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Produktbild: JIMD Reports, Volume 35
Band 35

JIMD Reports, Volume 35

Aus der Reihe JIMD Reports

Fr. 138.00

inkl. gesetzl. MwSt., Versandkostenfrei

Beschreibung

Produktdetails

Einband

Taschenbuch

Erscheinungsdatum

20.09.2017

Abbildungen

VI, 117 p. 20 illus., 10 illus. in color.

Herausgeber

Eva Morava + weitere

Verlag

Springer Berlin

Seitenzahl

117

Maße (B/H)

21/27.9 cm

Gewicht

323 g

Auflage

1st ed. 2017

Sprache

Englisch

ISBN

978-3-662-55832-4

Beschreibung

Produktdetails

Einband

Taschenbuch

Erscheinungsdatum

20.09.2017

Abbildungen

VI, 117 p. 20 illus., 10 illus. in color.

Herausgeber

Verlag

Springer Berlin

Seitenzahl

117

Maße (B/H)

21/27.9 cm

Gewicht

323 g

Auflage

1st ed. 2017

Sprache

Englisch

ISBN

978-3-662-55832-4

Herstelleradresse

Springer-Verlag GmbH
Heidelberger Platz 3
14197 Berlin
Deutschland
Email: sdc-bookservice@springer.com
Url: www.springer.com
Telephone: +49 30 827870
Fax: +49 30 8214091

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  • Produktbild: JIMD Reports, Volume 35
  • Cerebrotendinous Xanthomatosis Presenting with Infantile Spasms and Intellectual Disability .- Hyperammonemia as a Presenting Feature in Two Siblings with  FBXL4  Variants .- Intracranial Hypertension in Cystinosis Is a Challenge: Experience in a Children’s Hospital .- Severe Respiratory Acidosis in Status Epilepticus as a Possible Etiology of Sudden Death in Lesch–Nyhan Disease: A Case Report and Review of the Literature .- Vitamin B 12  Administration by Subcutaneous Catheter Device in a Cobalamin A (cblA) Patient .- Expansion of the Phenotypic Spectrum of Propionic Acidemia with Isolated Elevated Propionylcarnitine .- Previously Unreported Biallelic Mutation in  DNAJC19: Are Sensorineural Hearing Loss and Basal Ganglia Lesions Additional Features of Dilated Cardiomyopathy and Ataxia (DCMA) Syndrome? .- Lysosomal Storage Disorders in Nonimmune Hydrops Fetalis (NIHF): An Indian Experience .- The Risk of Fatty Acid Oxidation Disorders and Organic Acidemias in Children with Normal Newborn Screening .- Clinical and Mutational Characterizations of Ten Indian Patients with Beta-Ketothiolase Deficiency .- Atypical Presentation and Treatment Response in a Child with Familial Hypercholesterolemia Having a Novel LDLR Mutation .- Development of a Tandem Mass Spectrometry Method for Rapid Measurement of Medium- and Very-Long-Chain Acyl-CoA Dehydrogenase Activity in Fibroblasts .- Analysis of Melanin-like Pigment Synthesized from Homogentisic Acid, with or without Tyrosine, and Its Implications in Alkaptonuria .- Bone Health in Classic Galactosemia: Systematic Review and Meta-Analysis .- Cognitive Development in a Young Child with Mucolipidosis Type IV: A Case Report .- White Matter Microstructure and Subcortical Gray Matter Structure Volumes in Aspartylglucosaminuria; a 5-Year Follow-up Brain MRI Study of an Adolescent with Aspartylglucosaminuria and His Healthy Twin Brother .- Erratum to: White Matter Microstructure and Subcortical Gray Matter Structure Volumes in Aspartylglucosaminuria; a 5-Year Follow-up Brain MRI Study of an Adolescent with Aspartylglucosaminuria and His Healthy Twin Brother.