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Bibliographies thématiques / Endocrine abnormalities / Livres

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Livres sur le sujet « Endocrine abnormalities »

Auteur : Grafiati

Publié le 2 juin 2025

Mis à jour le 31 juillet 2025

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1

L, Gauderer Michael W., and Angerpointner Thomas, eds. Surgery for endocrinological diseases and malformations in childhood. Springer-Verlag, 1991.

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2

G, Parker Malcolm, ed. Nuclear hormone receptors: Molecular mechanisms, cellular functions, clinical abnormalities. Academic, 1991.

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3

G, Parker Malcolm, ed. Nuclear hormone receptors: Molecular mechanisms, cellular functions, and clinical abnormalities. Academic Press, 1991.

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4

John, Money. Vandalized lovemaps: Paraphilic outcome of seven cases in pediatric sexology. Prometheus Books, 1989.

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5

John, Money. Vandalized lovemaps: Paraphilic outcome of seven cases in pediatric sexology. Prometheus Books, 1989.

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6

Guggenheim, Alena. Underlying hormonal and neurotransmitter abnormalities in systemic lupus erythematous [sic]: Evidence for novel treatments in management of disease. NCNM, 2007.

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7

1934-, Brown Gregory M., Wainwright S. D. 1927-, and International Congress of Endocrinology (7th : 1984 : Quebec, Quebec), eds. The Pineal gland: Endocrine aspects : proceedings of a symposium held in conjunction with the Seventh International Endocrinology Congress, Canada, April 1984. Pergamon Press, 1985.

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8

S, Holmes Clarissa, ed. Psychoneuroendocrinology: Brain, behavior, and hormonal interactions. Springer-Verlag, 1990.

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9

Remarkables: Endocrine Abnormalities in Art. University of California Press, 2011.

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10

Menstrual Cycle: Signs and Symptoms, Psychological/Behavioral Changes and Abnormalities. Nova Science Pub Inc, 2013.

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11

Henriette A. Delemarre-van de Waal. Abnormalities In Puberty: Scientific And Clinical Advances (Endocrine Development). S. Karger AG (Switzerland), 2005.

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12

Sekhar, Rajagopal V. Endocrine Disorders. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190493097.003.0035.

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HIV infection is now a chronic disease, and it is associated with an increasing prevalence of metabolic and endocrine abnormalities. The underlying etiology of these disorders can be attributed to multiple factors, including, but not limited to, the effects of HIV itself, antiretroviral drugs, the effects of immune dysfunction, and other opportunistic infections. Any endocrine glandular system can be involved; hence, appropriate clinical suspicion, endocrinological dynamic testing for accurate diagnosis, and effective therapy are important in the identification and management of these disorder

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13

Blanshard, Hannah. Endocrine and metabolic disease. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198719410.003.0008.

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This chapter describes the anaesthetic management of the patient with endocrine and metabolic disease. Topics covered include diabetes mellitus, thyroid and parathyroid disease, acromegaly, adrenocortical disease, steroid therapy, Cushing’s and Conn’s syndromes, apudoma (including phaeochromocytoma), and abnormalities of sodium and potassium. For each topic, preoperative investigation and optimization, treatment, and anaesthetic management are described. The perioperative management of the diabetic patient is discussed in detail, including insulin and oral hypoglycaemic therapy. Perioperative

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14

Blanshard, Hannah. Endocrine and metabolic disease. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198719410.003.0008_update_001.

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This chapter describes the anaesthetic management of the patient with endocrine and metabolic disease. Topics covered include diabetes mellitus, thyroid and parathyroid disease, acromegaly, adrenocortical disease, steroid therapy, Cushing’s and Conn’s syndromes, apudoma (including phaeochromocytoma), and abnormalities of sodium and potassium. For each topic, preoperative investigation and optimization, treatment, and anaesthetic management are described. The perioperative management of the diabetic patient is discussed in detail, including insulin and oral hypoglycaemic therapy. Perioperative

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15

Soffer, Jocelyn, and Harold W. Goforth. Endocrine Comorbidities in Persons with HIV. Edited by Mary Ann Cohen, Jack M. Gorman, Jeffrey M. Jacobson, Paul Volberding, and Scott Letendre. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199392742.003.0045.

