Speiser, Phyllis: search on Z-Library

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1

Premature Adrenarche

Novello, Laura, Speiser, Phyllis W.

Journal:

Pediatric Annals

Year:

2018

Language:

english

File:

PDF, 1.05 MB

english, 2018

2

Psychosocial Screening in Disorders/Differences of Sex Development: Psychometric Evaluation of the Psychosocial Assessment Tool

Ernst, Michelle M., Gardner, Melissa, Mara, Constance A., Délot, Emmanuèle C., Fechner, Patricia Y., Fox, Michelle, Rutter, Meilan M., Speiser, Phyllis W., Vilain, Eric, Weidler, Erica M., Sandberg, D

Journal:

Hormone Research in Paediatrics

Year:

2019

Language:

english

File:

PDF, 289 KB

english, 2019

3

Congenital Adrenal Hyperplasia

Donohoue, Patricia A., Poth, Merrily, Speiser, Phyllis W.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2010

Language:

english

File:

PDF, 39 KB

english, 2010

4

CONGENITAL ADRENAL HYPERPLASIA OWING TO 21-HYDROXYLASE DEFICIENCY

Speiser, Phyllis W.

Journal:

Endocrinology and Metabolism Clinics of North America

Year:

2001

Language:

english

File:

PDF, 1.48 MB

english, 2001

5

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, H

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2005

Language:

english

File:

PDF, 158 KB

english, 2005

6

PREFACE

SPEISER, PHYLLIS W.

Journal:

Endocrinology and Metabolism Clinics of North America

Year:

2001

Language:

english

File:

PDF, 210 KB

english, 2001

7

Treatment Outcomes in Congenital Adrenal Hyperplasia

Cheng, Tina Q., Speiser, Phyllis W.

Journal:

Advances in Pediatrics

Year:

2012

Language:

english

File:

PDF, 231 KB

english, 2012

8

A Multicenter Study of Women with Nonclassical Congenital Adrenal Hyperplasia: Relationship between Genotype and Phenotype

Phyllis W. Speiser, Eric S. Knochenhauer, Didier Dewailly, Franca Fruzzetti, Jose A.M. Marcondes, Ricardo Azziz

Journal:

Molecular Genetics and Metabolism

Year:

2000

Language:

english

File:

PDF, 63 KB

english, 2000

9

New therapies for congenital adrenal hyperplasia

Speiser, Phyllis W.

Journal:

Current Opinion in Endocrinology & Diabetes

Year:

2003

Language:

english

File:

PDF, 253 KB

english, 2003

10

Congenital adrenal hyperplasia: an update in children

Trapp, Christine M, Speiser, Phyllis W, Oberfield, Sharon E

Journal:

Current Opinion in Endocrinology Diabetes and Obesity

Year:

2011

Language:

english

File:

PDF, 133 KB

english, 2011

11

The Hormone Foundation’s Patient Guide to Congenital Adrenal Hyperplasia

Oberfield, Sharon E., Speiser, Phyllis W.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2010

Language:

english

File:

PDF, 73 KB

english, 2010

12

Congenital adrenal hyperplasia: Transition from childhood to adulthood

Speiser, Phyllis W.

Journal:

Journal of Endocrinological Investigation

Year:

2001

Language:

english

File:

PDF, 105 KB

english, 2001

13

Genetics of Adrenal Steroid 21-Hydroxylase Deficiency*

NEW, MARIA I., SPEISER, PHYLLIS W.

Journal:

Endocrine Reviews

Year:

1986

Language:

english

File:

PDF, 2.81 MB

english, 1986

14

Ovarian Hyperthecosis in the Setting of Portal Hypertension

Speiser, Phyllis W., Susin, Myron, Sasano, Hironobu, Bohrer, Stuart, Markowitz, James

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2000

Language:

english

File:

PDF, 1.15 MB

english, 2000

15

ATYPICAL 11β-HYDROXYLASE DEFICIENCY: ABSENCE OF RENIN SUPPRESSION AND HYPERTENSION DESPITE HIGH DOC

Speiser, Phyllis W, Neirery, Robin L, Chow, Diane, Martin, Kumiko O, New, Maria I

Journal:

Pediatric Research

Year:

1987

Language:

english

File:

PDF, 175 KB

english, 1987

16

Steroid 21-hydroxylase expression and activity in human lymphocytes

Zhifeng Zhou, Veena R Agarwal, Naznin Dixit, Perrin White, Phyllis W Speiser

Journal:

Molecular and Cellular Endocrinology

Year:

1997

Language:

english

File:

PDF, 388 KB

english, 1997

17

Failure of Steroid Replacement to Consistently Normalize Pituitary Function in Congenital Adrenal Hyperplasia: Hormonal and MRI Data

Speiser, Phyllis W., Heier, Linda, Serrat, Jorge, New, Maria I., Nass, Ruth

Journal:

Hormone Research

Year:

1995

File:

PDF, 1.21 MB

1995

18

Transient Central Precocious Puberty in Non-Classic 21-Hydroxylase Deficiency

Speiser, Phyllis W.

