| Document Date: 2015-05-30 10:05:51
Open Document File Size: 127,05 KBShare Result on Facebook
City Gabow / New York / / Company CHANGE SUMMARY / Bernstein / McGraw-Hill / ketoacyl-CoA / / Event Person Communication and Meetings / / IndustryTerm medium chain / term management / oil / long chain / treatment of mitochondrial fatty acid oxidation disorders / printing / treatment of rhabdomyolysis-induced renal failure / preferred energy substrates / / MedicalCondition Nemaline myopathy / metabolic alkalosis / muscular dystrophy / recurrent myoglobinuria / Becker muscular dystrophy / McArdle disease / Debrancher deficiency / fatty acid oxidation disorders / central core disease / Muscle phosphofructokinase deficiency / Seizures / Carbon monoxide poisoning / malignant syndrome / coma / II deficiency / tachycardia / metabolic acidosis / cardiac arrhythmia / e.g. infection / contracture / Respiratory chain deficiency / inflammatory changes / Genetic Metabolic Diseases / aldolase deficiency / disorder / neuroleptic malignant syndrome / Severe Infections / Tarui disease / Heat stroke / Clinical rhabdomyolysis / Autoimmune Inflammation / acylcarnitine translocase deficiency / Central core myopathy / In vitro contracture / Myophosphorylase deficiency / myohemoglobinuric acute renal failure / Polymyositis/dermatomyositis / homocystinuria / recurrent rhabdomyolysis / Autoimmune disorders / Pyruvate kinase deficiency / kinase deficiency / acyl-CoA dehydrogenase deficiency / Management - CHW Severe Infections / Lactate dehydrogenase deficiency / Crush syndrome / cardiomyopathy / respiratory failure / Acute Rhabdomyolysis / autosomal dominant pharmacogenetic disorder / mitochondrial fatty acid oxidation disorders / shock / metabolic acidosis / Acute renal failure complicating muscle crush injury / Introduction Rhabdomyolysis / long-chain fat oxidation disorders / Phosphoglycerate mutase deficiency / Cori disease / Painful muscle contractures / rhabdomyolysis-induced renal failure / Other Genetic Disorders / fever / Rhabdomyolysis / Compartment syndrome / severe rhabdomyolysis / pain / Myoadenylate deaminase deficiency / Inherited Disease / Chen Y-T. Glycogen storage diseases / Igarashi M. Congenital muscular dystrophy / Muscular Dystrophies / infection / SLE / Inborn Errors of Metabolism / traumatic rhabdomyolysis / deficiency / X-linked adrenoleukodystrophy / Phosphoglycerate kinase deficiency / renal failure / Oxidative phosphorylation diseases / acute renal failure / recurrent acute myoglobinuria / Genetic Disorders / Glycogen storage diseases / / MedicalTreatment diet therapy / venovenous hemofiltration / dialysis / hemofiltration / / Organization Genetic Metabolic Diseases Service / GSD V / PICU / Nephrology Department / SCHN Policy / Procedure and Guideline Committee / / Person Horn F. Screening / Review Period / Ding J. Mitochondrial / Sydney Children / / Position Team Leader / Director / / Product droperidol / sodium bicarbonate / acetazolamide / halothane / / ProvinceOrState Gillingham / / PublishedMedium Journal of Clinical Investigation / / Technology dialysis / /
SocialTag |
PLEASE TYPE POLICY TITLE HERE