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内分泌系统疾病(第2版)(影印)/奈特图解医学全集第2卷

内分泌系统疾病(第2版)(影印)/奈特图解医学全集第2卷

作者:WILLIAMYOUNG
出版社:北京大学医学出版社出版时间:2018-02-01
开本: 其他 页数: 243
本类榜单:医学销量榜
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内分泌系统疾病(第2版)(影印)/奈特图解医学全集第2卷 版权信息

  • ISBN:9787565919435
  • 条形码:9787565919435 ; 978-7-5659-1943-5
  • 装帧:平装-胶订
  • 册数:暂无
  • 重量:暂无
  • 所属分类:>>

内分泌系统疾病(第2版)(影印)/奈特图解医学全集第2卷 本书特色

  The second edition of the Endocrine System volume of the Netter Collection is designed to provide physicians at all stages of training and practice with a visual guide to the anatomy, physiology, and pathophysiology of the endocrine glands. The first edition was published in 1965. In the intervening 5 decades, there have been remarkable developments in our understanding of endocrine disorders. The text has been entirely rewritten, but most of the anatomic and clinical artwork of Frank H. Netter, MD, has stood the test of time. Since new endocrine disorders and treatment approaches have been recognized over the past 50 years, new artwork has been added in every section, including the following: current surgical approaches to remove pituitary tumors, tests used in the diagnosis of Cushing syndrome, adrenal venous sampling for primary aldosteronism, Cushing syndrome caused by primary pigmented nodular adrenocortical disease, treatment of type 1 and type 2 diabetes mellitus, multiple endocrine neoplasia types 1 and 2, and von Hippel-Lindau syndrome. Carlos Machado, MD, James A. Perkins, MS, MFA, Kristen Wienandt Marzejon, MS, MFA, and John Craig, MD, have contributed outstanding new plates to this edition, as well as adapted and updated existing artwork. The accompanying text serves to illuminate and expand on the concepts demonstrated in the images.  The second edition of the Endocrine System volume of the Netter Collection is designed to provide physicians at all stages of training and practice with a visual guide to the anatomy, physiology, and pathophysiology of the endocrine glands. The first edition was published in 1965. In the intervening 5 decades, there have been remarkable developments in our understanding of endocrine disorders. The text has been entirely rewritten, but most of the anatomic and clinical artwork of Frank H. Netter, MD, has stood the test of time. Since new endocrine disorders and treatment approaches have been recognized over the past 50 years, new artwork has been added in every section, including the following: current surgical approaches to remove pituitary tumors, tests used in the diagnosis of Cushing syndrome, adrenal venous sampling for primary aldosteronism, Cushing syndrome caused by primary pigmented nodular adrenocortical disease, treatment of type 1 and type 2 diabetes mellitus, multiple endocrine neoplasia types 1 and 2, and von Hippel-Lindau syndrome. Carlos Machado, MD, James A. Perkins, MS, MFA, Kristen Wienandt Marzejon, MS, MFA, and John Craig, MD, have contributed outstanding new plates to this edition, as well as adapted and updated existing artwork. The accompanying text serves to illuminate and expand on the concepts demonstrated in the images.
  The book is organized in 8 sections, which correspond to the glands and components of the endocrine system: pitLutary and hypoLhalamus, thyroid, adrenal, reproduction, pancreas, bone and calcium, lipids and nutrition, and genetics and endocrine neoplasia. In some cases, the Netter drawings are supplemented with modern diagnostic images (e.g., computed tomography and magnetic resonance imaging). The original Netter edition and the new illustrations focus on embryology, gross anatomy, histology, physiology, pathology, clinical manifestations of disease, diagnostic modalities, and surgical and therapeutic techniques.
  Writing an "update" that spans 5 decades has been a daunting challenge. However, this new edition will serve to preserve and provide context for the original Netter illustrations well into the twenty-first century. This work is not a complete textbook of endocrinology, but rather it is a visual tour of the highlights of this medical discipline. I hope readers find the artwork and accompanying text useful guides as they navigate the world of endocrinology.
  I gratefully acknowledge my colleagues and patients at Mayo Clinic who have provided me with the clinical experience, perspective, and insights to address the broad field of endocrinology. The editorial and production staffs at Elsevier have been very supportive at every step from initial general concepts to final publication. I am indebted to the incredible second generation of Netter artists. I also want to thank my daughter, Abbie L. Abboud, MS, CGC, ELS, for her invaluable help in medical editing and providing guidance on clarity of thought and concept. Finally, I dedicate this book to my family-their encouragement and support have been inspirational during the 2 years it took to produce the second edition of the EndoLYine System volume of the Netter Collection.

