JIMD Reports - Case and Research Reports, Volume 13 [[electronic resource] /] / edited by Johannes Zschocke, K. Michael Gibson, Garry Brown, Eva Morava, Verena Peters |
Edizione | [1st ed. 2014.] |
Pubbl/distr/stampa | Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2014 |
Descrizione fisica | 1 online resource (164 p.) |
Disciplina |
616.3/9042
616.39042 |
Collana | JIMD Reports |
Soggetto topico |
Human genetics
Metabolic diseases Pediatrics Human physiology Human Genetics Metabolic Diseases Human Physiology |
ISBN | 3-642-54149-6 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
""Contents""; ""Newborn Screening for Glutaric Aciduria-II: The New England Experience""; ""Abstract""; ""Introduction""; ""Methods and Population""; ""Results""; ""Discussion""; ""Synopsis""; ""Conflict of Interest""; ""Informed Consent/Human or Animal Studies""; ""Authors Attestations""; ""References""; ""Systematic Data Collection to Inform Policy Decisions: Integration of the Region 4 Stork (R4S) Collaborative Newborn Screening...""; ""Abstract""; ""Introduction""; ""Washington Newborn Screening""; ""Analyte Selection and Review""; ""Cutoff Determinations""; ""Post-Analytical Tools""
""Limitations""""Conclusion""; ""Synopsis""; ""Compliance with Ethics Guidelines""; ""Conflict of Interest""; ""Animal Rights and Human Subjects""; ""Details of the Contributions of Individual Authors""; ""References""; ""Application of a Second-Tier Newborn Screening Assay for C5 Isoforms""; ""Abstract""; ""Introduction""; ""Case Report""; ""Materials and Methods""; ""Results""; ""Discussion""; ""Compliance with Ethics Guidelines""; ""Details of the Contributions of Individual Authors""; ""References""; ""Cystinosis with Sclerotic Bone Lesions""; ""Abstract""; ""Case Report""; ""Discussion"" ""Conclusion""""Conflict of Interest""; ""Informed Consent""; ""Contributions of the Individual Authors""; ""References""; ""Pregnancy and Lactation Outcomes in a Turkish Patient with Lysinuric Protein Intolerance""; ""Abstract""; ""Introduction""; ""Case Report""; ""Discussion""; ""Take-Home Message""; ""Compliance with Ethical Guidelines""; ""References""; ""Adult-Onset Fatal Neurohepatopathy in a Woman Caused by MPV17 Mutation""; ""Abstract""; ""Case Report""; ""Discussion""; ""Summary""; ""Compliance with Ethics Guidelines""; ""References"" ""Multiple Acyl-CoA Dehydrogenation Deficiency (Glutaric Aciduria Type II) with a Novel Mutation of Electron Transfer Flavoprote...""""Abstract""; ""Introduction""; ""Materials and Methods""; ""Subject""; ""Diet Loading Test""; ""GC-MS Analysis""; ""LC-MS/MS Analysis""; ""Cell Culture""; ""RT-PCR""; ""PCR-Restriction Fragment Length Polymorphism (PCR-RFLP)""; ""Results""; ""Feline MADD""; ""Sequencing of Feline ETFα, ETFbeta, and ETFDH""; ""Presence of a Novel Mutation in the Cat with MADD""; ""Discussion""; ""Synopsis""; ""Compliance with Ethics Guidelines""; ""References"" ""Biotin-Responsive Basal Ganglia Disease: A Treatable Differential Diagnosis of Leigh Syndrome""""Abstract""; ""Introduction""; ""Case Report""; ""Discussion""; ""Synopsis""; ""Compliance with Ethics Guidelines""; ""Conflict of Interest""; ""Informed Consent""; ""Animal Rights""; ""References""; ""Severe Hypertriglyceridemia in a Newborn with Monogenic Lipoprotein Lipase Deficiency: An Unconventional Therapeutic Approach ...""; ""Abstract""; ""Introduction""; ""Materials and Methods""; ""Patient""; ""Exchange Transfusion (ET) Procedure""; ""Analysis of LPL Gene""; ""Results"" ""ET Procedure and Follow-Up"" |
Record Nr. | UNINA-9910300343303321 |
Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2014 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
