JIMD Reports, Volume 27 (eBook, PDF)
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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.

Produktbeschreibung
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.

Dieser Download kann aus rechtlichen Gründen nur mit Rechnungsadresse in A, B, BG, CY, CZ, D, DK, EW, E, FIN, F, GB, GR, HR, H, IRL, I, LT, L, LR, M, NL, PL, P, R, S, SLO, SK ausgeliefert werden.

  • Produktdetails
  • Verlag: Springer-Verlag GmbH
  • Erscheinungstermin: 05.05.2016
  • Englisch
  • ISBN-13: 9783662504093
  • Artikelnr.: 46924707
Inhaltsangabe
Detailed
Biochemical and Bioenergetic Characterization of FBXL4 -Related Encephalomyopathic Mitochondrial DNA Depletion.- Recurrent
Ventricular Tachycardia in Medium-Chain Acyl-Coenzyme A Dehydrogenase
Deficiency.- Application
of an Image Cytometry Protocol for Cellular and Mitochondrial Phenotyping on Fibroblasts
from Patients with Inherited Disorders.- SUCLA2 N -Glycosylation Galactose
Incorporation Ratios for the Monitoring of Classical Galactosaemia.- Intracranial
Pressure Monitoring Demonstrates that Cerebral Edema Is Not Correlated to Hyperammonemia
in a Child with Ornithine Transcarbamylase Deficiency.- No
Evidence for Association of SCO2
Heterozygosity with High-Grade Myopia or Other Diseases with Possible
Mitochondrial Dysfunction.- Voluntary
Exercise Prevents Oxidative Stress in the Brain of Phenylketonuria Mice.- Seizures
Due to a KCNQ2 Mutation: Treatment
with Vitamin B 6 .- The
Frequencies of Different Inborn Errors of Metabolism in Adult Metabolic
Centres: Report from the SSIEM Adult Metabolic Physicians Group.- ElectroclinicalFeatures of Early-Onset Epileptic Encephalopathies in Congenital Disorders of Glycosylation
(CDGs).- The
Newborn Screening Paradox: Sensitivity vs. Overdiagnosis in VLCAD Deficiency.- Further
Delineation of the ALG9-CDG Phenotype.