標(biāo)題: Titlebook: Disorders of Steroidogenesis; Guide to Steroid Pro Gill Rumsby,Gary M. Woodward Book 2019 Springer International Publishing AG, part of Spr [打印本頁] 作者: hearken 時(shí)間: 2025-3-21 18:41
書目名稱Disorders of Steroidogenesis影響因子(影響力)
書目名稱Disorders of Steroidogenesis影響因子(影響力)學(xué)科排名
書目名稱Disorders of Steroidogenesis網(wǎng)絡(luò)公開度
書目名稱Disorders of Steroidogenesis網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Disorders of Steroidogenesis被引頻次
書目名稱Disorders of Steroidogenesis被引頻次學(xué)科排名
書目名稱Disorders of Steroidogenesis年度引用
書目名稱Disorders of Steroidogenesis年度引用學(xué)科排名
書目名稱Disorders of Steroidogenesis讀者反饋
書目名稱Disorders of Steroidogenesis讀者反饋學(xué)科排名
作者: nonplus 時(shí)間: 2025-3-21 23:42
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作者: oracle 時(shí)間: 2025-3-22 02:40 作者: AORTA 時(shí)間: 2025-3-22 06:31
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.作者: calumniate 時(shí)間: 2025-3-22 08:58
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 作者: 是比賽 時(shí)間: 2025-3-22 15:36
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作者: 是比賽 時(shí)間: 2025-3-22 18:11
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 作者: 咒語 時(shí)間: 2025-3-23 00:56 作者: semiskilled 時(shí)間: 2025-3-23 03:52 作者: vascular 時(shí)間: 2025-3-23 07:20 作者: Acclaim 時(shí)間: 2025-3-23 10:50
Synthesis Lectures on Software Engineeringtion of steroids, whether glucocorticoids, mineralocorticoids or androgens and their precursors. With increasing dedifferentiation, the abnormal steroid output by tumours may not be detected by routine serum hormone assays, and therefore urine steroid profile can be invaluable for the identification作者: CAB 時(shí)間: 2025-3-23 14:02 作者: 不持續(xù)就爆 時(shí)間: 2025-3-23 19:19 作者: persistence 時(shí)間: 2025-3-23 23:45 作者: 高度 時(shí)間: 2025-3-24 06:04
Test Your Skills in C# ProgrammingThis introductory chapter presents a simple account of steroid structure, chemistry and nomenclature along with a description of relevant aspects of steroidogenesis and steroid metabolism. This introductory chapter provides a background for the disease specific chapters that follow.作者: Accolade 時(shí)間: 2025-3-24 10:15
Test Your Skills in C# ProgrammingA brief review of adrenal physiology and steroidogenesis is given followed by a more comprehensive overview of adrenal pathophysiology. Inherited and acquired steroidogenic pathologies are described in the context of steroid excess and steroid deficiency.作者: 消音器 時(shí)間: 2025-3-24 14:13
TestGoal and the Ten Test PrinciplesThe 11β-hydroxylase enzyme catalyses the final step in cortisol biosynthesis. Deficiency of the enzyme accounts for approximately 5% of cases of congenital adrenal hyperplasia and is characterised by virilisation, hypertension and an excessive output of urinary metabolites derived from the cortisol precursor, 11-deoxycortisol.作者: 意外 時(shí)間: 2025-3-24 16:53 作者: Lumbar-Stenosis 時(shí)間: 2025-3-24 22:18
Linda Makovická Osvaldová,Widya FatriasariCushing’s syndrome is the name given to a group of symptoms resulting from glucocorticoid excess. The majority of cases are the result of steroid administration, but pituitary, adrenal and ectopic causes also occur. The urine steroid profile is primarily useful for the investigation of adrenal Cushing’s syndrome.作者: 殘忍 時(shí)間: 2025-3-25 02:16 作者: GRAVE 時(shí)間: 2025-3-25 05:40
Overview of Adrenocortical Pathophysiology,A brief review of adrenal physiology and steroidogenesis is given followed by a more comprehensive overview of adrenal pathophysiology. Inherited and acquired steroidogenic pathologies are described in the context of steroid excess and steroid deficiency.作者: 倔強(qiáng)一點(diǎn) 時(shí)間: 2025-3-25 10:27
,11β-Hydroxylase Deficiency,The 11β-hydroxylase enzyme catalyses the final step in cortisol biosynthesis. Deficiency of the enzyme accounts for approximately 5% of cases of congenital adrenal hyperplasia and is characterised by virilisation, hypertension and an excessive output of urinary metabolites derived from the cortisol precursor, 11-deoxycortisol.作者: 很像弓] 時(shí)間: 2025-3-25 15:15
Steroid Sulphotransferase and Sulphatase Deficiency,The conjugation of steroid hormones with sulphate provides a means of excretion and inactivation of such steroids but also, and perhaps more importantly, provides a pool of steroid that can be reactivated intracellularly. The relationship of the sulphotransferase and sulphatase enzymes is discussed along with problems arising in deficiency states.作者: wreathe 時(shí)間: 2025-3-25 16:04 作者: miniature 時(shí)間: 2025-3-25 23:10 作者: 情感脆弱 時(shí)間: 2025-3-26 02:02
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.作者: 最有利 時(shí)間: 2025-3-26 07:19
https://doi.org/10.1007/978-3-642-14740-1iew of cholesterol biosynthesis is presented with more in-depth coverage of two disorders in which a urine steroid profile can play a role in the diagnosis: cytochrome P450 oxidoreductase deficiency and Smith-Lemli-Opitz syndrome.作者: 颶風(fēng) 時(shí)間: 2025-3-26 11:07 作者: 暫時(shí)過來 時(shí)間: 2025-3-26 15:37
