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The Resource Pediatric Endocrinology : A Clinical Handbook

Pediatric Endocrinology : A Clinical Handbook

Label
Pediatric Endocrinology : A Clinical Handbook
Title
Pediatric Endocrinology
Title remainder
A Clinical Handbook
Creator
Subject
Language
eng
Cataloging source
MiAaPQ
Literary form
non fiction
Nature of contents
dictionaries
Pediatric Endocrinology : A Clinical Handbook
Label
Pediatric Endocrinology : A Clinical Handbook
Link
http://libproxy.rpi.edu/login?url=https://ebookcentral.proquest.com/lib/rpi/detail.action?docID=4514223
Publication
Copyright
Related Contributor
Related Location
Related Agents
Related Authorities
Related Subjects
Carrier category
online resource
Carrier category code
cr
Carrier MARC source
rdacarrier
Color
multicolored
Content category
text
Content type code
txt
Content type MARC source
rdacontent
Contents
  • Dedication -- Preface -- Acknowledgements -- Contents -- 1: Introduction to Pediatric Endocrinology: The Endocrine System -- Suggested Readings -- 2: The Evaluation of a Child or Adolescent with Possible Endocrine Disease -- The Medical History -- Physical Examination -- 3: Disorders of the Hypothalamic-Pituitary Axis -- Physiology -- Pathology -- Central Nervous System Tumors -- Craniopharyngioma -- Germinomas -- Pituitary Adenomas -- Other Central Nervous System Disorders -- Langerhans Cell Histiocytosis -- Postinfectious Inflammatory Lesions of the Central Nervous System, Vascular Abnormalities, and Head Trauma -- Irradiation of the Central Nervous System -- Developmental Defects of the Midline -- Septo-Optic and Optic Dysplasia -- The Solitary Median Maxillary Incisor Syndrome -- Idiopathic Hypopituitary Dwarfism -- Suggested Readings -- 4: The Posterior Pituitary Gland and Disorders of Vasopressin Metabolism -- Normal Vasopressin Physiology -- Diabetes Insipidus -- Central Diabetes Insipidus -- Nephrogenic Diabetes Insipidus -- Clinical Features of Diabetes Insipidus -- Diagnosis of Diabetes Insipidus -- Treatment of Central Diabetes Insipidus -- Treatment of Nephrogenic Diabetes Insipidus -- The Syndrome of Inappropriate Secretion of Antidiuretic Hormone -- Nephrogenic Syndrome of Inappropriate Antidiuresis -- Other Causes of Hyponatremia -- The Treatment of Syndrome of Inappropriate Secretion of Antidiuretic Hormone -- The Triphasic Response After Surgery for Craniopharyngioma -- Suggested Readings -- 5: Disorders of Growth -- Measurement of Growth -- Endocrine Factors in Postnatal Growth -- Growth Hormone -- Insulin-Like Growth Factor or IGF -- Epidermal Growth Factor -- Erythropoietin -- Oncogenes -- Dental Development -- Abnormalities of Growth -- Short Stature -- Nonendocrine Causes of Short Stature -- Constitutional Delay in Growth
  • Genetic Short Stature -- Idiopathic Short Stature -- Small for Gestational Age -- Turner Syndrome and SHOX Mutation -- Syndromes of Short Stature -- Noonan Syndrome -- Russell-Silver Dwarfism Syndrome -- Fetal Alcohol Syndrome -- Syndromes of Obesity and Short Stature -- Prader-Willi Syndrome -- Bardet-Biedl Syndrome -- Miscellaneous Syndromes -- Growth and Attention-Deficit Disorder -- Chronic Disease and Malnutrition -- Endocrine Causes of Short Stature -- Congenital Growth Hormone Deficiency -- Isolated GH Deficiency -- Combined Pituitary Defects -- GH Resistance -- Acquired GH Deficiency -- Central Nervous System Tumors -- Other Conditions -- Psychosocial Dwarfism -- Diagnosis of Growth Hormone Deficiency (Fig. 5.12) -- Growth Hormone Treatment of GH