02520nam 2200649Ia 450 991045029100332120200520144314.01-107-12616-91-280-15980-497866101598021-139-13040-40-511-12192-X0-511-04288-40-511-14782-10-511-05466-1(CKB)1000000000001468(EBL)202167(OCoLC)171135621(SSID)ssj0000123553(PQKBManifestationID)11139386(PQKBTitleCode)TC0000123553(PQKBWorkID)10007938(PQKB)10984623(MiAaPQ)EBC202167(Au-PeEL)EBL202167(CaPaEBR)ebr10023547(CaONFJC)MIL15980(EXLCZ)99100000000000146820011002d2002 uy 0engur|n|---|||||txtccrA clinical guide to inherited metabolic diseases[electronic resource] /Joe T.R. Clarke2nd ed.Cambridge, U.K. ;New York Cambridge University Press20021 online resource (307 p.)Description based upon print version of record.0-521-89076-4 Includes bibliographical references and index.Cover; Half-title; Title; Copyright; Dedicaton; Contents; Preface; Foreword; 1 General principles; 2 Neurologic syndrome; 3 Metabolic acidosis; 4 Hepatic syndrome; 5 Cardiac syndromes; 6 Storage syndrome and dysmorphism; 7 Acute metabolic illness in the newborn; 8 Newborn screening; 9 Laboratory investigation; 10 Treatment; IndexThis clinically organized, user-friendly, handbook is intended to help general physicians and medical specialists in training with the first critical steps in clinical diagnosis: how to determine that this is an inherited metabolic disease, and where to go from here to establish a diagnosis.Metabolism, Inborn errors ofDiagnosis, DifferentialElectronic books.Metabolism, Inborn errors of.Diagnosis, Differential.616.3/9042Clarke Joe T. R987387MiAaPQMiAaPQMiAaPQBOOK9910450291003321A clinical guide to inherited metabolic diseases2256726UNINA