Gill Rumsby,Gary M. WoodwardOnly text for steroid profile interpretation.Contains graphic representations and illustrations.Utilises unique reference data collected over 30 years of clinical practice作者: 討厭 時(shí)間: 2025-3-26 16:56
http://image.papertrans.cn/e/image/281485.jpg作者: 圖表證明 時(shí)間: 2025-3-26 22:04 作者: separate 時(shí)間: 2025-3-27 03:57 作者: 一條卷發(fā) 時(shí)間: 2025-3-27 05:44 作者: 壓倒性勝利 時(shí)間: 2025-3-27 10:48
Adrenal Insufficiency, gland, rare inherited disorders or secondary to hypothalamic and pituitary disturbance..Urine steroid profiles are primarily of use in the evaluation of suspected biosynthetic defects but may also be required for the initial investigation of an early presentation of adrenal failure of any cause.作者: Forehead-Lift 時(shí)間: 2025-3-27 16:35 作者: 防銹 時(shí)間: 2025-3-27 17:46 作者: 分解 時(shí)間: 2025-3-28 00:57
,3β-Hydroxysteroid Dehydrogenase/Isomerase Deficiency,yperplasia and of 46XY and 46XX disorders of sex development (DSD). The disorder is characterised by excretion of excessive amounts of steroids with a double bond in the steroid B ring, the so-called Δ5 steroids, including dehydroepiandrosterone (DHEA) and its metabolites.作者: Painstaking 時(shí)間: 2025-3-28 03:23 作者: 做事過頭 時(shí)間: 2025-3-28 07:24
Aldosterone Synthase Deficiency,nherited as an autosomal recessive trait due to loss of function mutations in ., and it is extremely rare. The characteristic biochemical features are hyperreninaemic hypoaldosteronism. It is possible to make the diagnosis of this disorder using a urine steroid profile taken during a salt-losing episode.作者: Microaneurysm 時(shí)間: 2025-3-28 13:57
,17β-Hydroxysteroid Dehydrogenase Deficiency,lar androgen production - a similar phenotype to androgen insensitivity and 5α-reductase deficiency. Biochemical diagnosis can be made by measurement of serum steroids prior to gonadectomy; otherwise genetic testing is essential.作者: Adenoma 時(shí)間: 2025-3-28 17:06 作者: Delirium 時(shí)間: 2025-3-28 21:06 作者: 轉(zhuǎn)向 時(shí)間: 2025-3-28 23:46
Steroid-Producing Tumours,id output by tumours may not be detected by routine serum hormone assays, and therefore urine steroid profile can be invaluable for the identification of these intermediates. In addition, the pattern of metabolites produced is proving to be an aid to the classification of neoplasms.作者: intrude 時(shí)間: 2025-3-29 06:10 作者: Instrumental 時(shí)間: 2025-3-29 09:40
r 30 years of clinical practice.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 thes作者: 準(zhǔn)則 時(shí)間: 2025-3-29 11:29 作者: savage 時(shí)間: 2025-3-29 19:08
Testen von Informationssystemenicoids and adrenal androgens. Low levels of their respective metabolites are therefore observed in the urine steroid profiles of patients with either condition. Steroid synthesis in the gonads is also impaired. While no characteristic markers of disease are present, a urine steroid profile is useful in order?to exclude other forms of CAH.作者: Acquired 時(shí)間: 2025-3-29 22:28
Neutrinos Within the Standard Modelnherited as an autosomal recessive trait due to loss of function mutations in ., and it is extremely rare. The characteristic biochemical features are hyperreninaemic hypoaldosteronism. It is possible to make the diagnosis of this disorder using a urine steroid profile taken during a salt-losing episode.作者: Alveoli 時(shí)間: 2025-3-30 00:47 作者: 女上癮 時(shí)間: 2025-3-30 05:32 作者: ATRIA 時(shí)間: 2025-3-30 11:52
Testing Modern Biostratigraphical Methodsboth enzymes have been described and are characterised biochemically by an abnormal ratio of cortisol to cortisone metabolites in a urine steroid profile. The conditions have markedly different phenotypes: 11β-HSD2 is similar to Cushing’s syndrome and 11β-HSD1 characterised by androgen excess.作者: 序曲 時(shí)間: 2025-3-30 15:04 作者: 冒失 時(shí)間: 2025-3-30 18:35 作者: 就職 時(shí)間: 2025-3-30 20:48
Book 2019r 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 pr作者: Cacophonous 時(shí)間: 2025-3-31 01:06
Steroid Profiling: Analytical Perspectives, tandem–mass spectrometry (LC–MS/MS) is the gold standard technique for the quantification of steroids, gas chromatography/mass spectrometry (GC/MS) remains the favoured technique for the investigation and diagnosis of disorders of steroidogenesis. The following chapter aims to provide the reader wi作者: 閑逛 時(shí)間: 2025-3-31 06:48 作者: Cocker 時(shí)間: 2025-3-31 10:56
,3β-Hydroxysteroid Dehydrogenase/Isomerase Deficiency,dal steroids. Enzyme deficiency therefore has profound effects on adrenal and gonadal function and is a rare cause of salt-losing congenital adrenal hyperplasia and of 46XY and 46XX disorders of sex development (DSD). The disorder is characterised by excretion of excessive amounts of steroids with a
