JIMD Reports, Volume 45

Author:   Eva Morava ,  Matthias Baumgartner ,  Marc Patterson ,  Shamima Rahman
Publisher:   Springer-Verlag Berlin and Heidelberg GmbH & Co. KG
Edition:   1st ed. 2019
Volume:   45
ISBN:  

9783662586464


Pages:   110
Publication Date:   28 January 2019
Format:   Paperback
Availability:   Manufactured on demand   Availability explained
We will order this item for you from a manufactured on demand supplier.

Our Price $232.85 Quantity:  
Add to Cart

Share |

JIMD Reports, Volume 45


Add your own review!

Overview

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.

Full Product Details

Author:   Eva Morava ,  Matthias Baumgartner ,  Marc Patterson ,  Shamima Rahman
Publisher:   Springer-Verlag Berlin and Heidelberg GmbH & Co. KG
Imprint:   Springer-Verlag Berlin and Heidelberg GmbH & Co. K
Edition:   1st ed. 2019
Volume:   45
Weight:   0.454kg
ISBN:  

9783662586464


ISBN 10:   3662586460
Pages:   110
Publication Date:   28 January 2019
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Paperback
Publisher's Status:   Active
Availability:   Manufactured on demand   Availability explained
We will order this item for you from a manufactured on demand supplier.

Table of 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.

Reviews

Author Information

Tab Content 6

Author Website:  

Customer Reviews

Recent Reviews

No review item found!

Add your own review!

Countries Available

All regions
Latest Reading Guide

ls

Shopping Cart
Your cart is empty
Shopping cart
Mailing List