Deficiency and Other Disorders Approved for GH Treatment -- Other Endocrine Disorders -- Other Endocrine or Syndromic Conditions -- Hypothyroidism -- Cushing Syndrome -- Pseudohypoparathyroidism -- Rickets -- Diabetes Mellitus -- Diagnosis of Short Stature -- History and Physical Examination -- Tall Stature -- Nonendocrine Causes of Tall Stature -- Endocrine Etiologies of Tall Stature -- Diagnosis and Treatment of Tall Stature -- Suggested Readings -- 6: Disorders of the Thyroid Gland -- Normal Thyroid Physiology and Anatomy -- Fetal Thyroid Development in the Newborn -- Laboratory Evaluation -- Imaging of Thyroid -- Disorders of the Thyroid Gland -- Goiter -- Hypothyroidism -- Congenital Hypothyroidism (CH) -- Anatomical -- Biochemical -- Hypothalamic-Pituitary Abnormalities -- Thyroid-Binding Globulin Mutations -- Consumptive Hypothyroidism -- Exogenous Agents -- Transient Congenital Hypothyroidism and Variants -- Management of a Positive Neonatal Screen -- Acquired Hypothyroidism -- Autoimmune Thyroid Disease: Hashimotos Thyroiditis -- Other Causes for Acquired Hypothyroidism
  • Euthyroid Sick Syndrome -- Diagnosis of Hypothyroidism -- Treatment of Hypothyroidism -- Hyperthyroidism -- Neonatal Hyperthyroidism -- Older Children -- Diagnosis -- Treatment of Hyperthyroidism -- Medication -- Surgery -- Nuclear Medicine Therapy -- Thyroid Storm -- Thyroid Hormone Overdose -- Neoplasms -- Medullary Carcinoma of the Thyroid (MCT) -- Epithelial-Derived Differentiated Thyroid Cancer (DTC) -- Familial Nonmedullary Thyroid Carcinoma -- Papillary Carcinoma -- Follicular Thyroid Carcinoma -- Diagnosis -- Treatment of Thyroid Carcinoma -- Surgery -- Radiation -- Painful Thyroid Glands -- Hyperfunctioning Nodule -- Further Reading -- 7: Disorders of Calcium Metabolism and Bone -- Calcium Metabolism -- Storage and Absorption of Calcium -- The Calcium-Sensing Receptor -- Phosphate -- Magnesium -- Parathyroid Hormone and Parathyroid Hormone-Related Protein -- Vitamin D and Its Metabolites (Fig. 7.1) -- Calcitonin -- Alkaline Phosphatase -- Hypocalcemia (Fig. 7.2) -- Hypocalcemia in the Infant -- Early Neonatal Hypocalcemia -- Late Neonatal Hypocalcemia -- Diagnosis of Infantile Hypocalcemia -- Treatment of Newborns -- Hypocalcemia in the Child and Adolescent -- Hypoparathyroidism -- The Diagnosis of Hypoparathyroidism -- Treatment of Hypoparathyroidism -- Pseudohypoparathyroidism -- Magnesium Deficiency and Magnesium Excess -- Activating Mutations of the Calcium-{u00AD}Sensing Receptor -- Hyperphosphatemia -- Diagnosis of Hypocalcemia -- Normal Bone Growth -- Vitamin D and Calcium Deficiency -- Rickets (Table 7.2) -- Nutritional Rickets -- Hepatocellular Rickets -- Renal Osteodystrophy -- Anticonvulsant-Associated Rickets or Hypocalcemia -- Rickets of Prematurity -- Genetic Causes of Rickets -- Defects in Vitamin D Production or Action -- Hypophosphatemic Rickets -- Renal Tubular Acidosis -- Diagnosis of Rickets
  • Treatment of Vitamin D Deficiency (Table 7.3) -- Hypercalcemia -- Primary Hyperparathyroidism -- Familial Hypocalciuric Hypercalcemia -- Miscellaneous Causes -- Hypercalcemia of Malignancy -- Other Endocrine Disorders Causing Hypercalcemia -- Drug-Induced Hypercalcemia -- Milk Alkali Syndrome and Hypercalcemia of Renal Insufficiency -- Granulomatous Disease -- Immobilization Hypercalcemia -- Williams Syndrome -- Other Causes of Hypercalcemia -- Treatment of Hypercalcemia -- Evaluation of Hypercalcemia -- Osteoporosis -- Osteopenia of the Premature Infant -- Osteogenesis Imperfecta -- Increased Bone