,

A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele
Tusie-Luna MT; Speiser PW; Dumic M; New MI; White PC
1991 May;5(5):685-692, Molecular endocrinology
— id: 9060, year: 1991, vol: 5, page: 685, stat: Journal Article,

An update on the frequency of nonclassic deficiency of adrenal 21-hydroxylase in the Yugoslav population
Dumic M; Brkljacic L; Speiser PW; Wood E; Crawford C; Plavsic V; Baniceviac M; Radmanovic S; Radica A; Kastelan A; et al
1990 Jun;122(6):703-710, Acta endocrinologica (Copenhagen)
— id: 9062, year: 1990, vol: 122, page: 703, stat: Journal Article,

First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)
Speiser PW; Laforgia N; Kato K; Pareira J; Khan R; Yang SY; Whorwood C; White PC; Elias S; Schriock E; et al
1990 Apr;70(4):838-848, Journal of clinical endocrinology & metabolism
— id: 9064, year: 1990, vol: 70, page: 838, stat: Journal Article,

Prevalence of nonclassical steroid 21-hydroxylase deficiency based on a morning salivary 17-hydroxyprogesterone screening test: a small sample study
Zerah M; Ueshiba H; Wood E; Speiser PW; Crawford C; McDonald T; Pareira J; Gruen D; New MI
1990 Jun;70(6):1662-1667, Journal of clinical endocrinology & metabolism
— id: 9063, year: 1990, vol: 70, page: 1662, stat: Journal Article,

Growth and final height in classical and nonclassical 21-hydroxylase deficiency
New MI; Gertner JM; Speiser PW; Del Balzo P
1989 ;12(8 Suppl 3):91-95, Journal of endocrinological investigation
— id: 9066, year: 1989, vol: 12, page: 91, stat: Journal Article,

Clinical and genetic characterization of nonclassic 21-hydroxylase deficiency
Speiser PW; New MI; White PC
1989 ;15(1-2):257-276, Endocrine research
— id: 9067, year: 1989, vol: 15, page: 257, stat: Journal Article,

Structure of the human RD gene: a highly conserved gene in the class III region of the major histocompatibility complex
Speiser PW; White PC
1989 Dec;8(10):745-751, DNA
— id: 9065, year: 1989, vol: 8, page: 745, stat: Journal Article,

Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequencies
Aston CE; Sherman SL; Morton NE; Speiser PW; New MI
1988 Sep;43(3):304-310, American journal of human genetics
— id: 9068, year: 1988, vol: 43, page: 304, stat: Journal Article,

Growth and final height in classical and nonclassical 21-hydroxylase deficiency
New MI; Gertner JM; Speiser PW; del Balzo P
1988 ;30 Suppl:79-88, Acta paediatrica japonica
— id: 9071, year: 1988, vol: 30 Suppl, page: 79, stat: Journal Article,

A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiency
Sherman SL; Aston CE; Morton NE; Speiser PW; New MI
1988 Jun;42(6):830-838, American journal of human genetics
— id: 9070, year: 1988, vol: 42, page: 830, stat: Journal Article,

Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1
Speiser PW; New MI; White PC
1988 Jul 7;319(1):19-23, New England journal of medicine
— id: 9069, year: 1988, vol: 319, page: 19, stat: Journal Article,

Genotype and hormonal phenotype in nonclassical 21-hydroxylase deficiency
Speiser PW; New MI
1987 Jan;64(1):86-91, Journal of clinical endocrinology & metabolism
— id: 9072, year: 1987, vol: 64, page: 86, stat: Journal Article,

Genetics of adrenal steroid 21-hydroxylase deficiency
New MI; Speiser PW
1986 Aug;7(3):331-349, Endocrine reviews
— id: 9073, year: 1986, vol: 7, page: 331, stat: Journal Article,

Pseudohypoaldosteronism: a review and report of two new cases
Speiser PW; Stoner E; New MI
1986 ;196:173-195, Advances in experimental medicine & biology
— id: 9074, year: 1986, vol: 196, page: 173, stat: Journal Article,

High frequency of nonclassical steroid 21-hydroxylase deficiency
Speiser PW; Dupont B; Rubinstein P; Piazza A; Kastelan A; New MI
1985 Jul;37(4):650-667, American journal of human genetics
— id: 9039, year: 1985, vol: 37, page: 650, stat: Journal Article,

Excess mineralocorticoid receptor activity in patients with dexamethasone-suppressible hyperaldosteronism is under adrenocorticotropin control
Speiser PW; Martin KO; Kao-Lo G; New MI
1985 Aug;61(2):297-302, Journal of clinical endocrinology & metabolism
— id: 9075, year: 1985, vol: 61, page: 297, stat: Journal Article,