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A wide range of endocrine abnormalities commonly accompany and complicate HIV infection, many of which have implications for psychiatrists and other mental health professionals working with this population. Such abnormalities include adrenal insufficiency, hypercortisolism, hyperthyroidism, hypothyroidism, hypogonadism, decreased bone mineral density, and bone disease. Endocrinopathies are great mimickers of psychiatric disorders, manifesting in some cases as disturbances of mood, sleep, appetite, thought process, energy level, or general sense of well-being. Understanding the intricate and co

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16

Adam, Sheila, Sue Osborne, and John Welch. Endocrine, obstetric, and drug overdose emergencies. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199696260.003.0014.

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This chapter discusses specific endocrine, obstetric, and drug overdose emergencies that necessitate admission to the critical care unit. First, the underlying physiology and management of endocrine disorders such as phaeocromocytoma, Addisonian crisis, diabetic emergencies (such as diabetic ketoacidosis), thyroid disorders, and calcium abnormalities are discussed. Secondly, the physiology and management of pregnancy-related problems are discussed including hypertensive disorders of pregnancy (such as pre-eclampsia), acute fatty liver of pregnancy, peri-partum cardiomyopathy, massive obstetric

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17

Nass, MD, Ruth, and Yitzchak Frank, MD, eds. Cognitive and Behavioral Abnormalities of Pediatric Diseases. Oxford University Press, 2010. http://dx.doi.org/10.1093/oso/9780195342680.001.0001.

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This book provides a detailed account of intellectual, other neuropsychological and behavioral manifestations of general pediatric diseases. The conditions discussed include the whole range of pediatric diseases - genetic syndromes, other congenital conditions, metabolic, endocrine, gastrointestinal, infectious, immunologic, toxic, trauma, and neoplastic, as well as sensory disabilities including deafness and blindness. Although the book is not intended to discuss cognitive and behavioral manifestations of conditions usually considered to be primary neurological disease, some of those, includi

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18

Parker, Malcolm G. Nuclear Hormone Receptors: Molecular Mechanisms, Cellular Functions, Clinical Abnormalities. Academic Press, 1991.

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19

Sills, Irene N., and Martin M. Fisher, eds. AM:STARs: Advances in the Treatment of Endocrine Disorders in Adolescents, Vol. 26, No. 2. American Academy of Pediatrics, 2015. http://dx.doi.org/10.1542/9781581109498.

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There are a series of endocrine disorders that can affect adolescents, some of which are related to growth and development and others that can occur at any age but may have specific implication for the adolescent age group. This issue provides a comprehensive update of endocrine issues seen in adolescents, with a focus on recent advances in diagnosis and treatment. Contents in Advances in the Treatment of Endocrine Disorders in Adolescents include Thyroid Disorders Update on Diabetes Melitus Disorders of Growth and Puberty Bone Health in Adolescents Polycystic Ovarian Syndrome Adrenal Disorder

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20

Straub, Rainer H. Neuroendocrine system. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0022.

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Endocrine abnormalities are very common in patients with chronic autoimmune rheumatic diseases (CARDs) due to the systemic involvement of the central nervous system and endocrine glands. In recent years, the response of the endocrine (and also neuronal) system to peripheral inflammation has been linked to overall energy regulation of the diseased body and bioenergetics of immune cells. In CARDs, hormonal and neuronal pathways are outstandingly important in partitioning energy-rich fuels from muscle, brain, and fat tissue to the activated immune system. Neuroendocrine regulation of fuel allocat

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21

Straub, Rainer H. Neuroendocrine system. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199642489.003.0022_update_002.

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Endocrine abnormalities are very common in patients with chronic autoimmune rheumatic diseases (CARDs) due to the systemic involvement of the central nervous system and endocrine glands. In recent years, the response of the endocrine (and also neuronal) system to peripheral inflammation has been linked to overall energy regulation of the diseased body and bioenergetics of immune cells. In CARDs, hormonal and neuronal pathways are outstandingly important in partitioning energy-rich fuels from muscle, brain, and fat tissue to the activated immune system. Neuroendocrine regulation of fuel allocat

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22

Straub, Rainer H. Neuroendocrine system. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199642489.003.0022_update_003.