JIMD Reports Volume 16 [[electronic resource] /] / edited by Johannes Zschocke, K. Michael Gibson, Garry Brown, Eva Morava, Verena Peters |
Edizione | [1st ed. 2014.] |
Pubbl/distr/stampa | Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2014 |
Descrizione fisica | 1 online resource (113 p.) |
Disciplina |
599935
610 611.01816 612 616.39 618.92 |
Collana | JIMD Reports |
Soggetto topico |
Human genetics
Metabolic diseases Pediatrics Human physiology Human Genetics Metabolic Diseases Human Physiology |
ISBN | 3-662-44587-5 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Contents; Leucine Loading Test is Only Discriminative for 3-Methylglutaconic Aciduria Due to AUH Defect; Abstract; Introduction; Material and Methods; Patients; Leucine Loading Tests; Urinary Organic Acid Analysis; Leucine Loading Tests in Patients Described in the Literature; Results; Discussion; Disclosures; Compliance with Ethics Guidelines; Conflict of Interest; Informed Consent; Details of the Contributions of Individual Authors; References; Fabry Disease: Multidisciplinary Evaluation After 10 Years of Treatment with Agalsidase Beta; Abstract; Introduction; Objective
Materials and MethodsStatistical Analysis; Results; Discussion; Conclusions; Take-Home Message; Compliance with Ethics Guidelines; Conflict of Interest; Informed Consent; Details of the Contributions of Individual Authors; References; Chondroitin 6-Sulfate as a Novel Biomarker for Mucopolysaccharidosis IVA and VII; Abstract; Introduction; Materials and Method; Subjects; Chemicals and Materials; Sample Preparation; Apparatus; Method Validation; Statistical Analysis; Results; LC-MS/MS Conditions; Calibration Curves; Precision and Accuracy; Chondroitin 6-Sulfate (C6S) Levels Keratan Sulfate (KS) LevelCorrelation Between KS and C6S Levels; Discussion; Compliance with Ethics Guidelines; Conflict of Interest; Informed Consent; Animal Rights; Contributions to the Project; References; Carnitine Profile and Effect of Suppletion in Children with Renal Fanconi Syndrome due to Cystinosis; Abstract; Background; Patients and Methods; Results; Discussion; Synopsis; Compliance with Ethics Guidelines; Conflict of Interest; Informed Consent; Details of the Contributions of Individual Authors; References Cognitive and Antipsychotic Medication Use in Monoallelic GBA-Related Parkinson DiseaseAbstract; Introduction; Methods; Data Collection; Statistical Analysis; Results; Discussion; Sources of Support; Synopsis Sentence; Compliance with Ethics Guidelines; Conflict of Interest; Other Disclosures; Informed Consent; Animal Rights; Individual Author Contributions; Guarantor; References; Laronidase Replacement Therapy and Left Ventricular Function in Mucopolysaccharidosis I; Abstract; Introduction; Case Report; Methods; Conventional, Pulse Doppler, and Speckle Tracking Echocardiograms Statistical AnalysisResults; Clinical Findings After LRT; Echocardiographic Findings After LRT; Relation of LV Weight to Urinary Uronic Acid Concentration, Diastolic Function, and Contraction Synchrony; Discussion; Limitations; Funding; Disclosure; Synopsis; Compliance with Ethics Guidelines; Conflict of Interest; Informed Consent; Animal Rights; Author Contributions; Competing Interests; Funding; References; Fibrolamellar Hepatocellular Carcinoma Mimicking Ornithine Transcarbamylase Deficiency; Abstract; Introduction; Case Report; Discussion; Synopsis Details of the Contributions of Individual Authors |
Record Nr. | UNINA-9910300341103321 |
Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2014 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
