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Titlebook: Disorders of Steroidogenesis; Guide to Steroid Pro Gill Rumsby,Gary M. Woodward Book 2019 Springer International Publishing AG, part of Spr

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發(fā)表于 2025-3-21 18:41:37 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Disorders of Steroidogenesis
副標(biāo)題Guide to Steroid Pro
編輯Gill Rumsby,Gary M. Woodward
視頻videohttp://file.papertrans.cn/282/281485/281485.mp4
概述Only text for steroid profile interpretation.Contains graphic representations and illustrations.Utilises unique reference data collected over 30 years of clinical practice
圖書封面Titlebook: Disorders of Steroidogenesis; Guide to Steroid Pro Gill Rumsby,Gary M. Woodward Book 2019 Springer International Publishing AG, part of Spr
描述.This book covers the subject of steroid profiling for the diagnosis of disorders of steroidogenesis. Each chapter provides at least one case study for each of the listed disorders in order to illustrate the subtle and nuanced details required for the diagnosis of these conditions. General information is also given about the biology of these disorders and explanations of typical laboratory findings are provided..This book describes the steroid profile features and its interpretation, in addition to describing the pathophysiology, clinical indications for investigation, general endocrine investigations and genetic considerations for each of the congenital and acquired conditions..A valuable tool for day-to-day clinical and laboratory investigations of adrenal pathologies and disorders of steroidogenesis, as well as providing impetus to further study..
出版日期Book 2019
關(guān)鍵詞Steroidogenesis; Steroid Profiling; Biochemical Diagnosis; Congenital disorders; Adrenal pathologies
版次1
doihttps://doi.org/10.1007/978-3-319-96364-8
isbn_softcover978-3-030-07181-3
isbn_ebook978-3-319-96364-8
copyrightSpringer International Publishing AG, part of Springer Nature 2019
The information of publication is updating

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發(fā)表于 2025-3-21 23:42:46 | 只看該作者
Automatische Generierung von Testdaten,ital adrenal hyperplasia. The disorder is characterised by a variable degree of renal salt-losing caused by aldosterone insufficiency and virilisation as a result of exposure to excess androgens produced in utero and after birth in untreated patients. Urine steroid profiles allow early diagnosis and
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Ping Du,Maoke Chen,Akihiro Nakaoen synthesis in the male and is a cause of 46XY disorder of sex development. Overproduction of steroids with mineralocorticoid properties can lead to low renin hypertension in both sexes. The urine steroid profile is characterised by excess progesterone and corticosterone metabolites.
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Testen von Informationssystemenongenital adrenal hyperplasia (CAH) characterised by a complete or partial inability of the adrenal glands to synthesise glucocorticoids, mineralocorticoids and adrenal androgens. Low levels of their respective metabolites are therefore observed in the urine steroid profiles of patients with either
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Neutrinos Within the Standard Modelan present with a salt-losing crisis in infancy. Patients surviving this period may be asymptomatic in adulthood. Aldosterone synthase deficiency is inherited as an autosomal recessive trait due to loss of function mutations in ., and it is extremely rare. The characteristic biochemical features are
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Neutrinos Within the Standard Modelof the oxygen moiety at C17 of the steroid molecule. Deficiency of the type 3 enzyme leads to a disorder of sex development through failure of testicular androgen production - a similar phenotype to androgen insensitivity and 5α-reductase deficiency. Biochemical diagnosis can be made by measurement
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