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Practical Developments in Inherited Metabolic Disease is een boek van Springer;
Vergelijkbare producten zoals Practical Developments in Inherited Metabolic Disease: DNA Analysis, Phenylketonuria and Screening for Congenital Adrenal Hyperplasia
The study of inherited metabolic disease became a subject of more than academic interest in 1953 when Bickel, Gerrard and Hickmans dis;
Vergelijkbare producten zoals Medico-Social Management of Inherited Metabolic Disease
Congenital Adrenal Hyperplasia: A Comprehensive Guide addresses how hydrocortisone works, what can go wrong, and how to correct it;
Vergelijkbare producten zoals Congenital Adrenal Hyperplasia
Congenital Adrenal Hyperplasia (CAH) is an inherited disorder of the adrenal glands. Its effects can be wide-ranging and serious-from;
Vergelijkbare producten zoals Congenital Adrenal Hyperplasia
Congenital Adrenal Hyperplasia; Animal Models of Adrenocortical Tumorigenesis; Genetics of Adrenal Cortical Tumors; Adrenal Incidentalomas;
Vergelijkbare producten zoals Adrenal Cortical Neoplasia, An Issue of Endocrinology and Metabolism Clinics of North America
women, Risks of Testosterone Therapy in Women, Non-Classic Congenital Adrenal Hyperplasia, and more.;
Vergelijkbare producten zoals Androgens in Women: Too Much, Too Little, Just Right, An Issue of Endocrinology and Metabolism Clinics of North America
, congenital adrenal hyperplasia, and congenital hypothyroidism.;
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laboratory testing and biomarkers are an integral part in the diagnosis and treatment of inherited metabolic diseases. The book covers currently used;
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physicians in screening and identifying suspected metabolic disorders and a collection of resources for families. Features: Synthesizes;
Vergelijkbare producten zoals Inherited Metabolic Epilepsies
, Hypothyroidism, Thyroid Nodules, Thyroid Cancer, Thyroiditis, Pituitary Tumors, Pheochromocytoma, Congenital adrenal hyperplasia, Adrenal Insufficiency;
Vergelijkbare producten zoals Pregnancy and Endocrine Disorders, An Issue of Endocrinology and Metabolism Clinics of North America
research. Therefore, this book was aimed to compose current developments on metabolic diseases research for the use by broad spectrum of experts;
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approach to uncommon conditions (such as congenital adrenal hyperplasia, transgender conditions). In addition to presenting clinical insights, and;
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of adipose tissue in females, insulin sensitivity, congenital adrenal hyperplasia, and Cushing's disease/syndrome. There is also a discussion of PCOS;
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plasma and serum test for non-invasive screening, diagnostic and prognostic tests, as compared to biopsy-driven gene expression analysis, factors;
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diabetes, Turner syndrome, congenital adrenal hyperplasia, endocrine sequelae of childhood cancer, and transgender care - with condition-specific;
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Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency); Reproductive Issues for Turner Syndrome; Fertility and Reproduction Among Childhood;
Vergelijkbare producten zoals Reproductive Consequences of Pediatric Disease, An Issue of Endocrinology and Metabolism Clinics of North America
in phenylketonuria and cystic fibrosis. Both diseases provide examples of the possibilities of population screening, while in phenylketonuria an eminently;
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include Retinopathy of Prematurity, the Near-Term Infant, endocrine issues including congenital adrenal hyperplasia and ambiguous genitalia;
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that this is an inherited metabolic disease, and where one goes from here to establish a diagnosis. The well-illustrated text is organised;
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, Phenylketonuria and Canavan disease, as they are major emerging diseases in multiethnic populations.;
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need for a working knowledge of these diseases more important than ever. Inherited Metabolic Disease in Adults offers an authoritative;
Vergelijkbare producten zoals Inherited Metabolic Disease in Adults
foals and horses, magnesium disorders, equine metabolic syndrome, pars intermedia dysfunction (Cushing's disease), disorders of the hypothalamus;
Vergelijkbare producten zoals Endocrine Diseases, An Issue of Veterinary Clinics: Equine Practice
of genetic and environmental factors can lead to its failure. Inherited mutations give rise to congenital heart disease, the most common birth defect;
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analysis of complex metabolic pathways and ways of employing recombinant DNA techniques to alter cell behavior, metabolic patterns, and product;
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the genetic and protein levels have spurred this growth, opening the door for a deeper understanding of metabolic events. This in turn;
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authors review the most current information available about the work-up, diagnosis, and treatment of adult congenital heart disease, including;
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like phenylketonuria, galactosaemia and urea cycle defects is limited, scattered and not easily accessible, making the care for these patients;
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