Detalles del Título
Detalles del Título

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Título Clinical studies in medical biochemistry. - Tercera edición.Libros / Impreso - Libros
Autor(es) Glew, Robert H. (Editor)
Rosenthal, Miriam D. (Editor)
Publicación New York, NY : Oxford University Press, 2007
Descripción Física xiv, 373 páginas : ilustraciones ; 26 cm.
Idioma Inglés;
ISBN 019517688X
Clasificación(es) 612.015
QUIMICA
Materia(s) Bioquímica clínica - Estudio de casos; Bioquímica; Técnicas y procedimientos de laboratorio; Enfermedades metabólicas;
Nota(s) Incluye referencias bibliográficas e índice
CONTENIDO: Nucleic acids and protein structure and function. Fragile X syndrome -- Sickle cell anemia -- Osteogenesis imperfecta -- a1-Antitrypsin deficiency -- Cardiac troponin: clinical role in the diagnosis of myocardial infarction -- Hereditary spherocytosis -- Fuel metabolism and energetics. Pyruvate dehydrogenase complex deficiency -- Mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): a case of mitochondrial disease -- Systemic carnitine deficiency: a treatable disorder -- Neonatal hypoglycemia and the importance of gluconeogenesis -- Intermediary metabolism. Glucose 6-phosphate dehydrogenase deficiency and oxidative hemolysis -- Biotinidase deficiency: a biotin-responsive disorder -- Adrenoleukodystrophy -- Low-density lipoprotein receptors and familial hypercholesterolemia -- Tangier disease: a disorder in the reverse cholesterol transport pathway -- Gaucher disease: a sphingolipidosis -- I-cell disease (Mucolipidosis II) -- Inborn errors of urea synthesis -- Phenylketonuria -- HMG-CoA lyase deficiency -- Hyperhomocysteinemia -- Neonatal hyperbilirubinemia -- Digestion, absorption, and nutritional biochemistry. Obesity: a growing problem -- Protein-energy malnutrition -- Lactose intolerance -- Pancreatic insufficiency secondary to chronic pancreatitis -- Abetalipoproteinemia -- Vitamin B12 deficiency -- Vitamin A deficiency in children -- Calcium-deficiency rickets -- Hereditary hemochromatosis -- Endocrinology and integration of metabolism. Type I diabetes mellitus -- Congenital adrenal hyperplasia: P450c21 steroid hydroxylase deficiency.
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Disponibilidad
CodBarras Localización Piso Signatura Estado Categoría
104879Biblioteca Universidad Icesi2612.015/C641cDisponibleCol. General