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

1995

Language:

english

File:

PDF, 420 KB

english, 1995

19

Excess Mineralocorticoid Receptor Activity in Patients with Dexamethasone-Suppressible Hyperaldosteronism Is under Adrenocorticotropin Control*

SPEISER, PHYLLIS W., MARTIN, KUMIKO O., KAO-LO, GRACE, NEW, MARIA I.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

1985

Language:

english

File:

PDF, 616 KB

english, 1985

20

Congenital adrenal hyperplasia

Speiser, Phyllis W, White, Perrin C, New, Maria I

Journal:

Reproductive Medicine Review

Year:

1993

Language:

english

File:

PDF, 1.09 MB

english, 1993

21

Investigation of the mechanism of hypertension in apparent mineralocorticoid excess

Phyllis W. Speiser, Linda M. Riddick, Kumiko Martin, Maria I. New

Journal:

Year:

1993

Language:

english

File:

PDF, 413 KB

english, 1993

22

Managing Childhood Overweight: Behavior, Family, Pharmacology, and Bariatric Surgery Interventions

Yael Latzer, Laurel Edmunds, Silvana Fenig, Moria Golan, Eitan Gur, Ze'ev Hochberg, Diane Levin-Zamir, Eynat Zubery, Phyllis W. Speiser, Daniel Stein

Journal:

Year:

2009

Language:

english

File:

PDF, 774 KB

english, 2009

23

Long-term consequences of childhood-onset congenital adrenal hyperplasia

Perrin C. White, Phyllis W. Speiser

Journal:

Best Practice & Research Clinical Endocrinology & Metabolism

Year:

2002

Language:

english

File:

PDF, 179 KB

english, 2002

24

High Frequency of Nonclassical Steroid 21-Hydroxylase Deficiency

SPEISER, PHYLLIS W., DUPONT, B O, RUBINSTEIN, PABLO, PIAZZA, ALBERTO, KASTELAN, ANDRIJA, NEW, MARIA I.

Journal:

Obstetric and Gynecologic Survey

Year:

1986

File:

PDF, 247 KB

1986

25

Adrenal Incidentalomas

Nieman, Lynnette, Speiser, Phyllis, Young, William F.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2013

Language:

english

File:

PDF, 685 KB

english, 2013

26

Cardiovascular and Metabolic Outcomes in Congenital Adrenal Hyperplasia: A Systematic Review and Meta-Analysis

Tamhane, Shrikant, Rodriguez-Gutierrez, Rene, Iqbal, Anoop Mohamed, Prokop, Larry J, Bancos, Irina, Speiser, Phyllis W, Murad, Mohammad Hassan

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2018

Language:

english

File:

PDF, 269 KB

english, 2018

27

Genetics of steroid 21-hydroxylase deficiency

Phyllis W. Speiser, Maria I. New

Journal:

Trends in Genetics

Year:

1985

Language:

english

File:

PDF, 426 KB

english, 1985

28

Novel P450c17 Mutation H373D Causing Combined 17α-Hydroxylase/17,20-Lyase Deficiency

Sahakitrungruang, Taninee, Tee, Meng Kian, Speiser, Phyllis W., Miller, Walter L.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2009

Language:

english

File:

PDF, 101 KB

english, 2009

29

The Genetics of Steroid 21-Hydroxylase Deficiency

Speiser, Phyllis W.

Journal:

The Endocrinologist

Year:

2005

Language:

english

File:

PDF, 317 KB

english, 2005

30

Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society* Clinical Practice Guideline

Speiser, Phyllis W, Arlt, Wiebke, Auchus, Richard J, Baskin, Laurence S, Conway, Gerard S, Merke, Deborah P, Meyer-Bahlburg, Heino F L, Miller, Walter L, Murad, M Hassan, Oberfield, Sharon E, White, P

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2018

Language:

english

File:

PDF, 2.05 MB

english, 2018

31

SUN-159 17-beta Hydroxysteroid Dehydrogenase 3 Deficiency in 1 Month Old Infant

Mathew, Deepa, Speiser, Phyllis Witzel, Panayiotopoulos, Aristotle, Pisani, Laura

Journal:

Journal of the Endocrine Society

Year:

2020

File:

PDF, 90 KB

2020

32

Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blot

Phyllis W. Speiser, Perrin C. White, Jacob Dupont, Deguang Zhu, Arlene B. Mercado, Maria I. New

Journal:

Year:

1994

Language:

english

File:

PDF, 593 KB

english, 1994

33

Genotype of Yupik Eskimos with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Phyllis W. Speisere, Maria I. New, Grace M. Tannin, Donald Pickering, Soo Young Yang, Perrin C. White

Journal:

Year:

1992

Language:

english

File:

PDF, 266 KB

english, 1992

34

A Mutation (Pro-30 to Leu) in CYP 21 Represents a Potential Nonclassic Steroid 21-Hydroxylase Deficiency Allele

Tusie-Luna, Maria-Teresa, Speiser, Phyllis W., Dumic, Miro, New, Maria I., White, Perrin C.