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Endocrine abnormalities are very common in patients with chronic autoimmune rheumatic diseases (CARDs) due to the systemic involvement of the central nervous system and endocrine glands. In recent years, the response of the endocrine (and also neuronal) system to peripheral inflammation has been linked to overall energy regulation of the diseased body and bioenergetics of immune cells. In CARDs, hormonal and neuronal pathways are outstandingly important in partitioning energy-rich fuels from muscle, brain, and fat tissue to the activated immune system. Neuroendocrine regulation of fuel allocat

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23

Sultan, Charles. Pediatric and Adolescent Gynecology: Evidence-Based Clinical Practice (Endocrine Development, V. 7). S. Karger Publishers (USA), 2004.

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24

Surgical correction of intersexual genitalia and female genital malformation. Springer-Verlag, 1985.

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25

Crum, Brian A., Eduardo E. Benarroch, and Robert D. Brown. Neurologic Disorders Categorized by Anatomical Involvement. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780199755691.003.0523.

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Neurological disorders of the brain, spine, and peripheral nervous system are examined. Symptoms and signs related to disorders of the cerebral cortex may lead to alterations in cognition and consciousness. Unilateral neurologic symptoms involving a single neurologic symptom commonly localize to the cerebral cortex. Abnormalities of speech and language are localized to the dominant cerebral hemisphere, whereas abnormalities of the nondominant hemisphere may lead to visuospatial deficits, confusion, or neglect of the contralateral side of the body. The hypothalamus is important in many function

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26

Holmes, Clarissa S. Psychoneuroendocrinology: Brain, Behavior, and Hormonal Interactions. Springer London, Limited, 2012.

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27

Holmes, Clarissa S. Psychoneuroendocrinology: Brain, Behavior, and Hormonal Interactions. Springer, 2011.

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28

Psychoneuroendocrinology: Brain, Behavior, and Hormonal Interactions. Springer, 2012.

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29

Hodgkiss, Andrew. Therapeutic strategies. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198759911.003.0013.

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A wide range of therapeutic strategies to manage cancer-related psychopathology are described. Evidence-based interventions include: surgery (e.g. oophorectomy for anti-NMDAR limbic encephalitis), radiotherapy, immunotherapy, anti-glucocorticoids, correction of electrolyte abnormalities, correction of vitamin or endocrine deficiencies, and the use of carefully selected antidepressant or antipsychotic medication. Particular attention is paid to the management of cancer-related delirium and mania, and to the depressive phenomena provoked by systemic cancer treatments. The quality of the evidence

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30

Litell, John M., and Nathan I. Shapiro. Pathophysiology of septic shock. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0297.

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The pathophysiology of sepsis is the result of a dysregulated host response to infection. Interactions between conserved pathogenic signals and host recognition systems initiate a systemic reaction to local infection. Pro- and anti-inflammatory intermediates and associated coagulatory abnormalities lead to altered macrovascular, microvascular, and mitochondrial function. Uncorrected, these processes yield similar patterns of failure in multiple organ systems. Mortality increases with successive organ failures. Although commonly thought to be a manifestation of impaired renal circulation, septi

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31

Dohle, Gert R. Infertility. Edited by David John Ralph. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199659579.003.0096.

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The assessment of men with fertility problems is described in this chapter. The main causes of male infertility are testicular insufficiency due to congenital and acquired causes, obstructions of the male genital tract, genetic and endocrine abnormalities, urogenital infections, and varicoceles. Lifestyle can also have a negative influence on semen quality: smoking, obesity, drugs, and anabolic steroids influence sperm parameters and may reduce natural conception. Some chronic diseases also have a negative influence on fertility. History taking and physical examination should focus on prevalen

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32

London, Gerard M. Cardiovascular complications in end-stage renal disease patients. Edited by Jonathan Himmelfarb. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0268.

