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JIMD Reports, Volume 44 de Eva Morava

JIMD Reports, Volume 44: JIMD Reports, cartea 44

Editat de Eva Morava, Matthias Baumgartner, Marc Patterson, Shamima Rahman, Johannes Zschocke, Verena Peters
en Limba Engleză Paperback – 15 ian 2019
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: 9783662586167
ISBN-10: 3662586169
Pagini: 119
Ilustrații: VI, 119 p. 32 illus., 22 illus. in color.
Dimensiuni: 210 x 279 mm
Greutate: 0.3 kg
Ediția:1st ed. 2019
Editura: Springer Berlin, Heidelberg
Colecția Springer
Seria JIMD Reports

Locul publicării:Berlin, Heidelberg, Germany

Cuprins

A Homozygous Splice Site Mutation in SLC25A42, Encoding the Mitochondrial Transporter of Coenzyme A, Causes Metabolic Crises and Epileptic Encephalopathy.- Apparent Acetaminophen Toxicity in a Patient with Transaldolase Deficiency.- Sialuria: Ninth Patient Described Has a Novel Mutation in GNE.- Stability of the ABCD1 Protein with a Missense Mutation: A Novel Approach to Finding Therapeutic Compounds for X-Linked Adrenoleukodystrophy.- Psychosocial Functioning in Parents of MPS III Patients.- The Second Case of Saposin A Deficiency and Altered Autophagy.- An Electronic Questionnaire for Liver Assessment in Congenital Disorders of Glycosylation (LeQCDG): A Patient-Centered Study.- Demographics, Clinical Features, and Mortality of Acute Hepatic Porphyrias in Colombia: An Analysis of 101 Patients.- Cobalamin D Deficiency Identified Through Newborn Screening.- Lathosterolosis: A Relatively Mild Case with Cataracts and Learning Difficulties.- DPAGT1 Deficiency with Encephalopathy (DPAGT1-CDG): Clinical and Genetic Description of 11 New Patients.- Enzyme Replacement Therapy During Pregnancy in Fabry Patients.- Hyperornithinemia, Hyperammonemia, and Homocitrullinuria Syndrome Causing Severe Neonatal Hyperammonemia.- Screening for Niemann-Pick Type C Disease in a Memory Clinic Cohort.- Reversible Cerebral White Matter Abnormalities in Homocystinuria.

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