JIMD Reports, Volume 14 [[electronic resource] /] / edited by Johannes Zschocke, K. Michael Gibson, Garry Brown, Eva Morava, Verena Peters |
Edizione | [1st ed. 2014.] |
Pubbl/distr/stampa | Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2014 |
Descrizione fisica | 1 online resource (116 p.) |
Disciplina |
599935
610 611.01816 612 616.39 618.92 |
Collana | JIMD Reports |
Soggetto topico |
Human genetics
Metabolic diseases Pediatrics Human physiology Human Genetics Metabolic Diseases Human Physiology |
ISBN | 3-662-43748-1 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Contents; Molecular Analysis of Turkish Maroteaux-Lamy Patients and Identification of One Novel Mutation in the Arylsulfatase B (ARSB) G...; Abstract; Introduction; Materials and Methods; Patients; ARSB Mutation Analysis; Sequence Variations Nomenclature; Analysis of the New Missense Sequence Variation; Results; Genotype-Phenotype Correlation; Family Studies; Discussion; One-Sentence Take-Home Message; Details of the Contributions of Individual Authors; Name of One Author Who Serves as Guarantor; Details of Funding; Details of Ethics Approval; A Patient Consent Statement; Conflict of Interest
ReferencesDanon Disease Due to a Novel LAMP2 Microduplication; Abstract; Introduction; Methods; Results; Discussion; Acknowledgments; Synopsis; Compliance with Ethics Guidelines; Author Contributions; References; Secondary Mitochondrial Respiratory Chain Defect Can Delay Accurate PFIC2 Diagnosis; Abstract; Introduction; Case Reports; Discussion; One-Sentence Take-Home Message; Contribution of Individual Authors; References; Newborn Screening for Hunter Disease: A Small-Scale Feasibility Study; Abstract; Introduction; Materials and Methods; DBS Samples; Enzyme Assay; Results and Discussion ConclusionConflict of Interest; Informed Consent; Details of the Contributions of Individual Authors; References; Abnormalities in Glycogen Metabolism in a Patient with Alpers´ Syndrome Presenting with Hypoglycemia; Abstract; Introduction; Case Report; Discussion; Competing Interest; Synopsis; Compliance with Ethics Guidelines; Conflict of Interest; Informed Consent; Animal Rights; Contributions of Individual Authors; References; Assessment of Basal Metabolic Rate and Nutritional Status in Patients with Gaucher Disease Type III; Abstract; Introduction; Methods; Results; Basal Metabolic Rate Nutritional StatusDiscussion; Conclusion; Summary; References; Mutations in the Complex III Assembly Factor Tetratricopeptide 19 Gene TTC19 Are a Rare Cause of Leigh Syndrome; Abstract; Introduction; Conclusions; Compliance with Ethics Guidelines; Informed Consent; References; Quality of Life in Adult Patients with Glycogen Storage Disease Type I: Results of a Multicenter Italian Study; Abstract; Introduction; Methods; Statistical Analysis; Results; Discussion; Conclusions; Compliance with Ethics Guidelines; References The Molecular Bases of Phenylketonuria (PKU) in New South Wales, Australia: Mutation Profile and Correlation with Tetrahydrobi...Abstract; Introduction; Materials and Methods; Results; Discussion; Conflict of Interest; Synopsis; Compliance with Ethics Guidelines; Details of Contributions of Individual Authors; References; Extraosseous Extension Caused by Epidural Hematoma in Gaucher Disease Mimicking Malignant Bone Tumor; Abstract; Introduction; Case Report; Discussion; Conflict of Interest; Informed Consent; Contributions of Individual Authors; References Thirteen Patients with MAT1A Mutations Detected Through Newborn Screening: 13 Years´ Experience |
Record Nr. | UNINA-9910300066603321 |
Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2014 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
