青春期疾病

青春期疾病

青春期疾病》是2008年科學出版社出版的圖書,作者是馬爾蒂尼

基本介紹

  • 書名:青春期疾病
  • 作者:(英國)馬爾蒂尼
  • ISBN:9787030209375
  • 頁數:459頁
  • 出版社:科學出版社
  • 出版時間:2008年4月1日
  • 開本:16
  • 正文語種: 簡體中文
  • 條形碼: 9787030209375
  • 尺寸: 26.2 x 19 x 2.8 cm
  • 尺寸:重量: 998 g
內容簡介,圖書目錄,

內容簡介

青春期疾病》百科全書意在成為跨越內分泌系統的多個不同方面的有用和綜合的信息來源。
青春期疾病》中,來自全世界的約800名內分泌領域著名的臨床醫師和科學家對近500個題目進行了探討。有興趣的讀者可以在書中找到關於新發現激素的文章,如胃促生長素和瘦素;也可以找到關於一些疾病的文章,如高血壓、低血糖症、糖尿病、癌症、骨質疏鬆、腎結石、Graves病、Paget骨病、阿爾茨海默病、Noonan綜合徵、朗格漢斯細胞疾病、庫欣綜合徵、甲狀腺和垂體功能失調;以及一些探討如下專題的文章:內分泌系統的進化、激素的作用機制、衰老的內分泌衰竭和神經系統與內分泌系統的整合作用。

圖書目錄

Adrenarche,Premature(腎上腺功能早現)
Agonadism,Male and Female(男性和女性無性腺症)
Androgens,Gender and Brain Differentiation(雄激素,性別和腦分化)
Anorexia Nervosa(神經性厭食)
Auxology,Childhood(JL童發育學)
Bardet Biedl Syndrome(Bardet-Biedl綜合徵)
Beckwith-Wiedemann Syndrome(BWS,Beckwith Wiedemann綜合徵)
Body Composition During Growth(生長中的機體組成)
Body Proportions(身體比例)
Childhood Cancer,Endocrine Effects of(兒童癌症的內分泌效應)
Congenital Adrenal Hyperplasia,Prenatal Diagnosis and Therapy(先天性腎上腺增生症的產前診斷與治療)
Congenital Lipoid Adrenal Hyperplasia(先天性類脂質性腎上腺增生症)
Constitutional Delay of Growth and Puberty(CDGP,生長及青春期體質性延遲)
Craniopharyngiomas(顱咽管瘤)
Delayed Puberty and Hypogonadism,Female(女性青春期延遲及性腺功能減退)
Delayed Puberty and Hypogonadism,Male(男性青春期延遲及性腺功能減退)
Delayed Puberty,Male(男性青春期延遲)
Eating Disorders and the Reproductive Axis(進食障礙及生殖軸)
Feto—Placental Unit(胎兒一胎盤單位)
Gender Assignment and Psychosocial Management(性別分配與心理治療)
Genes and Gene Defects Affecting Gonadal Development and Sex Determination(影響性腺發育和性別決定的基因及基因缺陷)
Gigantism:Excess of Growth Hormone(巨人症:生長激素分泌過多)
Growth and Chronic Disease(生長與慢性疾病)
Growth and Glucocorticoids(生長與糖皮質激素)
Growth Hormone(GH,生長激素)
Growth Hormone-Binding Proteins(生長激素結合蛋白)
Growth Hormone Deficiency,Genetic(遺傳性生長激素不足)
Growth Hormone Insensitivity(生長激素不敏感)
Growth,Normal Patterns and Constitutional Delay(正常生長模式和體質性生長延遲)
Hamartoma,Pituitary(垂體錯構瘤)
11B-Hydroxylase Deficiency(11(}I羥化酶缺乏症)
21-Hydroxylase Deficiency,Classical(經典21一羥化酶缺乏症)
21一Hydroxylase Deficiency,Genetics of(21一羥化酶缺乏症的遺傳學)
17a—Hydroxylase/17,20—Lyase Deficiency(17曠羥化酶/17,20-裂解酶缺乏症)
3p—Hydroxysteroid Dehydrogenase Deficiency(3l}羥基類固醇脫氫酶缺乏症)
Hyperthyroidism,Childhood and Adolescence(JL童及青少年甲狀腺功能亢進症)
Hypothalamic Hypogonadism(下丘腦性性腺功能減退症)
Hypothyroidism,Congenital,Long—Term Follow-Up(先天性甲狀腺功能減退症的長期隨訪)
Hypothyroidism,Congenital,Screening Programs(先天性甲狀腺功能減退症的篩j流程)
Intrauterine Growth Retardation(宮內生長遲滯)
Kallmann’s Syndrome and Idiopathic Hypogonadotropic Hypogonadism(Kallmann綜合徵和特發性低促性腺激素性性腺功能減退症)
Klinefelter’s Syndrome(克氏綜合徵)
Langerhans Cell Disease(朗格漢斯細胞疾病)
McCune-Albright Syndrome(McCune-Albright綜合徵)
Melatonin(褪黑素)
Neurofibromatosis(多發性神經纖維瘤)
Newborn Ambiguous Genitalia Management(新生兒兩性畸形的處理)
Noonan Syndrome(努南綜合徵)
Obesity,Childhood and Adolescence(JL童期和青春期肥胖)
Pituitary Gland:Growth and Growth Failure(垂體:生長與生長障礙)
Postnatal Non-Endocrine Overgrowth(出生後非內分泌性過度生長)
Postnatal Normal Growth and Its Endocrine Regulation(出生後正常生長及其內分泌調節)
Prader-willi Syndrome(Prade卜willi綜合徵)
Precocious Puberty,Central(Female)(女性中樞性性早熟)
Precocious Puberty,Central(Male)(男性中樞性性早熟)
Precocious Puberty,Gonadotropin—Independent(非促性腺激素依賴型性早熟)
Pseudoprecocious Puberty,Female(女性假性性早熟)
Pseudoprecocious Puberty,Male(男性假性性早熟)
Puberty,Male:Mechanisms of Onset and Progression(男性青春期開始和發育的機制:Physical Activity and Growth(青春期:體育活動與發育)
Sexual Maturation,Female(女性性成熟)
Sexual Maturation,Male(男性性成熟)
Short Stature and Chromosomal Abnormalities(身材矮小症和染色體異常)
SHOX Disorders(5HOX基因缺陷)
Skeletal Development(骨骼發育)
Skeletal Development During Childhood and Adolescence(JL童期和青春期的骨骼發育)
Thalassemia,Endocrine Sequelae(地中海貧血與內分泌後遺症)
Turner Syndrome(特納綜合徵)
Undescended Testes(睪丸未降)
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