04506nam a22005415i 4500001001800000003000900018005001700027007001500044008004100059020003700100024003500137050001600172072001600188072002300204072001500227245012900242250001800371264007500389300006700464336002600531337002600557338003600583347002400619505145200643520110802095650002903203650003403232650003403266650002503300650003103325650003003356650002903386650003303415650003003448650002503478650003203503700008103535700008903616710003403705773002603739776003603765776003603801776003603837856004603873912001403919912001403933999001703947978-3-031-58819-8DE-He21320251030113255.0cr nn 008mamaa241101s2024 sz | s |||| 0|eng d a97830315881989978-3-031-58819-87 a10.1007/978-3-031-58819-82doi 4aRB155-155.8 7aMFN2bicssc 7aMED1070002bisacsh 7aMFN2thema10aLaboratory Guide to the Methods in Biochemical Geneticsh[electronic resource] /cedited by Nenad Blau, Frédéric M. Vaz. a2nd ed. 2024. 1aCham :bSpringer International Publishing :bImprint: Springer,c2024. aXVII, 533 p. 177 illus., 86 illus. in color.bonline resource. atextbtxt2rdacontent acomputerbc2rdamedia aonline resourcebcr2rdacarrier atext filebPDF2rda0 aLaboratory Strategies in Biochemical Genetics -- Quality Control and Quality Assurance in the Biochemical Genetic Laboratory -- Simple Metabolic Screening Tests -- Lactate, Pyruvate, Acetoacetate and 3-Hydroxybutyrate -- Amino Acids -- Homocysteine, S-adenosylmethionine and S-adenosylhomocysteine -- GABA, Homocarnosine, and ?-Alanine -- Pipecolic Acid -- Organic Acids -- Acylcarnitines, Including In Vitro Loading Tests -- Plasmalogens and Polyunsaturated Fatty Acids -- Very-Long-Chain Fatty Acids and Phytanic Acid -- Oxalate, Glycolate, Glycerate, Sulfate, and Citrate -- Glycerol and Glycerol Phosphates -- Biotinidase -- Mitochondrial Respiratory Chain -- Mucopolysaccharides -- Oligosaccharides -- Sialic Acid -- Glycosphingolipids -- Congenital Disorders of Glycosylation -- Enzymes and Metabolites of Carbohydrate Metabolism -- Polyols -- Diagnosis of Inherited Defects of Cholesterol Biosynthesis -- Lipoproteins -- Genetic Disorders of Steroid Metabolism Diagnosed by Mass Spectrometry -- Bile Acids -- Pterins andRelated Enzymes -- Biogenic Amines -- Folates -- Screening for Disorders of Purine and Pyrimidine Metabolism Using HPLC-Electrospray Tandem Mass Spectrometry -- Creatine and its Metabolites -- Porphyrins, Porphobilinogen, and ?-Aminolevulinic Acid -- Trimethylaminuria -- A Tandem Mass Spectrometry Primer for Metabolite Disease Detection -- Molecular Genetics: Mutation Analysis in the Diagnosis of Metabolic Disorders. aNow in its 2nd edition, this manual describes laboratory methodology for the diagnosis of inherited metabolic diseases. The book describes a spectrum of tests, from simple screening methods via classical methods that are operational in most (if not all) biochemical laboratories, to analytical methods that depend on technologies that very few are currently employing in their labs, but are certainly the functional techniques in a biochemical laboratory in this post-genomics era. Each chapter is sufficiently detailed to be self-contained, thus enabling laboratory specialists to adopt the method in their own laboratory and obviating the need for additional methods or references. The second updated edition of the book is unique in that it is the first of its kind to be published in the last 13 years, and individual chapters have been developed by experts in the field citing both established and cutting-edge (omics) technology. Thus, it is an indispensable resource for researchers and clinicians working on the field of inherited metabolic diseases and those interested in laboratory diagnoses. 0aMedical genetics.964976 0aClinical biochemistry.967825 0aMetabolismxDisorders.978415 0aBiochemistry.965465 0aMedicinexResearch.962598 0aBiologyxResearch.96562914aMedical Genetics.96497624aMedical Biochemistry.96782824aMetabolic Disease.97841724aBiochemistry.96546524aBiomedical Research.9656331 aBlau, Nenad.eeditor.4edt4http://id.loc.gov/vocabulary/relators/edt9869261 aVaz, Frédéric M.eeditor.4edt4http://id.loc.gov/vocabulary/relators/edt9869272 aSpringerLink (Online service)0 tSpringer Nature eBook08iPrinted edition:z978303158818108iPrinted edition:z978303158820408iPrinted edition:z978303158821140uhttps://doi.org/10.1007/978-3-031-58819-8 aZDB-2-SBL aZDB-2-SXB c64660d64660