JIMD Reports, Volume 15 [[electronic resource] /] / edited by Johannes Zschocke, K. Michael Gibson, Garry Brown, Eva Morava, Verena Peters |
Edizione | [1st ed. 2015.] |
Pubbl/distr/stampa | Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2015 |
Descrizione fisica | 1 online resource (133 p.) |
Disciplina | 616.39042 |
Collana | JIMD Reports |
Soggetto topico |
Human genetics
Metabolic diseases Pediatrics Human physiology Human Genetics Metabolic Diseases Human Physiology Genètica humana Trastorns del metabolisme Pediatria Fisiologia humana |
Soggetto genere / forma | Llibres electrònics |
ISBN | 3-662-43751-1 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
""Contents""; ""4-Hydroxyglutamate Is a Biomarker for Primary Hyperoxaluria Type 3""; ""Abstract""; ""Introduction""; ""Materials and Methods""; ""Results""; ""Assay Performance""; ""4OHGlu Levels in Controls and PH3 Families""; ""Discussion""; ""Compliance with Ethics Guidelines""; ""Author Contributions""; ""Conflicts of Interest""; ""Ethical Approval""; ""References""; ""Excellent Response to a Ketogenic Diet in a Patient with Alternating Hemiplegia of Childhood""; ""Abstract""; ""Introduction""; ""Patient and Methods""; ""Procedure""; ""Results""; ""Discussion""; ""Synopsis""
""Compliance with Ethics and Guidelines""""Conflict of Interest""; ""Informed Consent""; ""Animal Rights""; ""Details of the Contributions of Individual Authors""; ""References""; ""Thiamine-Responsive and Non-responsive Patients with PDHC-E1 Deficiency: A Retrospective Assessment""; ""Abstract""; ""Introduction""; ""Methods""; ""Results""; ""Discussion""; ""Compliance with Ethics Guidelines""; ""Conflict of Interest""; ""Details of the Contributions of Individual Authors""; ""References"" ""Diagnostic Exome Sequencing and Tailored Bioinformatics of the Parents of a Deceased Child with Cobalamin Deficiency Suggests ...""""Abstract""; ""Introduction""; ""Subjects and Methods""; ""Results""; ""Discussion""; ""Compliance with Ethics Guidelines""; ""Synopsis""; ""Conflict of Interest""; ""Informed Consent""; ""Animal Rights""; ""Details of the Contributions of Individual Authors""; ""Electronic-Database Information""; ""References""; ""Report of Two Never Treated Adult Sisters with Aromatic l-Amino Acid Decarboxylase Deficiency: A Portrait of the Natural Histo...""; ""Abstract"" ""Introduction""""Patients""; ""Patient 1 (Fig.1; II-3)""; ""Patient 2 (Fig.1; II-4)""; ""Biochemical Phenotype and Genotype""; ""Treatments""; ""Discussion""; ""Compliance with Ethics Guidelines""; ""Synopsis""; ""Conflict of Interest""; ""Ethics Approval""; ""PatientÂ?s Informed Consent""; ""Animal Rights""; ""AuthorsÂ? Contribution""; ""References""; ""Lysine-Restricted Diet as Adjunct Therapy for Pyridoxine-Dependent Epilepsy: The PDE Consortium Consensus Recommendations""; ""Abstract""; ""Introduction""; ""Methods""; ""Results""; ""Literature Search"" ""Pharmacotherapy: Recommendation""""Add-on Dietary Treatment: General Recommendations and Rationale""; ""Recommendations (Fig.2)""; ""Rationale""; ""Diet Prescriptions (See Online Supplement for More Details)""; ""Nutritional Aims""; ""Diet Management in (Breastfed) Infants""; ""Assessment of Lysine Content""; ""Lysine-Free Amino Acid Formulas""; ""Monitoring""; ""Clinical Monitoring""; ""Biochemical and Routine Laboratory Monitoring""; ""Nutritional Markers""; ""Neurological Monitoring""; ""Neurodevelopmental Monitoring""; ""Neuro-Radiological Monitoring""; ""Emergency Treatment"" ""Discussion"" |
Record Nr. | UNINA-9910300209903321 |
Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2015 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