内分泌系统疾病(第2版)(影印)/奈特图解医学全集第2卷 内容简介

奈特图解医学全集是世界有名的奈特品牌的主打书,整套书分为9大系统疾病,运用传统的图解形式,从基础到临床,进行了详细的精解。全书绘图精美,语言简洁地道,可读性强,无论是对临床医学生还是年轻医生,都是系统学习,掌握知识的重要参考书。

内分泌系统疾病(第2版)(影印)/奈特图解医学全集第2卷 目录

SECTION 1 PITUITARY AND HYPOTHALAMUS 1-1 Development of the Pituitary Cland 1-2 Divisions of the Pituitary Cland and Relationship to the Hypothalamus 1-3 Blood Supply of the Pituitary Cland 1-4 Anatomy and Relationships of the Pituitary Gland 1-5 Relationship of the Pituitary Cland to the Cavernous Sinus 1-6 Relationships of the Sella Turcica 1-7 Anterior Pituitary Hormones and Feedback Control 1-8 Posterior Pituitary Gland 1-9 Manifestations of Suprasellar Disease 1-10 Craniopharyngioma 1-11 Effects of Pituitary Tumors on the Visual Apparatus 1-12 Nontumorous Lesions of the Pituitary Gland and Pituitary Stalk 1-13 Pituitary Anterior Lobe Deficiency in Childhood and Adolescence in Boys 1-14 Pituitary Anterior Lobe Deficiency in Adults 1-15 Selective and Partial Hypopituitarism 1-16 Severe Anterior Pituitary Deficiency or Panhypopituitarism 1-17 Postpartum Pituitary Infarction (Sheehan Syndrome) 1-18 Pituitary Apoplexy 1-19 Pituitary Cigantism 1-20 Acromegaly 1-21 Prolactin-Secreting Pituitary Tumor 1-22 Corticotropin-Secreting Pituitary Tumor 1-23 Nelson Syndrome 1-24 Clinically Nonfunctioning Pituitary Tumor 1-25 Secretion and Action of Oxytocin 1-26 Secretion and Action of Vasopressin 1-27 Central Diabetes Insipidus 1-28 Langerhans Cell Histiocytosis in Children 1-29 Langerhans Cell Histiocytosis in Adults 1-30 Tumors Metastatic to the Pituitary 1-31 Surgical Approaches to the PituitarySECTION 2 THYROID 2-1 Anatomy of the Thyroid and Parathyroid Glands 2-2 Anatomy of the Thyroid and Parathyroid Glands(cont'd) 2-3 Development of the Thyroid and Parathyroid Clands 2-4 Development of the Thyroid and Parathyroid Glands(cont'd) 2-5 Congenital Anomalies of the Thyroid Gland 2-6 Effects of Thyrotropin on the Thyroid Gland 2-7 Physiology of Thyroid Hormones 2-8 Graves Disease 2-9 Graves Disease(cont'd) 2-10 Graves Ophthalmopathy 2-11 Thyroid Pathology in Craves Disease 2-12 Clinical Manifestations of Toxic Adenoma and Toxic Multinodular Goiter 2-13 Pathophysiology of Toxic Adenoma and Toxic Multinodular Coiter 2-14 Clinical Manifestations of Hypothyroidism in Adults 2-15 Clinical Manifestations of Hypothyroidism in Adults (cont'd) 2-16 Clinical Manifestations of Hypothyroidism in Adults(cont'd) 2-17 Congenital Hypothyroidism 2-18 Euthyroid Goiter 2-19 Gross Pathology of Coiter 2-20 Etiology of Nontoxic Goiter 2-21 Chronic Lymphocytic Thyroiditis and Fibrous Thyroiditis 2-22 Subacute Thyroiditis 2-23 Papillary Thyroid Carcinoma 2-24 Follicular Thyroid Carcinoma 2-25 Medullary Thyroid Carcinoma 2-26 Hurthle Cell Thyroid Carcinoma 2-27 Anaplastic Thyroid Carcinoma 2-28 Tumors Metastatic to the ThyroidSECTION 3 ADRENAL 3-1 Development of the Adrenal Clands 3-2 Anatomy and Blood Supply of the Adrenal Glands 3-3Anatomy and Blood Supply