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Thomas Opladen (1974-)

Arzt

Name	Thomas Opladen
Time	1974- (Date of birth and death)
Place	Bergisch Gladbach (Geburtsort) Heidelberg (Wirkungsort) Deutschland
Academic degree	PD Dr. med.
Profession	Arzt (characteristic profession)
Related	Klinikum Heidelberg
Further information	Oberarzt, Abteilung Allg. Pädiatrie, Neuropädiatrie, Stoffwechsel, Gastroenterologie, Nephrologie, Zentrum für Kinder- und Jugendmedizin, Universitätsklinikum Heidelberg
Record type	Person
GND-Identifier	124489656
Record ID	124489656
Involved in show all Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder An AI-based segmentation and analysis pipeline for high-field MR monitoring of cerebral organoids Phenotypic correlates of structural and functional protein impairments resultant from ALDH5A1 variants Erratum zu: Die intrazerebrale Gentherapie des Aromatischen-L-Aminosäure-Decarboxylase-Mangels mit Eladocagene exuparvovec. Eine Stellungnahme der Gesellschaft für Neuropädiatrie (GNP), der Arbeitsgemeinschaft pädiatrischer Stoffwechselstörungen (APS), der Deutschen Gesellschaft für Neurochirurgie (DGNC) und der Deutschen Gesellschaft für Kinder- und Jugendmedizin (DGKJ) Volumetric study of brain MRI in a cohort of patients with neurotransmitter disorders Gene therapy in the putamen for curing AADC deficiency and Parkinson's disease Die intrazerebrale Gentherapie des Aromatischen-L-Aminosäure-Decarboxylase-Mangels mit Eladocagene exuparvovec : Eine Stellungnahme der Gesellschaft für Neuropädiatrie (GNP), der Arbeitsgemeinschaft pädiatrischer Stoffwechselstörungen (APS), der Deutschen Gesellschaft für Neurochirurgie (DGNC) und der Deutschen Gesellschaft für Kinder- und Jugendmedizin (DGKJ) U-IMD: the first Unified European registry for inherited metabolic diseases One test for all: whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver–Russell syndrome Die intrazerebrale Gentherapie des Aromatischen-L-Aminosäure-Decarboxylase-Mangels mit Eladocagene exuparvovec : Eine Stellungnahme der Gesellschaft für Neuropädiatrie (GNP), der Arbeitsgemeinschaft pädiatrischer Stoffwechselstörungen (APS), der Deutschen Gesellschaft für Neurochirurgie (DGNC) und der Deutschen Gesellschaft für Kinder- und Jugendmedizin (DGKJ) One test for all : whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver–Russell syndrome Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies Ermittlung von Kerninhalten der ärztlichen Weiterbildung zum Facharzt/-ärztin der Pädiatrie mittels Delphi-Methode Inherited Disorders of Neurotransmitters: Classification and Practical Approaches for Diagnosis and Treatment Induced pluripotent stem cells (iPSCs) as model to study inherited defects of neurotransmission in inborn errors of metabolism Human heterologous liver cells transiently improve hyperammonemia and ureagenesis in individuals with severe urea cycle disorders Consensus guideline for the diagnosis and treatment of aromatic l-amino acid decarboxylase (AADC) deficiency Folinic acid therapy in cerebral folate deficiency: marked improvement in an adult patient Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders Impact of clinical exomes in neurodevelopmental and neurometabolic disorders Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers Phenylalanine loading in pediatric patients with dopa-responsive dystonia: revised test protocol and pediatric cutoff values Untersuchung zu Veränderungen der Lymphozytensubpopulationen im Krankheitsverlauf der Mukoviszidose Untersuchung zu Veränderungen der Lymphozytensubpopulationen im Krankheitsverlauf der Mukoviszidose

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Katalog der Deutschen Nationalbibliothek

Thomas Opladen (1974-)

Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder

An AI-based segmentation and analysis pipeline for high-field MR monitoring of cerebral organoids

Phenotypic correlates of structural and functional protein impairments resultant from ALDH5A1 variants

Volumetric study of brain MRI in a cohort of patients with neurotransmitter disorders

Gene therapy in the putamen for curing AADC deficiency and Parkinson's disease

U-IMD: the first Unified European registry for inherited metabolic diseases

One test for all: whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver–Russell syndrome

One test for all : whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver–Russell syndrome

Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies

Ermittlung von Kerninhalten der ärztlichen Weiterbildung zum Facharzt/-ärztin der Pädiatrie mittels Delphi-Methode

Inherited Disorders of Neurotransmitters: Classification and Practical Approaches for Diagnosis and Treatment

Induced pluripotent stem cells (iPSCs) as model to study inherited defects of neurotransmission in inborn errors of metabolism

Human heterologous liver cells transiently improve hyperammonemia and ureagenesis in individuals with severe urea cycle disorders

Consensus guideline for the diagnosis and treatment of aromatic l-amino acid decarboxylase (AADC) deficiency

Folinic acid therapy in cerebral folate deficiency: marked improvement in an adult patient

Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders

Impact of clinical exomes in neurodevelopmental and neurometabolic disorders

Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision

Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders

Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers

Phenylalanine loading in pediatric patients with dopa-responsive dystonia: revised test protocol and pediatric cutoff values

Untersuchung zu Veränderungen der Lymphozytensubpopulationen im Krankheitsverlauf der Mukoviszidose

Untersuchung zu Veränderungen der Lymphozytensubpopulationen im Krankheitsverlauf der Mukoviszidose