Journal:

Molecular Endocrinology

Year:

1991

Language:

english

File:

PDF, 899 KB

english, 1991

35

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.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2008

Language:

english

File:

PDF, 287 KB

english, 2008

36

Genotyping of CYP21, Linked Chromosome 6p Markers, and a Sex-Specific Gene in Neonatal Screening for Congenital Adrenal Hyperplasia 1

Fitness, Jodene, Dixit, Naznin, Webster, Dianne, Torresani, Toni, Pergolizzi, Robert, Speiser, Phyllis W., Day, Darren J.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

1999

Language:

english

File:

PDF, 115 KB

english, 1999

37

Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency 1

White, Perrin C., Speiser, Phyllis W.

Journal:

Endocrine Reviews

Year:

2000

Language:

english

File:

PDF, 809 KB

english, 2000

38

Molecular Genetic Analysis of Nonclassic Steroid 21 -Hydroxylase Deficiency Associated with HLA-B14, DRI

SPEISER, PHYLLIS W., NEW, MARIA I., WHITE, PERRIN C.

Journal:

Obstetric and Gynecologic Survey

Year:

1988

File:

PDF, 244 KB

1988

39

Bilateral Adrenal Uptake of Gallium-67 Citrate in a Patient with Congenital Adrenal Hyperplasia

LORBERBOYM, MORDECHAI, SARKAR, SAUL D., SPEISER, PHYLLIS, TANNEN, GRACE, NEW, MARIA I.

Journal:

Clinical Nuclear Medicine

Year:

1990

File:

PDF, 85 KB

1990

40

Molecular Diagnosis ofCYP21Mutations in Congenital Adrenal Hyperplasia

Dr Phyllis W. Speiser

Journal:

American Journal of PharmacoGenomics

Year:

2001

Language:

english

File:

PDF, 163 KB

english, 2001

41

Authors’ Response: Regarding the Consensus Statement on 21-Hydroxylase Deficiency from the Lawson Wilkins Pediatric Endocrine Society and The European Society for Paediatric Endocrinology

Miller, Walter L., Oberfield, Sharon E., Speiser, Phyllis W., Baskin, Laurence S., Donahoe, Patricia K., N-Fekete, Claire, Hutson, John M., Poppas, Dix Phillip

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2003

Language:

english

File:

PDF, 93 KB

english, 2003

42

A Phase 2, Multicenter Study of Nevanimibe for the Treatment of Congenital Adrenal Hyperplasia

Speiser, Phyllis W

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2020

File:

PDF, 295 KB

2020

43

Continuous glucose monitoring in managing diabetes in children

Phyllis W. Speiser

Journal:

Diabetes/Metabolism Research and Reviews

Year:

2002

Language:

english

File:

PDF, 39 KB

english, 2002

44

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

Phyllis W. Speiser, Perrin C. White

Journal:

Clinical Endocrinology

Year:

1998

Language:

english

File:

PDF, 332 KB

english, 1998

45

Prevalence of Nonclassical Steroid 21-Hydroxylase Deficiency Based on a Morning Salivary 17-hydroxyprogesterone Screening Test: A Small Sample Study*

ZERAH, MICHELE, UESHIBA, HAJIME, WOOD, ELIZABETH, SPEISER, PHYLLIS W., CRAWFORD, CHRISTOPHER, MCDONALD, TOBEY, PAREIRA, JUDITH, GRUEN, DAVID, NEW, MARIA I.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

1990

Language:

english

File:

PDF, 883 KB

english, 1990

46

Glucocorticoid-Suppressible Hyperaldosteronism Results from Hybrid Genes Created by Unequal Crossovers between CYP11B1 and CYP11B2

Leigh Pascoe, Kathleen M. Curnow, Liliya Slutsker, John M. C. Connell, Phyllis W. Speiser, Maria I. New and Perrin C. White

Journal:

Proceedings of the National Academy of Sciences

Year:

1992

Language:

english

File:

PDF, 1.11 MB

english, 1992

47

The Reduce Obesity and Diabetes (ROAD) Project: Design and Methodological Considerations

Rosenbaum, Michael, Accacha, Siham D., Altshuler, Lisa A., Carey, Dennis E., Fennoy, Ilene, Lowell, Barbara C., Rapaport, Robert, Speiser, Phyllis W., Shelov, Steven P.

Journal:

Childhood Obesity (Formerly Obesity and Weight Management)

Year:

2011

Language:

english

File:

PDF, 1.32 MB

english, 2011

48

Genetic Steroid Disorders || Debates and Controversies in Genetic Steroid Disorders

Speiser, Phyllis W.

Year:

2014

Language:

english

File:

PDF, 200 KB

english, 2014

49

Growth and development: Congenital adrenal hyperplasia—glucocorticoids and height

Speiser, Phyllis W.

Journal:

Nature Reviews Endocrinology (formerly Nature Clinical Practice Endocrinology & Metabolism)

Year:

2010

Language:

english

File:

PDF, 132 KB

english, 2010

50

Genotype and Hormonal Phenotype in Nonclassical 21-Hydroxylase Deficiency*

SPEISER, PHYLLIS W., NEW, MARIA I.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

1987

Language:

english

File:

PDF, 754 KB

english, 1987

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