Over 10 mio. titler Fri fragt ved køb over 499,- Hurtig levering Forlænget returret til 31/01/25

Biomarkers in Inborn Errors of Metabolism

- Clinical Aspects and Laboratory Determination

  • Format
  • Bog, hardback
  • Engelsk

Beskrivelse

Biomarkers of Inborn Errors in Metabolism: Clinical Aspects and Laboratory Determination is structured around the new reality that laboratory testing and biomarkers are an integral part in the diagnosis and treatment of inherited metabolic diseases. The book covers currently used biomarkers as well as markers that are in development. Because biomarkers used in the initial diagnosis of disease may be different than the follow-up markers, the book also covers biomarkers used in both the prognosis and treatment of inherited metabolic disorders. With the introduction of expanded new-born screening for inborn metabolic diseases, an increasing numbers of laboratories are involved in follow-up confirmatory testing. The book provides guidance on laboratory test selection and interpreting results in patients with suspected inherited metabolic diseases. The book provides comprehensive guidance on patient diagnosis and follow-up through its illustrative material on metabolic pathways, genetics and pathogenesis, treatment and prognosis of inherited metabolic diseases, along with essential information on clinical presentation. Each chapter is organized with a uniform, easy-to-follow format: a brief description of the disorder and pathway; a description of treatment; biomarkers for diagnosis; biomarkers followed for treatment efficacy; biomarkers followed for disease progression; confounding conditions that can either: affect biomarker expression or mimic IEMs; other biomarkers: less established, future.

Læs hele beskrivelsen
Detaljer
Størrelse og vægt
  • Vægt1130 g
  • coffee cup img
    10 cm
    book img
    19,1 cm
    23,5 cm

    Findes i disse kategorier...

    Se andre, der handler om...

    Biotin Diagnosis Gene therapy Immunodeficiency Dystonia Gout Dopamine Copper Biochemical markers Manganese Amino acids Mitochondria Creatine Adenosine Ataxia Endoplasmic reticulum Glycosaminoglycans Molybdenum Galactose Intellectual Disability Fructose Adenosine monophosphate Monoamines Cofactors Liver disease Biomarkers Fatty acid oxidation Glycogen Genetic diagnosis Mitochondrial myopathy Mucopolysaccharidoses Inborn errors of metabolism Enzyme replacement therapy Mitochondrial disease Catabolism Fatty acid oxidation disorders Cobalamin Lactic acidosis Guanine Heparan sulfate 3-methylcrotonyl ABCD transporters Acyl-CoA thioesterases Acylglycines Adenine orotic acid AICA-ribotide AGAT AMN (adrenomyeloneuropathy) And ptosis syndrome (NARP) Acylcarnitine Acylcarnitines Arginine-glycine amidinotransferase Alpers-Huttenlocher syndrome (AHS) Aminoacidopathies carbohydrate metabolism Biotinidase De novo pathway Dietary modification Dolichol Dihydrothymine Carnitine transport Cerebrosides Dihydroorotic acid Dihydrouracil electron transport chain Encephalomyopathy Congenital disorders of glycosylation Ether lipid Guanosine Creatine transporter Hematopoietic stem cell therapy (HSCT) Glutaric acid GAMT Gangliosides and sulfatides Deoxyadenosine Dermatan sulfate Inosine Infantile Refsum disease (IRD) Guanidinoacetate Inosine Monophosphate Leber's hereditary optic neuropathy (LHON) Maternally inherited diabetes-deafness syndrome (MIDD) Mitochondrial neurogastrointestinal encephalopathy syndrome (MNGIE) Mannose Method evaluation Globosides Mitochondrial DNA (mtDNA) Guanidinoacetate methyltransferase Myoclonic epilepsy with ragged red fibers syndrome (MERRF) Guanosine monophosphate hypoxanthine inherited metabolic disorders Keratan sulfate Leigh syndrome (LS) Hyperammonemia Isovaleric acid Menkes disease Kearns-Sayre syndrome (KSS) Mass spectrometry/LC-MS/MS methylmalonic acid
    Machine Name: SAXO081