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  • 1
    Online Resource
    Online Resource
    Berlin, Heidelberg :Springer Berlin / Heidelberg,
    Keywords: Pediatrics. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (126 pages)
    Edition: 1st ed.
    ISBN: 9783662482278
    Series Statement: JIMD Reports ; v.24
    DDC: 616.39042
    Language: English
    Note: Intro -- Contents -- Part I Reports on Alkaptonuria -- Analysis of HGD Gene Mutations in Patients with Alkaptonuria from the United Kingdom: Identification of Novel Mutations -- Abstract -- Introduction -- Material and Methods -- Subjects -- Mutation Analysis of the HGD Gene -- Results and Discussion -- Conclusion -- Compliance with Ethics Guidelines -- Informed Consent -- Details of the Contributions of Individual Authors -- References -- Metabolic Effects of Increasing Doses of Nitisinone in the Treatment of Alkaptonuria -- Abstract -- Introduction -- Methods -- Patient Enrollment -- Sample Storage -- Sample Preparation -- Sample Acquisition Methods -- Statistical Analysis -- Results -- HGA in Urine -- Tyrosine and NTBC in Plasma -- Untargeted Metabolomics Analysis -- Patient Symptoms -- Discussion -- Synopsis -- Compliance with Ethics Guidelines -- Conflicts of Interest -- Informed Consent -- Author Contributions -- References -- Relationship Between Serum Concentrations of Nitisinone and Its Effect on Homogentisic Acid and Tyrosine in Patients with Alka... -- Abstract -- Introduction -- Materials and Methods -- Patients -- Study Design and Treatments -- Measurements -- Calculations and Statistics -- Results -- Demographics -- Nitisinone Pharmacokinetics -- Relationship Between Nitisinone Exposure and the Effect on HGA and Tyrosine -- Discussion -- Synopsis (Take-Home Message) -- Compliance with Ethics Guidelines -- Conflict of Interest -- Contributors -- References -- Investigating the Robustness and Diagnostic Potential of Extracellular Matrix Remodelling Biomarkers in Alkaptonuria -- Abstract -- Introduction -- Methods -- Clinical Cohort -- Measurements -- Robustness Analysis -- Creatinine Assessment -- Assessment of HGA Interference with Hydroxyperoxidase-Based ELISAs -- Results -- Robustness Analysis of the Biomarkers. , Interference of HGA with Enzyme-Based Assays -- Diagnostic Markers of ECM Remodelling in AKU -- Discussion -- Conclusions -- Synopsis -- Compliance with Ethics Guidelines -- Conflict of Interests -- Informed Consent -- Details of the Contributions of Individual Authors -- References -- Age-Related Deviation of Gait from Normality in Alkaptonuria -- Abstract -- Introduction -- Participants and Methods -- Results -- Discussion -- Conclusions -- Take-Home Message -- Compliance with Ethics Guidelines -- Conflict of interests -- Informed Consent -- Contributions of Individual Authors -- References -- Nitisinone Arrests but Does Not Reverse Ochronosis in Alkaptonuric Mice -- Abstract -- Introduction -- Materials and Methods -- Mice -- Sample Preparation -- Chromatographic Conditions -- Midlife Nitisinone Treatment -- Nitisinone Dose-Response -- Histological Analysis -- Quantification of Pigmented Chondrons -- Statistical Analyses -- Results -- Discussion -- Synopsis -- Compliance with Ethics Guidelines -- Conflicts of Interest -- Animal Rights -- Author Contributions -- References -- The Pigment in Alkaptonuria Relationship to Melanin and Other Coloured Substances: A Review of Metabolism, Composition and Che... -- Abstract -- Introduction -- Background -- Melanins -- Melanin Types -- Biosynthetic Pathways of Eumelanin and Pheomelanin -- Pigmentation in AKU: The Nature of the Pigment -- Analysis/Detection of the Melanin Types -- Analysis of Pigment Derived from HGA -- Compliance with Ethics Guidelines -- Conflict of Interest -- References -- Part II Case and Research Reports -- Serum GDF15 Levels Correlate to Mitochondrial Disease Severity and Myocardial Strain, but Not to Disease Progression in Adult ... -- Abstract -- Introduction -- Methods -- Patients -- GDF15 -- Medical Ethical Approval -- Myocardial Strain Measurement -- Statistics -- Results. , Patient Characteristics -- The Value of GDF15 as an Indicator of Clinical Disease Severity -- Covariates for the Concentration of GDF15 -- The Value of GDF15 in Predicting Clinical Disease Progression -- Myocardial Strain -- Family-Matched Controls -- Discussion -- Take-Home Message -- Conflict of Interest -- Informed Consent -- Details of the Contributions of Authors -- References -- Novel Genetic Mutations in the First Swedish Patient with Purine Nucleoside Phosphorylase Deficiency and Clinical Outcome Afte... -- Abstract -- Introduction -- Patient -- Investigations -- Genetic and Enzymatic Analysis -- Transplantation -- Engraftment and Immunological Reconstitution -- Posttransplant Morbidity -- Neurological Development -- Literature Review -- Discussion -- Conclusion -- Synopsis -- Compliance with Ethics Guidelines -- Informed Consent -- Author Contributions -- Conflict of Interest -- References -- CSF 5-Methyltetrahydrofolate Serial Monitoring to Guide Treatment of Congenital Folate Malabsorption Due to Proton-Coupled Fol... -- Abstract -- Introduction -- Case Report -- Results -- Discussion -- Conclusion -- Compliance with Ethics Guidelines -- Conflict of Interest: -- Informed Consent -- References -- A Novel Catastrophic Presentation of X-Linked Adrenoleukodystrophy -- Abstract -- Introduction -- Case Presentation -- Discussion -- Conclusion -- Synopsis -- Compliance with Ethics Guidelines -- Conflict of Interest -- Informed Consent -- Author Contributorship Statement -- References -- High Incidence of Biotinidase Deficiency from a Pilot Newborn Screening Study in Minas Gerais, Brazil -- Abstract -- Introduction -- Methods -- DNA Sequencing -- Results -- Discussion -- Synopsis -- Compliance with Ethics Guidelines -- Conflict of Interest -- Informed Consent -- Details of the Contributions of Individual Authors -- References. , Dopamine-Responsive Growth-Hormone Deficiency and Central Hypothyroidism in Sepiapterin Reductase Deficiency -- Abstract -- Introduction -- Case Summary -- History and Examination -- Treatment and Follow-Up -- Discussion -- Conclusion -- Synopsis -- References to Electronic Databases -- Competing Interest Statement -- Details of Contributions of Individual Authors -- Name of One Author Who Serves as Guarantor -- Ethical Approval -- References -- Clinical Findings and Natural History in Ten Unrelated Families with Juvenile and Adult GM1 Gangliosidosis -- Abstract -- Introduction -- Patients and Methods -- Results -- Discussion -- Conclusions -- Synopsis -- Compliance with Ethics Guidelines -- Conflict of Interest Statement -- Informed Consent -- Animal Rights -- Details of Author Contributions -- References -- High Incidence of Serologic Markers of Inflammatory Bowel Disease in Asymptomatic Patients with Glycogen Storage Disease Type ... -- Abstract -- Background -- Methods -- Results -- Discussion -- Conclusions -- Synopsis -- Compliance with Ethics Guidelines -- Conflict of Interest -- Informed Consent -- Details of the Contributions of Individual Authors -- References.
