Genetic Steroid Disorders

Forfatter: info mangler
Bog
  • Format
  • Bog, hardback
  • Engelsk

Beskrivelse

This is a comprehensive book addressing steroid disorders from hormonal, genetic, psychological, and surgical perspectives. It is meant to educate adult and pediatric endocrinologists, clinical geneticists, genetic counselors, reproductive endocrinologists, neonatologists, urologists, and psychoendocrinologists. It will assist these specialists in the diagnosis and treatment of steroid disorders. The book is written for postgraduate and faculty-level physicians. The content consists of steroid disorders, genetic bases for the disorder and case presentations of each disorder.

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Detaljer
  • SprogEngelsk
  • Sidetal406
  • Udgivelsesdato31-10-2013
  • ISBN139780124160064
  • Forlag Academic Press Inc
  • FormatHardback
Størrelse og vægt
  • Vægt1370 g
  • coffee cup img
    10 cm
    book img
    21,6 cm
    27,6 cm

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    Cancer Sexuality Infertility Gender Mutation Epidemiology Estrogens Ethnicity Hypertension Insulin resistance. Reproduction Steroid hormones Transcription Quality of life Homeostasis Prenatal diagnosis Heme oxygenase Treatment Cholesterol Neuroanatomy Mitochondria Hydrocortisone Testosterone Ovary Puberty Growth Hormone Androstenedione Hypospadias Preimplantation Diagnosis Testis Sex determination Disorders of Sex Development cognitive development Adrenocortical Carcinoma Gender role Steroidogenesis Congenital Adrenal Hyperplasia 46 Height Nuclear receptors Aldosterone Androgen Androgen Receptor Primary amenorrhea Germ cell tumor 17 Androgen action Ambiguous Genitalia Star Steroid ACTH Pituitary tumor Adrenal insufficiency Genetic Disease Adrenocortical tumors Intersex SRÜ Mouse model Vaginoplasty Labioplasty TGF-ß Androgen insensitivity syndrome Corticotroph adenoma 11ß-hydroxylase deficiency 17ß-hydroxysteroid dehydrogenase type 3 (17ß-HSD3) deficiency 17ß-hydroxysteroid dehydrogenase 3 17-hydroxylase 21-hydroxylase deficiency 20-lyase 3ß-HSD deficiency 3ß-hydroxysteroid dehydrogenase Adrenal hyperplasia adrenal hypoplasia adrenal development adrenocortical tumorigenesis adrenocorticotropic hormone (ACTH) ambiguous genitalia/disorders of sexual development (DSD) aromatase deficiency (AD) aromatase excess syndrome (AES) anti-Müllerian hormone receptor aromatase inhibitors (AIs) adrenal agenesis adrenal growth adrenal tumorigenesis apparent mineralocorticoid excess aromatase gene (CYP19A1) polymorphisms aromatase knockout (ArKO) mice biochemical abnormalities bone maturation and maintenance Anti-müllerian hormone Antley-Bixler syndrome (ABS) co-activators Chorionic villus sampling co-regulators CYP11A1 CYP3A4 Dihydrotestosterone clitoroplasty disorders of sexual differentiation (DSD) CYP17A1 brain functioning CYP21A2 enzyme deficiency clitoromegaly fetal androgens clinical abnormalities congenital adrenal hyperplasia (CAH) Gonad corticotroph cell co-repressors Hermaphrodite gender identity/gender role behavior hypokalemia disorders of sexual development Leydig cell hypoplasia endocrine tumor syndromes fetal sex determination mineralocorticoid receptor molecular markers of prognosis LHCGR mineralocorticoid P450 oxidoreductase deficiency (PORD) glucocorticoid remediable aldosteronism Niemann-Pick type C disease (NPC) human chorionic gonadotropin (HCG) genome-wide expression profiles ovotesticular disorders of sex development P450 oxidoreductase (POR) HSD17B3 gene pro-opiomelanocortin (POMC) sex development psychiatric outcome Sf1 (NR5A1) testosterone synthesis defect tall stature steroid 11ß-hydroxysteroid dehydrogenase type 2 surgical management of congenital adrenal hyperplasia XY DSD luteinizing hormone releasing hormone analog Wolman disease XY disorder of sex development (DSD) Müllerian-inhibiting substance prenatal dexamethasone treatment pseudohermaphrodite P450scc steroid disorders transgenic animal model transgenic zebrafish model Psychosocial Care virilization StAR deficiency Steroid synthesis sexual infantilism Short stature

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