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Genetic diagnosis of endocrine disorders /

Genetic diagnosis of endocrine disorders, Second edition provides users with a comprehensive reference that is organized by endocrine grouping (i.e., thyroid, pancreas, parathyroid, pituitary, adrenal, and reproductive and bone), discussing the genetic and molecular basis for the diagnosis of variou...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Weiss, Roy E. (Editor ), Refetoff, Samuel (Editor )
Formato: Electrónico eBook
Idioma:Inglés
Publicado: London : Academic Press is an imprint of Elsevier, [2016]
Edición:Second edition.
Temas:
Acceso en línea:Texto completo

MARC

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020 |a 9780128008928  |q (electronic bk.) 
020 |a 012800892X  |q (electronic bk.) 
020 |z 9780128008928  |q (hardcover) 
020 |z 012800892X  |q (hardcover) 
035 |a (OCoLC)921886444  |z (OCoLC)1066431692 
050 4 |a RC648 
060 4 |a WK 140 
082 0 4 |a 616.4042  |2 23 
245 0 0 |a Genetic diagnosis of endocrine disorders /  |c edited by Roy E. Weiss, Samuel Refetoff. 
250 |a Second edition. 
264 1 |a London :  |b Academic Press is an imprint of Elsevier,  |c [2016] 
264 4 |c �2016 
300 |a 1 online resource (xv, 433 pages) :  |b illustrations (some color) 
336 |a text  |b txt  |2 rdacontent 
336 |a still image  |b sti  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
500 |a Revised edition of: Genetic diagnosis of endocrine disorders / edited by Roy E. Weiss, Samuel Refetoff. 1st ed. 2010. 
504 |a Includes bibliographical references. 
505 0 |a Mechanisms of mutation -- A clinical guide to monogenic diabetes -- Hypoglycemia -- Functioning pituitary adenomas -- Diabetes insipidus -- States of pituitary hypofunction -- Congenital defects of thyroid hormone synthesis -- Developmental abnormalities of the thyroid -- Syndromes of impaired sensitivity to thyroid hormone -- Molecular diagnosis of thyroid cancer -- Genetics of hyperparathyroidism including parathyroid cancer -- Genetic diagnosis of skeletal dysplasias -- Vitamin d disorders -- Congenital adrenal hyperplasia -- Genetics of adrenocortical tumors (ACT) and hypersecretory syndromes -- Hereditary syndromes involving pheochromocytoma and paraganglioma -- Genetic conditions associated with congenital adrenocortical insufficiency or glucocorticoid and/or mineralocorticoid resistance -- Genetic considerations in the evaluation of menstrual cycle irregularities -- Disorders of sex development -- Androgen insensitivity due to mutations of the androgen receptor -- Obesity -- Syndromes of severe insulin resistance and/or lipodystrophy -- Lipodystrophies -- Multiple endocrine neoplasia type 1 (MEN1) -- Genetics of polyglandular failure -- Genetic diagnosis of growth failure -- Cost-effectiveness of genetic testing for monogenic diabetes -- Genetic counseling: the role of genetic counselors on healthcare provider and endocrinology teams -- Setting up a laboratory -- Introduction to applications of genomic sequencing. 
520 |a Genetic diagnosis of endocrine disorders, Second edition provides users with a comprehensive reference that is organized by endocrine grouping (i.e., thyroid, pancreas, parathyroid, pituitary, adrenal, and reproductive and bone), discussing the genetic and molecular basis for the diagnosis of various disorders. The book emphasizes the practical nature of diagnosing a disease, including which tests should be done for the diagnosis of diabetes mellitus in adults and children, which genes should be evaluated for subjects with congenital hypothyroidism, which genetic tests should be ordered in obese patients or for those with parathyroid carcinoma, and the rationale behind testing for multiple endocrine neoplasias. 
588 0 |a Online resource; title from resource home page (ClinicalKey, viewed May 10, 2017). 
650 0 |a Endocrine glands  |x Diseases  |x Genetic aspects. 
650 0 |a Endocrine glands  |x Diseases  |x Diagnosis. 
650 0 |a Endocrine glands  |x Diseases  |x Treatment. 
650 0 |a Genetic screening. 
650 1 2 |a Endocrine System Diseases  |x genetics  |0 (DNLM)D004700Q000235 
650 1 2 |a Endocrine System Diseases  |x diagnosis  |0 (DNLM)D004700Q000175 
650 2 2 |a Genetic Testing  |0 (DNLM)D005820 
650 2 2 |a Molecular Diagnostic Techniques  |0 (DNLM)D025202 
650 6 |a Glandes endocrines  |0 (CaQQLa)201-0009870  |x Maladies  |0 (CaQQLa)201-0009870  |x Aspect g�en�etique.  |0 (CaQQLa)201-0377534 
650 6 |a Glandes endocrines  |0 (CaQQLa)201-0009870  |x Maladies  |0 (CaQQLa)201-0009870  |x Traitement.  |0 (CaQQLa)201-0377521 
650 6 |a D�epistage g�en�etique.  |0 (CaQQLa)201-0074873 
650 7 |a Genetic screening  |2 fast  |0 (OCoLC)fst00940094 
650 7 |a Endocrine glands  |x Diseases  |x Diagnosis  |2 fast  |0 (OCoLC)fst00909730 
650 7 |a Endocrine glands  |x Diseases  |x Genetic aspects  |2 fast  |0 (OCoLC)fst00909731 
650 7 |a Endocrine glands  |x Diseases  |x Treatment  |2 fast  |0 (OCoLC)fst00909735 
655 4 |a Internet Resources. 
700 1 |a Weiss, Roy E.,  |e editor. 
700 1 |a Refetoff, Samuel,  |e editor. 
730 0 |i Preceded by:  |a Genetic diagnosis of endocrine disorders.  |s 1st ed. 
776 0 8 |i Print version:  |t Genetic diagnosis of endocrine disorders.  |b Second edition.  |d Amsterdam : Elsevier/Academic Press, [2016]  |z 9780128008928  |w (OCoLC)948243144 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/book/9780128008928  |z Texto completo