JIMD Reports, Volume 17 [[electronic resource] /] / edited by Johannes Zschocke, K. Michael Gibson, Garry Brown, Eva Morava, Verena Peters |
Edizione | [1st ed. 2014.] |
Pubbl/distr/stampa | Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2014 |
Descrizione fisica | 1 online resource (95 p.) |
Disciplina | 616.39042 |
Collana | JIMD Reports |
Soggetto topico |
Human genetics
Metabolic diseases Pediatrics Human physiology Human Genetics Metabolic Diseases Human Physiology |
ISBN | 3-662-44578-6 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
""Contents""; ""Reversible Keratopathy Due to Hypertyrosinaemia Following Intermittent Low-Dose Nitisinone in Alkaptonuria: A Case Report""; ""Abstract""; ""Introduction""; ""Case Report""; ""Discussion""; ""Compliance with Ethics Guidelines""; ""Contribution from Authors""; ""References""; ""Sports in LCHAD Deficiency: Maximal Incremental and Endurance Exercise Tests in a 13-Year-Old Patient with Long-Chain 3-Hydrox...""; ""Abstract""; ""Introduction""; ""Case Report""; ""Applied Tests (Methods)""; ""Results""; ""Standard Incremental Cycle Test""; ""Standard Endurance Cycle Test""
""Anaerobic Threshold, Maximal Lactate Steady State (MLSS)""""Metabolic Laboratory Tests""; ""Discussion""; ""Compliance with Ethical Standards""; ""Conflict of Interest""; ""Informed Consent""; ""References""; ""A Hunter Patient with a Severe Phenotype Reveals Two Large Deletions and Two Duplications Extending 1.2Mb Distally to IDS Locus""; ""Abstract""; ""Introduction""; ""Materials and Methods""; ""Results""; ""Clinical Description""; ""Array CGH Analysis""; ""Discussion""; ""Conclusion""; ""One Sentence Take-Home Message""; ""Details of the contributions of individual authors"" ""Name of one author who serves as guarantor""""Details of funding""; ""Details of ethics approval""; ""A patient consent statement""; ""Conflict of interest""; ""References""; ""Widening Phenotypic Spectrum of AADC Deficiency, a Disorder of Dopamine and Serotonin Synthesis""; ""Abstract""; ""Introduction""; ""Case Reports""; ""Discussion""; ""Synopsis""; ""Compliance with Ethics Guidelines""; ""References""; ""Antiepileptic Medications Increase Osteoporosis Risk in Male Fabry Patients: Bone Mineral Density in an Australian Cohort""; ""Abstract""; ""Introduction""; ""Methods"" ""Study Population""""Dual X-Ray Absorptiometry""; ""Biochemistry""; ""Statistical Analysis""; ""Results""; ""Study Population""; ""Dual X-Ray Absorptiometry""; ""Biochemistry""; ""Patient Outcomes""; ""Discussion""; ""Take-Home Message""; ""Compliance with Ethics Guidelines""; ""Details of Contributions of Individual Authors""; ""Conflict of Interest""; ""Informed Consent""; ""References""; ""The Complexity of Newborn Screening Follow-Up in Phenylketonuria""; ""Abstract""; ""Introduction""; ""Clinical Report""; ""Discussion""; ""Synopsis""; ""Compliance with Ethics Guidelines"" ""Conflict of Interest""""Informed Consent and Animal Rights""; ""References""; ""Revised Proposal for the Prevention of Low Bone Mass in Patients with Classic Galactosemia""; ""Abstract""; ""Introduction""; ""Diagnostic Procedures""; ""Dietary Evaluation and Bone Metabolism Markers""; ""Estrogen Supplementation""; ""Physical Activity Evaluation""; ""Assessment of Spinal Deformities""; ""Dual-Energy X-Ray Absorptiometry""; ""Follow-Up and Therapeutic Interventions""; ""Dietary Evaluation and Bone Metabolism Markers""; ""Estrogen Supplementation""; ""Physical Activity Evaluation"" ""Assessment of Spinal Deformities"" |
Record Nr. | UNINA-9910300350803321 |
Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2014 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|