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Books on the topic 'Incidentalome'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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1

Califano, Licia. Il contraddittorio nel processo costituzionale incidentale. Torino: G. Giappichelli, 2003.

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2

Il giudizio costituzionale incidentale come processo senza parti. Milano: A. Giuffrè, 1985.

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3

Ferrante, Umberto. L' appello incidentale e il procedimento camerale nell'appello penale. Milano: Giuffrè, 1991.

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4

Bonomi, Andrea. L'assorbimento dei vizi nel giudizio di costituzionalità in via incidentale. Napoli, NA, Italia: Jovene editore, 2013.

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5

Catelani, Elisabetta. La determinazione della "questione di legittimità costituzionale" nel giudizio incidentale. Milano: Giuffrè, 1993.

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6

Pignatelli, Nicola. Le "interazioni" tra processo amministrativo e processo costituzionale in via incidentale. Torino: G. Giappichelli, 2008.

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7

Vignola, Alessandra. L'intervento dei terzi nel giudizio di legittimità costituzionale in via incidentale. Torino: G. Giappichelli, 2000.

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8

Endocrine incidentalomas. Philadelphia: Saunders, 2000.

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9

Imaging Of Incidentalomas. W.B. Saunders Company, 2011.

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10

Katritsis, Demosthenes G., Bernard J. Gersh, and A. John Camm. Secondary hypertension. Oxford University Press, 2014. http://dx.doi.org/10.1093/med/9780199685288.003.0502_update_002.

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The causes of secondary hypertension and their therapy are discussed. Considered conditions are secondary hypertension, renovascular hypertension, renal parenchymal disease, primary aldosteronism, phaeochromocytoma, adrenal incidentaloma, and other causes of secondary hypertension.
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11

NIH state-of-the-science statement on management of the clinically inapparent adrenal mass ("incidentaloma"). [Bethesda, Md.]: National Institutes of Health, Office of the Director, 2002.

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12

NIH state-of-the-science statement on management of the clinically inapparent adrenal mass ("incidentaloma"). [Bethesda, Md.]: National Institutes of Health, Office of the Director, 2002.

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13

National Institutes of Health (U.S.) and NIH Consensus Development Program, eds. NIH state-of-the-science statement on management of the clinically inapparent adrenal mass ("incidentaloma"). [Bethesda, Md.]: National Institutes of Health, Office of the Director, 2002.

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14

NIH state-of-the-science statement on management of the clinically inapparent adrenal mass ("incidentaloma"). [Bethesda, Md.]: National Institutes of Health, Office of the Director, 2002.

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15

National Institutes of Health (U.S.) and NIH Consensus Development Program, eds. NIH state-of-the-science statement on management of the clinically inapparent adrenal mass ("incidentaloma"). [Bethesda, Md.]: National Institutes of Health, Office of the Director, 2002.

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16

NIH state-of-the-science statement on management of the clinically inapparent adrenal mass ("incidentaloma"). [Bethesda, Md.]: National Institutes of Health, Office of the Director, 2002.

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17

Kwon, Rachel J. Size as a Predictor of Malignancy of Adrenal Cortical Carcinoma. Edited by Randall Owen. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199384075.003.0042.

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This chapter provides a summary of a landmark study in endocrine surgery. Does size correlate with malignancy in adrenal cortical carcinoma? Starting with that question, it describes the basics of the study, including year study began, year study was published, study location, who was studied, who was excluded, how many patients, study design, study intervention, follow-up, endpoints, results, and criticism and limitations. The chapter briefly reviews other relevant studies and information, gives a summary and discusses implications, and concludes with a relevant clinical case involving postoperative treatment of a patient with adrenocortical carcinoma who has a large adrenal incidentaloma.
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18

Jolly, Elaine, Andrew Fry, and Afzal Chaudhry, eds. Endocrine. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199230457.003.0007.

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Chapter 7 covers the basic science and clinical topics relating to the endocrine system which trainees are required to learn as part of their basic training and demonstrate in the MRCP. It covers endocrine physiology, acid-base balance, thyrotoxicosis, hypothyroidism, goitre and thyroid nodule, Cushing syndrome, acromegaly, hyperprolactinaemia, hypopituitarism, diabetes insipidus, adrenal incidentaloma, primary hyperaldosteronism, adrenal insufficiency, phaeochromocytoma and paraganglioma , male hypogonadism and Gynaecomastia, menstrual disorders and anovulation, hirsutism and the polycystic ovarian syndrome, multiple endocrine neoplasia and other genetic endocrine tumour syndromes, neuroendocrine tumours, acid-base disorders, sodium disorders, potassium disorders, hypocalcaemia, hypercalcaemia, hyperparathyroidism, osteoporosis, osteomalacia, Paget disease, dyslipidaemia, porphyria, adult inborn errors of metabolism, and obesity.
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19

Bagul, A., and Saba Balasubramanian. Treatment of adrenal tumours. Edited by James W. F. Catto. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199659579.003.0095.

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The incidence of adrenal tumours has risen dramatically over the last two decades, mainly due to the incidental detection of adrenal lesions on cross sectional imaging performed for other diseases. These ‘incidentalomas’ are commoner than the well-known hormonal syndromes such as Cushing’s, Conn’s, and pheochromocytoma. Suspicion or detection of an adrenal tumour should result in a detailed biochemical and structural evaluation in a multidisciplinary setting. The relatively low incidence of adrenal disease coupled with the varied nature of presentation makes concentration of volume and encouragement of expertise difficult in this area; however, these are important as it correlates directly with outcome.
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