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Genetic steroid disorders

Author: Maria I NewOksana LekarevAlan ParsaTony T YuenBert W O'MalleyAll authors
Publisher: London : Academic Press, 2014.
Edition/Format:   eBook : Document : EnglishView all editions and formats
Summary:
This is a comprehensive book addressing steroid disorders from hormonal, genetic, psychological, and surgical perspectives.
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Genre/Form: Electronic books
Additional Physical Format: Print version:
Genetic steroid disorders.
London : Academic Press, 2014
(DLC) 2012276103
Material Type: Document, Internet resource
Document Type: Internet Resource, Computer File
All Authors / Contributors: Maria I New; Oksana Lekarev; Alan Parsa; Tony T Yuen; Bert W O'Malley; Gary D Hammer
ISBN: 9780123914675 0123914671
OCLC Number: 880437553
Description: 1 online resource (xiii, 392 pages, 16 unnumbered pages of plates) : illustrations (some color), maps
Contents: 1. Introduction / Maria I. New --
2. Adrenal development / Yewei Xing, John C. Achermann, Gary D. Hammer --
3A. Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency / Maria I. New, Oksana Lekarev, Denesy Mancenido, Alan Parsa, Tony Yuen --
3B. The history of prenatal diagnosis of congenital adrenal hyperplasia / Denesy Mancenido, Maria I. New --
3C. Growth hormone therapy to improve adult height in patients with congenital adrenal hyperplasia / Karen Lin-Su, Oksana Lekarev, Maria I. New --
3D. Steroid 11B-hydroxylase deficiency and related disorders / Perrin C. White --
3E. Ambiguous genitalia in newborns / Sowmya Krishnan, Amy B. Wisniewski --
3F. 3B-hydroxysteroid dehydrogenase deficiency / Yves Morel, Florence Roucher, Ingrid Plotton, Jacques Simard, Mauricio Coll --
3G. Genetic deficiencies of cytochrome P450c17 (CYP17A1) : combined 17-hydroxylase/17,20-lyase deficiency and isolated 17,20-lyase deficiency / Richard J. Auchus --
3H. P450 oxidoreductase deficiency (PORD) / Christa E. Fluck, Amit V. Pandey --
3I. Disorders in the initial steps in steroidogenesis / Walter L. Miller, Zoran S. Gucev --
3J. Aromatase deficiency and aromatase excess / Jonathan F. Russell, Jenise C. Wong, Melvin M. Grumbach --
3K. 46,XY DSD due to 17B-hydroxysteroid dehydrogenase 3 deficiency / Berenice B. Mendonca, Elaine M.F. Costa, Marlene Inacio, Ari A. Oliveira Junior, Regina M. Martin, Mirian Y. Nishi, Aline Z. Machado, Filomena Marino Carvalho, Francisco Denes Tibor, Sorahia Domenice --
4A. Steroid 5a-reductase 2 deficiency / David W. Russell, Jean D. Wilson --
4B. Marsupial pathway in humans / Anna Biason-Lauber, Amit V. Pandey, Walter L. Miller, Christa E. Fluck --
5. Androgen insensitivity syndrome / Charles Sultan, Pascal Philibert, Laura Gaspari, Francoise Audran, Laurent Maimoun, Nicolas Kalfa, Francoise Paris --
6A. Apparent mineralocorticoid excess / Mabel Yau, Saroj Nimkarn --
6B. The history, biology, and pathophysiology of apparent mineralocorticoid excess / John W. Funder --
6C. Glucocorticoid-remediable aldosteronism / Florencia Halperin, Robert G. Dluhy --
7. The genetics of ovotesticular disorders of sex development / Hayk Barseghyan, Eric Vilain --
8. The persistent Mullerian duct syndrome / Nathalie Josso, Richard L. Cate, Jean-Yves Picard --
9. Treatment and outcome of congenital adrenal hyperplasia : current reconstructive surgery / Richard C. Rink, Benjamin Whittam. 10. Psychoendocrinology of congential adrenal hyperplasia / Heino F.L. Meyer-Bahlburg --
11. Nuclear receptor co-regulators / David M. Lonard, Bert W. O'Malley --
12. Genetics of adrenal tumors / Antonio M. Lerario, Thomas J. Giordano, Gary D. Hammer --
13A. Animal models of adrenal genetic disorders / Felix Beuschlein --
13B. The impact of genetic steroid disorders on human fertility / David E. Reichman, Zev Rosenwaks --
13C. Preimplantation diagnosis and other modern methods for prenatal diagnosis / Joe Leigh Simpson --
13D. Geographical endocrinology of genetic steroid disorders / Nicole Reisch, Ursula Kuhnle --
13E. Debates and controversies in genetic steroid disorders / Phyllis W. Speiser --
13F. Genetic factors in Cushing disease pathogenesis / Alan A. Parsa, Shlomo Melmed --
13G. Case reports of unsolved mysteries of steroid disorders : 46,XY DSD with one clue / Amrit Bhangoo, Svetlana Ten.
Responsibility: edited by Maria I. New, MD, Professor of Pediatrics, Professor of Genetics and Genomic Sciences, Director, Adrenal Steroid Disorders, Mount Sinai School of Medicine, New York, NY, USA, Oksana Lekarev, DO, Assistant Professor of Pediatrics, Weill Cornell Medical College, New York, NY, USA, Assistant Attending Pediatrician, New York-Presbyterian Hospital, New York, NY, USA, Alan Parsa, MD, Associate Faculty Member, Division of Endocrinology Diabetes and Metabolism, Cedars-Sinai Medical Center, Los Angeles, CA, USA, Tony T. Yuen, PhD, Instructor Medicine, Endocrinology, Diabetes and Bone Disease, Mount Sinai School of Medicine, New York, NY, USA, Bert O'Malley, MD, Professor and Chair, Department of Molecular and Cellular Biology, Baylor College of Medicine, One Baylor Plaza, Houston, TX, USA, Gary D. Hammer, MD, PhD, Millie Schembechler Professor of Adrenal Cancer, Director, Endocrine Oncology Program, Comprehensive Cancer Center, Director, Center for Organogenesis, Department of Internal Medicine, Metabolism, Endocrinology & Diabetes, Department of Molecular & Integrative Physiology, Department of Cell & Molecular Biology, University of Michigan, Ann Arbor, MI, USA.

Abstract:

Addressing steroid disorders from hormonal, genetic, psychological, and surgical perspectives, this title teaches the best strategies and most effective use of genetic information in the patient  Read more...

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"Appropriate for both novice and experienced researchers, this collection demonstrates that the genetic basis has been located for each steroid disorder causing clinical and bioclinical abnormalities Read more...

 
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