of the Adrenal Clands(cont'd) 3-4 Innervation of the Adrenal Clands 3-5 Histology of the Adrenal Clands 3-6 Biosynthesis and Metabolism of Adrenal Cortical Hormones 3-7 Biosynthesis and Metabolism of Adrenal Cortical Hormones(cont'd) 3-8 The Biologic Actions of Cortisol 3-9 Cushing Syndrome-Clinical Findings 3-10 Tests Used in the Diagnosis of Cushing Syndrome 3-11 Cushing Syndrome:Pathophysiology Cushing Syndrome Caused by Primary 3-12 Pigmented Nodular Adrenocortical Disease Major Blocks in Abnormal 3-13 Steroidogenesis 3-14 Classic Congenital Adrenal Hyperplasia 3-15 The Biologic Actions of Adrenal Androgens 3-16 Adult Androgenital Syndromes 3-17 The Biologic Actions of Aldosterone 3-18 Primary Aldosteronism 3-19 Adrenal Venous Sampling for Primary Aldosteronism 3-20 Renin-Angiotensin-Aldosterone System and Renovascular Hypertension 3-21 Acute Adrenal Failure-Adrenal Crisis 3-22 Chronic Primary Adrenal Failure- Addison Disease 3-23 Laboratory Findings and Treatment of Primary Adrenal Insufficiency 3-24 Laboratory Findings and Treatment of Secondary Adrenal Insufficiency 3-25Adrenal Medulla and Catecholamines 3-26 Catecholamine SynthesisStorage SecretionMetabolismand Inactivation 3-27 Pheochromocytoma and Paraganglioma 3-28 Pheochromocytoma and Paraganglioma(cont'd) 3-29 Tumors Metastatic to the Adrenal ClandsSECTION 4 REPRODUCTION 4-1 Differentiation of Conads 4-2 Differentiation of Genital Ducts 4-3Differentiation of External Cenitalia 4-4Testosterone and Estrogen Synthesis 4-5 Normal Puberty 4-6 Normal Puberty(cont'd) 4-7 Normal Puberty (cont'd) 4-8 Normal Puberty(cont'd) 4-9 Precocious Puberty 4-10 Precocious Puberty(cont'd) 4-11 Precocious Puberty(cont'd) 4-12 Disorders of Sex Development 4-13Disorders of Sex Development (cont'd) 4-14 Disorders of Sex Development (cont'd) 4-15 Disorders of Sex Development (cont'd) 4-16 Errors in Chromosomal Sex 4-17 Klinefelter Syndrome 4-18 Turner Syndrome(Gonadal Dysgenesis) 4-19 Turner Syndrome(Conadal Dysgenesis) (cont'd) 4-20 Turner Syndrome(Conadal Dysgenesis) (cont'd) 4-21 Hirsutism and Virilization 4-22 Hirsutism and Virilization (cont'd) 4-23 Influence of Gonadal Hormones on the Female Reproductive Cycle from Birth to Old Age 4-24 Functional and Pathologic Causes of Uterine Bleeding 4-25 Gynecomastia 4-26 GalactorrheaSECTION 5 PANCREAS 5-1 Pancreas Anatomy and Histology 5-2 Exocrine Functions of the Pancreas 5-3Normal Histology of Pancreatic Islets 5-4 Insulin Secretion 5-5 Actions of Insulin 5-6 Clycolysis 5-7 Tricarboxylic Acid Cycle 5-8 Clycogen Metabolism 5-9 Consequences of Insulin Deprivation 5-10 Diabetic Ketoacidosis 5-11 Type l Diabetes Mellitus 5-12 Type 2 Diabetes Mellitus 5-13Diabetic Retinopathy 5-14 Complications of Proliferative Diabetic Retinopathy 5-15 Diabetic Nephropathy 5-16 Diabetic Neuropathy 5-17 Atherosclerosis in Diabetes 5-18 Vascular Insufficiency in Diabetes:The Diabetic Foot 5-19 Diabetes Mellitus in Pregnancy 5-20 Treatment of