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JIMD Reports, Volume 45 / edited by Eva Morava, Matthias Baumgartner, Marc Patterson, Shamima Rahman, Johannes Zschocke, Verena Peters.

SpringerLink Books Biomedical and Life Sciences 2019 Available online

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Format:
Book
Contributor:
Morava, Eva, editor.
Baumgartner, Matthias, 1865- editor.
Patterson, Marc, editor.
Rahman, Shamima, editor.
Zschocke, Johannes, editor.
Peters, Verena, editor.
SpringerLink (Online service)
Series:
Biomedical and Life Sciences (Springer-11642)
JIMD reports 2192-8304 ; 45.
JIMD Reports, 2192-8304 ; 45
Language:
English
Subjects (All):
Human genetics.
Metabolism--Disorders.
Metabolism.
Pediatrics.
Medicine.
Human Genetics.
Metabolic Diseases.
Molecular Medicine.
Local Subjects:
Human Genetics.
Metabolic Diseases.
Pediatrics.
Molecular Medicine.
Physical Description:
1 online resource (VI, 110 pages) : 28 illustrations, 13 illustrations in color.
Contained In:
Springer eBooks
Place of Publication:
Berlin, Heidelberg : Springer Berlin Heidelberg : Imprint: Springer, 2019.
System Details:
text file PDF
Summary:
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.
Contents:
I-Cell Disease (Mucolipidosis II): A Case Series from a Tertiary Paediatric Centre Reviewing the Airway and Respiratory Consequences of the Disease
Oral Ganglioside Supplement Improves Growth and Development in Patients with Ganglioside GM3 Synthase Deficiency
Feeding Difficulties and Orofacial Myofunctional Disorder in Patients with Hepatic Glycogen Storage Diseases
Auxiliary Partial Orthotopic Liver Transplantation for Monogenic Metabolic Liver Diseases: Single-Centre Experience
A Novel Truncating FLAD1 Variant, Causing Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in an 8-Year-Old Boy
The Effect of Continuous Intravenous Glucagon on Glucose Requirements in Infants with Congenital Hyperinsulinism
Case of Neonatal Fatality from Neuromuscular Variant of Glycogen Storage Disease Type IV
Acute and Chronic Management in an Atypical Case of Ethylmalonic Encephalopathy
Dihydropyrimidine Dehydrogenase Deficiency: Homozygosity for an Extremely Rare Variant in DPYD due to Uniparental Isodisomy of Chromosome 1
Severe Neonatal Manifestations of Infantile Liver Failure Syndrome Type 1 Caused by Cytosolic Leucine-tRNA Synthetase Deficiency
Enzyme Replacement Therapy in Pregnant Women with Fabry Disease: A Case Series
Survival of a Male Infant with a Familial Xp11.4 Deletion Causing Ornithine Transcarbamylase Deficiency
The Unique Spectrum of Mutations in Patients with Hereditary Tyrosinemia Type 1 in Different Regions of the Russian Federation
Elevated Lyso-Gb3 Suggests the R118C GLA Mutation Is a Pathological Fabry Variant
Glycogen Storage Disease Type IV: A Rare Cause for Neuromuscular Disorders or Often Missed?
A Hemizygous Deletion Within the PGK1 Gene in Males with PGK1 Deficiency.
Other Format:
Printed edition:
ISBN:
978-3-662-58647-1
9783662586471
Access Restriction:
Restricted for use by site license.

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