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JIMD Reports, Volume 27 de Eva Morava

JIMD Reports, Volume 27: JIMD Reports, cartea 27

Editat de Eva Morava, Matthias Baumgartner, Marc Patterson, Shamima Rahman, Johannes Zschocke, Verena Peters
en Limba Engleză Paperback – 17 mai 2016
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
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Specificații

ISBN-13: 9783662504086
ISBN-10: 3662504081
Pagini: 112
Ilustrații: VI, 112 p. 28 illus., 14 illus. in color.
Dimensiuni: 210 x 279 x 6 mm
Greutate: 0.29 kg
Ediția:1st ed. 2016
Editura: Springer Berlin, Heidelberg
Colecția Springer
Seria JIMD Reports

Locul publicării:Berlin, Heidelberg, Germany

Cuprins

DetailedBiochemical and Bioenergetic Characterization of FBXL4-Related Encephalomyopathic Mitochondrial DNA Depletion.- RecurrentVentricular Tachycardia in Medium-Chain Acyl-Coenzyme A DehydrogenaseDeficiency.- Applicationof an Image Cytometry Protocol for Cellular and Mitochondrial Phenotyping on Fibroblastsfrom Patients with Inherited Disorders.- SUCLA2N-Glycosylation GalactoseIncorporation Ratios for the Monitoring of Classical Galactosaemia.- IntracranialPressure Monitoring Demonstrates that Cerebral Edema Is Not Correlated to Hyperammonemiain a Child with Ornithine Transcarbamylase Deficiency.- NoEvidence for Association of SCO2Heterozygosity with High-Grade Myopia or Other Diseases with PossibleMitochondrial Dysfunction.- VoluntaryExercise Prevents Oxidative Stress in the Brain of Phenylketonuria Mice.- SeizuresDue to a KCNQ2 Mutation: Treatmentwith Vitamin B6.- TheFrequencies of Different Inborn Errors of Metabolism in Adult MetabolicCentres: Report from the SSIEM Adult Metabolic Physicians Group.- ElectroclinicalFeatures of Early-Onset Epileptic Encephalopathies in Congenital Disorders of Glycosylation(CDGs).- TheNewborn Screening Paradox: Sensitivity vs. Overdiagnosis in VLCAD Deficiency.- FurtherDelineation of the ALG9-CDG Phenotype.

Textul de pe ultima copertă

JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.

Caracteristici

Unique collection of case and research reports on rare metabolic disorders Contains unusual or previously unrecorded features relevant to metabolic disorders All contributions rigorously peer-reviewed