Mass Osteopetrosis -- Nonaccidental Bone Injuries -- Aluminum Toxicity -- Suggested Readings -- 8: Disorders of Sexual Differentiation -- Normal Sexual Differentiation -- Genotype -- Gonadal Sex -- Phenotypic Sex -- Social Gender -- Disorders of Sexual Differentiation -- 46, XX DSD: Conditions Causing Genetic Females to Become Virilized (Previously Called Female Pseudohermaphroditism) -- Virilizing Congenital Adrenal Hyperplasia -- 21-Hydroxylase Deficiency (*201910 ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY) -- Diagnoses -- Treatment -- Nonclassical CAH Treatment -- Fertility in CAH -- 11-Hydroxylase Deficiency -- 3-Hydroxysteroid Dehydrogenase Deficiency -- Maternal Sex Steroid Ingestion or Androgen-Producing Conditions -- Other Causes of 46, XX DSD -- P450-Oxidoreductase Deficiency -- Aromatase Deficiency and Estrogen Receptor Deficiency -- Mayer-Rokitansky-Küster-Hauser Syndrome -- 46, XX Gonadal Dysgenesis -- 46, XY DSD: Disorders Causing Inadequate Virilization of a Genetic Male (Previously Called Male Pseudohermaphroditism) -- 46, XY DSD with Enzymatic Deficiencies Involving the Gonads and the Adrenal Glands -- Smith-Lemli-Opitz Syndrome -- StAR Deficiency -- 3-Hydroxysteroid Dehydrogenase Deficiency
  • 17Ü-Hydroxylase Deficiency -- 46, XY DSD with Other Enzyme Deficiencies Involving the Testes But Not the Adrenal Gland -- 17,20-Lyase or Desmolase Deficiency -- 17Ý-Hydroxysteroid Dehydrogenase Type 3 -- 46, XY DSD with Disorders of Androgen Action -- 5Ü-Reductase Deficiency -- Androgen Insensitivity -- Unresponsiveness to hCG and LH -- Persistent Müllerian Duct Syndrome -- 46, XX Testicular DSD -- Anorchia or the Testicular Regression Syndrome -- Penile Agenesis -- Gonadal DSD -- Ovotesticular DSD -- 46, XY Gonadal Dysgenesis -- Endocrine Disruptors -- The Diagnosis and Treatment of Ambiguous Genitalia -- Treatment -- The Decision of Sex of Rearing -- Multidisciplinary Team Management -- Youth with Gender Dysphoria -- Suggested Readings -- 9: Disorders of Puberty -- Normal Pubertal Development -- Physical Development (Fig. 9.1) -- Age at Onset of Puberty -- Ages of Pubertal Stages and Duration -- The Pubertal Growth Spurt -- Skeletal Development and Bone Mineral Density -- The Endocrine Changes of Puberty -- Gonadarche (Fig. 9.2a) -- Spermarche -- Adrenarche -- Pediatric Sex Steroid and Gonadotropin\Assays -- Ovulation and Menarche -- Miscellaneous Metabolic Changes -- Abnormalities of Puberty -- Delayed Puberty -- Constitutional Delay in Puberty (See Chap. 5) -- Hypogonadotropic Hypogonadism (Fig. 9.2b) (#146110) -- Isolated Hypogonadotropic Hypogonadism -- Kallmann Syndrome (KS) -- Abnormalities of the Central Nervous System -- Central Nervous System Tumors -- Autoimmune or Lymphocytic Hypophysitis -- Congenital Defects of the CNS (See Chap. 3) -- Septo-optic Dysplasia -- Hypogonadotropic Hypogonadism Following Irradiation -- Idiopathic Hypopituitarism -- Syndromes Associated with Hypogonadotropic Hypogonadism -- Weight Loss and Chronic Disease -- Hypergonadotropic Hypogonadism (Fig. 9.2c) -- Disorders of the Ovaries -- Turner Syndrome
  • Other Forms of Primary Ovarian Failure
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http://library.link/vocab/discovery_link
{'f': 'http://opac.lib.rpi.edu/record=b4385196'}
Extent
1 online resource (453 pages)
Form of item
online
Isbn
9783319183718
Media category
computer
Media MARC source
rdamedia
Media type code
c
Sound
unknown sound
Specific material designation
remote

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