JIMD Reports, Volume 31 /
| Corporate Author: | |
|---|---|
| Other Authors: | , , , , , | 
| Format: | eBook | 
| Language: | English | 
| Published: | 
      Berlin, Heidelberg :
        Springer Berlin Heidelberg : Imprint: Springer,
    
      2017.
     | 
| Edition: | 1st ed. 2017. | 
| Series: | JIMD Reports,
              31             | 
| Subjects: | 
                Table of Contents: 
            
                  - Living with Intoxication-Type Inborn Errors of Metabolism: A Qualitative Analysis of Interviews with Paediatric Patients and Their Parents
 - Switch from Sodium Phenylbutyrate to Glycerol Phenylbutyrate Improved Metabolic Stability in an Adolescent with Ornithine Transcarbamylase Deficiency
 - Inherited Metabolic Disorders: Efficacy of Enzyme Assays on Dried Blood Spots for the Diagnosis of Lysosomal Storage Disorders
 - Parent Coping and the Behavioural and Social Outcomes of Children Diagnosed with Inherited Metabolic Disorders
 - Sleep Disturbance, Obstructive Sleep Apnoea and Abnormal Periodic Leg Movements: Very Common Problems in Fabry Disease
 - Spurious Elevation of Multiple Urine Amino Acids by Ion-Exchange Chromatography in Patients with Prolidase Deficiency
 - Quick Diagnosis of Alkaptonuria by Homogentisic Acid Determination in Urine Paper Spots
 - Mitochondrial Complex III Deficiency with Ketoacidosis and Hyperglycemia Mimicking Neonatal Diabetes
 - Diagnosis, Treatment, and Clinical Outcome of Patients with Mitochondrial Trifunctional Protein/Long-Chain 3-Hydroxy Acyl-CoA Dehydrogenase Deficiency
 - N-Acetylcysteine Therapy in an Infant with Transaldolase Deficiency Is Well Tolerated and Associated with Normalization of Alpha Fetoprotein Levels
 - Severe Cardiomyopathy as the Isolated Presenting Feature in an Adult with Late-Onset Pompe Disease: A Case Report
 - Chronic Diarrhea in l-Amino Acid Decarboxylase (AADC) Deficiency: A Prominent Clinical Finding Among a Series of Ten French Patients
 - Hyperammonemia due to Adult-Onset N-Acetylglutamate Synthase Deficiency
 - Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?
 - Disease Heterogeneity in Na+/Citrate Cotransporter Deficiency
 - Erratum to: Disease Heterogeneity in Na+/Citrate Cotransporter Deficiency.