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Cardiovascular complications are the predominant cause of death in patients with end-stage renal disease (ESRD). The high incidence of cardiovascular complications results from pathology present before ESRD (generalized atherosclerosis, diabetes, hypertension) and an additive effect of multiple factors including haemodynamic overload and metabolic and endocrine abnormalities more or less specific to uraemia or its treatment modalities. These disorders are usually associated and can exacerbate each other. While ischaemic heart disease is a frequent cause of cardiac death, heart failure and sudd

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33

Morava, Eva, and Mirian C. H. Janssen. Congenital Disorders of Glycosylation. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0063.

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Congenital disorders of glycosylation (CDGs) are usually diagnosed during infancy or childhood with severe multisystem disorder and neurologic presentation. With the increasing number of surviving adult patients, recognition of the distinct adult phenotype and awareness of the diagnostic difficulties in adulthood is essential. Patients with O-glycosylation defects or with abnormal dolichol synthesis might present first in adulthood. The majority of cases with adult CDG have a neurologic disease with intellectual disability, ataxia, speech disorder, visual disturbance, and skeletal findings. Ps

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34

Kennett, Robin P., and Sidra Aurangzeb. Primary muscle diseases. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199688395.003.0024.

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This chapter on primary muscle diseases explains how analysis of compound muscle action potential (CMAP) amplitude, abnormal spontaneous activity on needle electromyography (EMG), and motor unit action potentials (MUAP) characteristics may be used to give an indication of pathophysiological processes, and goes on to describe the combination and distribution of abnormalities that may be expected in the more commonly encountered myopathies. The conditions considered in detail are inflammatory myopathy (including myositis), critical illness myopathy, disorders with myotonia, inherited myopathy (i

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Martino-Andrade, Anderson J., and Shanna H. Swan. Interaction of Pharmaceuticals with Environmental Chemicals. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190490911.003.0007.

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This chapter describes research on several commonly used analgesics that have been described as endocrine-disrupting chemicals, leading to concerns about possible interactions between therapeutic drugs and chemicals in the environment. Mild analgesics such as acetaminophen are widely used by pregnant women worldwide. In vitro, in vivo, and epidemiologic studies report that prenatal exposure to acetaminophen and other mild analgesics can cause hormonal disturbances resulting in gonadal development and male genital abnormalities, particularly cryptorchidism. These results suggest the potential f

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Kevin Luk, K. H., and Deepak Sharma. Subarachnoid Hemorrhage. Edited by David E. Traul and Irene P. Osborn. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190850036.003.0024.

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Subarachnoid hemorrhage (SAH) is commonly caused by rupture of an intracranial aneurysm, arteriovenous malformation, or due to trauma. Prompt diagnosis and intervention are required to control intracranial pressure, maintain cerebral perfusion, and prevent rebleeding. Clinical grading of the bleed predicts morbidity and mortality, whereas imaging grading predicts risk of cerebral vasospasm. Hydrocephalus can occur as a result of SAH, which requires treatment with an external ventricular drain. Endovascular and open microsurgical procedures are available for securing the vascular abnormalities.

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Cooper, Mark S. Hormone therapies in critical illness. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0049.

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A range of hormonal manipulations have been proposed as adjunctive therapy during critical care. These therapies might be used to treat a pre-existing or acquired hormonal disorder. Additionally, hormonal manipulation has been suggested to alter the long-term outcome of critical illness, even in patients without structural abnormalities of endocrine glands. Currently, the effectiveness of these anabolic therapies has not been established and they might be harmful in some patient groups. Recently, it has been recognized that many critically-ill patients have low levels of vitamin D and this is

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Pediatric ICD-10-CM. American Academy of Pediatrics, 2015. http://dx.doi.org/10.1542/9781581109016.

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In this first edition, Pediatric ICD-10-CM: A Manual for Provider-Based Coding strives to bring to the pediatric provider, coder, and biller the most accurate and easy-to use manual on ICD-10-CM yet. Composed entirely with a pediatrics focus, this manual exclusively features codes and guidelines for physician- and provider-based coding, all in a simplified yet familiar format. The full draft of the ICD-10-CM code set comes in at well over 1,000 pages. This book condenses that large and potentially cumbersome book into 400 pages of the most relevant,pediatrics-related codes and guidelines. It a

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