Type 2 Diabetes Mellitus 5-21 Treatment of Type 1 Diabetes Mellitus 5-22 Insulinoma 5-23 Primary Pancreatic β-Cell HyperplasiaSECTION 6 BONE AND CALCIUM 6-1 Histology of the Normal Parathyroid Clands 6-2 Physiology of the Parathyroid Clands 6-3 Bone Remodeling Unit 6-4 Pathophysiology of Primary Hyperparathyroidism 6-5 Pathology and Clinical Manifestations of Primary Hyperparathyroidism 6-6 Tests for the Differential Diagnosis of the Causes of Hypercalcemia 6-7 Renal Osteodystrophy 6-8 Renal Osteodystrophy:Bony Manifestations 6-9 Histology of the Parathyroid Clands in Hyperparathyroidism 6-10 Pathophysiology of Hypoparathyroidism 6-11 Clinical Manifestations of Acute Hypocalcemia 6-12 Pathophysiology of Pseudohypoparathyroidism 6-13 Clinical Manifestations of Pseudohypoparathyroidism Type la 6-14 Pathogenesis of Osteoporosis 6-15 Osteoporosis in Postmenopausal Women 6-16 Osteoporosis in Men 6-17 Clinical Manifestations of Osteoporotic Vertebral Compression Fractures 6-18 Nutritional-Deficiency Rickets and Osteomalacia 6- Pseudovitamin D-Deficiency Rickets and Osteomalacia 6-20 Hypophosphatemic Rickets 6-21 Clinical Manifestations of Rickets in Childhood 6-22 Clinical Manifestations of Osteomalacia in Adults 6-23 Paget Disease of the Bone 6-24 Pathogenesis and Treatment of Paget Disease of the Bone 6-25 Osteogenesis Imperfecta 6-26 Osteogenesis Imperfecta(cont'd) 6-27 HypophosphatasiaSECTION 7 LIPIDS AND NUTRITION 7-1 Cholesterol Synthesis and Metabolism 7-2 Gastrointestinal Absorption of Cholesterol and Triglycerides 7-3 Regulation of Low-Density Lipoprotein Receptor and Cholesterol Content 7-4 High-Density Lipoprotein Metabolism and Reverse Cholesterol Transport 7-5 Hypercholesterolemia 7-6 Hypercholesterolemic Xanthomatosis 7-7 Hypercholesterolemic Xanthomatosis (cont'd) 7-8 Abetalipoproteinemia and Tangier Disease 7-9 Hypertriglyceridemia 7-10 Clinical Manifestations of Hypertriglyceridemia 7-11 Clinical Manifestations of Hypertriglyceridemia (cont'd) 7-12 Atherosclerosis 7-13 Atherosclerosis(cont'd) 7-14 Atherosclerosis Risk Factors 7-15 Metabolic Syndrome 7-16 Mechanisgg of Action of Lipid-Lowering Agents 7-17 Treatment of Hyperlipidemia 7-18 Absorption of Essential Vitamins 7-19 Vitamin B:Deficiency:Beriberi 7-20 Vitamin B3 Deficiency:Pellagra 7-21 Vitamin C Deficiency:Scurvy 7-22 Vitamin A Deficiency 7-23Celiac Disease and Malabsorption 7-24 Lysosomal Storage Disorders: Sphingolipidoses 7-25 Anorexia Nervosa 7-26 Obesity 7-27 Surgical Treatment Options for ObesitySECTION 8 GENETICS AND ENDOCRINE NEOPLASIA 8-1 Multiple Endocrine Neoplasia Type 1 8-2 Multiple Endocrine Neoplasia Type 2 8-3Multiple Endocrine Neoplasia Type 2(cont'd) 8-4Von Hippel-Lindau Syndrome 8-5 Neurofibromatosis Type 1(von Recklinghausen Disease) 8-6Clinical Manifestations of Autoimmune Polyglandular Syndrome Type 1 8-7 Carcinoid SyndromeGLOSSARY OF ABBREVIATIONSREFERENCESINDEX
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