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  • 2
    Keywords: Medicine ; Biomedicine ; Medicine ; Human genetics ; Molecular biology ; Metabolic diseases ; Pediatrics ; Human genetics ; Molecular biology ; Metabolic diseases ; Pediatrics ; Metabolism, Inborn Errors ; Periodical
    Description / Table of Contents: 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
    Type of Medium: Online Resource
    Pages: Online-Ressource (VI, 129 p, online resource)
    Edition: Springer eBook Collection. Biomedical and Life Sciences
    ISBN: 9783662580813
    Series Statement: JIMD Reports 41
    Language: English
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  • 3
    Keywords: Medicine ; Biomedicine ; Human genetics ; Molecular biology ; Metabolic diseases ; Pediatrics ; Metabolism, Inborn Errors ; Periodical
    Description / Table of Contents: 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. The chapter 'Open-Label Single-Sequence Crossover Study Evaluating Pharmacokinetics, Efficacy, and Safety of Once-Daily Dosing of Nitisinone in Patients with Hereditary Tyrosinemia Type 1 (HT-1)' is open access under a CC BY 4.0 license via link.springer.com
    Type of Medium: Online Resource
    Pages: Online-Ressource (VI, 105 p. 20 illus., 7 illus. in color, online resource)
    ISBN: 9783662566107
    Series Statement: JIMD Reports 38
    Language: English
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  • 4
    Keywords: Medicine ; Biomedicine ; Human genetics ; Molecular biology ; Metabolic diseases ; Pediatrics ; Metabolism, Inborn Errors ; Periodical
    Description / Table of Contents: 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
    Type of Medium: Online Resource
    Pages: Online-Ressource (VI, 116 p. 20 illus., 8 illus. in color, online resource)
    ISBN: 9783662575772
    Series Statement: JIMD Reports 39
    Language: English
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  • 5
    Keywords: Medicine ; Medicine ; Human genetics ; Human genetics ; Metabolic diseases ; Pediatrics ; Human Genetics ; Metabolic diseases ; Pediatrics ; Molecular biology. ; Metabolism, Inborn Errors ; Periodical
    Description / Table of Contents: 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
    Type of Medium: Online Resource
    Pages: Online-Ressource (VI, 124 p. 35 illus., 20 illus. in color, online resource)
    Edition: Springer eBook Collection. Biomedical and Life Sciences
    ISBN: 9783662586143
    Series Statement: JIMD Reports 43
    Language: English
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  • 6
    Keywords: Medicine ; Medicine ; Human genetics ; Human genetics ; Metabolic diseases ; Pediatrics ; Human Genetics ; Metabolic diseases ; Pediatrics ; Molecular biology. ; Metabolism, Inborn Errors ; Periodical
    Description / Table of Contents: 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
    Type of Medium: Online Resource
    Pages: Online-Ressource (VI, 119 p. 32 illus., 22 illus. in color, online resource)
    Edition: Springer eBook Collection. Biomedical and Life Sciences
    ISBN: 9783662586174
    Series Statement: JIMD Reports 44
    Language: English
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  • 7
    Keywords: Medicine ; Medicine ; Human genetics ; Human genetics ; Metabolic diseases ; Pediatrics ; Human Genetics ; Metabolic diseases ; Pediatrics ; Molecular biology. ; Metabolism, Inborn Errors ; Periodical
    Description / Table of Contents: 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
    Type of Medium: Online Resource
    Pages: Online-Ressource (VI, 119 p. 18 illus., 12 illus. in color, online resource)
    Edition: Springer eBook Collection. Biomedical and Life Sciences
    ISBN: 9783662583654
    Series Statement: JIMD Reports 42
    Language: English
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  • 8
    Online Resource
    Online Resource
    Berlin, Heidelberg : Springer Berlin Heidelberg
    Keywords: Medicine ; Biomedicine ; Medicine ; Human genetics ; Molecular biology ; Metabolic diseases ; Pediatrics ; Human genetics ; Molecular biology ; Metabolic diseases ; Pediatrics ; Metabolism, Inborn Errors ; Periodical
    Description / Table of Contents: 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
    Type of Medium: Online Resource
    Pages: Online-Ressource (VI, 103 p. 20 illus., 13 illus. in color, online resource)
    Edition: Springer eBook Collection. Biomedical and Life Sciences
    ISBN: 9783662578803
    Series Statement: JIMD Reports 40
    Language: English
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  • 9
    Keywords: Medicine ; Medicine ; Human genetics ; Human genetics ; Metabolic diseases ; Pediatrics ; Human Genetics ; Metabolic diseases ; Pediatrics ; Molecular biology. ; Metabolism, Inborn Errors ; Periodical
    Description / Table of Contents: 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
    Type of Medium: Online Resource
    Pages: Online-Ressource (VI, 110 p. 28 illus., 13 illus. in color, online resource)
    Edition: Springer eBook Collection. Biomedical and Life Sciences
    ISBN: 9783662586471
    Series Statement: JIMD Reports 45
    Language: English
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