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Baroque: Figures of Excess in Seventeenth-Century European Art and German Literature

Burgard, Peter J

1, 2019

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Impact of glycogen storage disease type I on adult daily life: a survey

Orphanet journal of rare diseases, 2021-09, Vol.16 (1), p.1-371, Article 371

2021

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Efficacy and outcome of expanded newborn screening for metabolic diseases--report of 10 years from South-West Germany

Orphanet journal of rare diseases, 2011-06, Vol.6 (1), p.44-44, Article 44

2011

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Impact of Diagnosis and Therapy on Cognitive Function in Urea Cycle Disorders

Annals of neurology, 2019-07, Vol.86 (1), p.116-128

2019

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William L. Nyhan, Georg F. Hoffmann. Atlas of inherited metabolic diseases (Hardcover and e‐Book) 4th ed. Boca Raton: CRC Press, Taylor & Francis Group, 2020, 855 p., $175; £120, €124. ISBN‐13: 9781138196599. (With contributions from Aida I. Al‐Aqeel and Bruce A. Barshop)

Journal of inherited metabolic disease, 2021-01, Vol.44 (1), p.284-284

Burgard, Peter

2021

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An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Federal Joint Committee

Orphanet journal of rare diseases, 2021-11, Vol.16 (1), p.474-474, Article 474

2021

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Transition for adolescents with a rare disease: results of a nationwide German project

Orphanet journal of rare diseases, 2023-04, Vol.18 (1), p.93-93, Article 93

2023

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High blood pressure, a red flag for the neonatal manifestation of urea cycle disorders

Orphanet journal of rare diseases, 2019-04, Vol.14 (1), p.80-80, Article 80

2019

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Long-term outcome in methylmalonic acidurias is influenced by the underlying defect (mut0, mut- , cblA, cblB)

Pediatric research, 2007-08, Vol.62 (2), p.225-230

2007

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Resource utilization and costs of transitioning from pediatric to adult care for patients with chronic autoinflammatory and autoimmune disorders

Pediatric rheumatology online journal, 2024-02, Vol.22 (1), p.28-28, Article 28

2024

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A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Document

European journal of human genetics : EJHG, 2014-01, Vol.22 (1), p.12-17

2014

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Determinants of Plasma Docosahexaenoic Acid Levels and Their Relationship to Neurological and Cognitive Functions in PKU Patients: A Double Blind Randomized Supplementation Study

Nutrients, 2018-12, Vol.10 (12), p.1944

2018

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William L. Nyhan, Georg F. Hoffmann. Atlas of inherited metabolic diseases (Hardcover and e-Book) 4th ed. Boca Raton: CRC Press, Taylor & Francis Group, 2020, 855 p., $175; £120, €124. ISBN-13: 9781138196599. (With contributions from Aida I. Al-Aqeel and Bruce A. Barshop)

Journal of inherited metabolic disease, 2020-12

Burgard, Peter

2020

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A holistic approach to the patients/Families with inborn errors of metabolism

Journal of Mother and Child, 2020-10, Vol.24 (2), p.65-72

Burgard, Peter

2020

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Differences of Phenylalanine Concentrations in Dried Blood Spots and in Plasma: Erythrocytes as a Neglected Component for This Observation

Metabolites, 2021-10, Vol.11 (10), p.680

2021

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On being an editor, reviewer, and author—different sides of the same coin

Journal of inherited metabolic disease, 2019-01, Vol.42 (1), p.1-2

2019

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Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I — A decade of experience

Molecular genetics and metabolism, 2012-09, Vol.107 (1-2), p.72-80

2012

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A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype

American journal of human genetics, 1998-07, Vol.63 (1), p.71-79

1998

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Strukturierte Aufklärung und Beratung bei monogen vererbten Stoffwechselkrankheiten

Medizinische Genetik, 2015-10, Vol.27 (3), p.296-301

2015

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Ein strukturierter Versorgungspfad von der Pädiatrie in die Erwachsenenmedizin für Jugendliche und junge Erwachsene mit einer seltenen Erkrankung: Modell und Praxis im Innovationsfonds Projekt TRANSLATE-NAMSE

Monatsschrift Kinderheilkunde, 2022, Vol.170 (1), p.61-69

2022

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Allelic phenotype values: a model for genotype-based phenotype prediction in phenylketonuria

Genetics in medicine, 2019-03, Vol.21 (3), p.580-590

2019

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Der klinische Versorgungspfad zur multiprofessionellen Versorgung seltener Erkrankungen in der Pädiatrie – Ergebnisse aus dem Projekt TRANSLATE-NAMSE

Monatsschrift Kinderheilkunde, 2022, Vol.170 (1), p.52-60

2022

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Resource use and costs of transitioning from paediatric to adult care for patients with chronic endocrine disease

Clinical endocrinology (Oxford), 2024-08, Vol.101 (2), p.121-129

2024

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Das Verhaeltnis von Moral und Recht in entwicklungspsychologischen Strukturtheorien des moralischen Urteils: E. piagetian. Analyse

Burgard, Peter

1986

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Baroque: Figures of Excess in Seventeenth-Century European Art and German Literature

Impact of glycogen storage disease type I on adult daily life: a survey

Efficacy and outcome of expanded newborn screening for metabolic diseases--report of 10 years from South-West Germany

Impact of Diagnosis and Therapy on Cognitive Function in Urea Cycle Disorders

William L. Nyhan, Georg F. Hoffmann. Atlas of inherited metabolic diseases (Hardcover and e‐Book) 4th ed. Boca Raton: CRC Press, Taylor & Francis Group, 2020, 855 p., $175; £120, €124. ISBN‐13: 9781138196599. (With contributions from Aida I. Al‐Aqeel and Bruce A. Barshop)

An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Federal Joint Committee

Transition for adolescents with a rare disease: results of a nationwide German project

High blood pressure, a red flag for the neonatal manifestation of urea cycle disorders

Long-term outcome in methylmalonic acidurias is influenced by the underlying defect (mut0, mut- , cblA, cblB)

Resource utilization and costs of transitioning from pediatric to adult care for patients with chronic autoinflammatory and autoimmune disorders

ASL Metabolically Regulates Tyrosine Hydroxylase in the Nucleus Locus Coeruleus

A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Document

Determinants of Plasma Docosahexaenoic Acid Levels and Their Relationship to Neurological and Cognitive Functions in PKU Patients: A Double Blind Randomized Supplementation Study

William L. Nyhan, Georg F. Hoffmann. Atlas of inherited metabolic diseases (Hardcover and e-Book) 4th ed. Boca Raton: CRC Press, Taylor & Francis Group, 2020, 855 p., $175; £120, €124. ISBN-13: 9781138196599. (With contributions from Aida I. Al-Aqeel and Bruce A. Barshop)

A holistic approach to the patients/Families with inborn errors of metabolism

Differences of Phenylalanine Concentrations in Dried Blood Spots and in Plasma: Erythrocytes as a Neglected Component for This Observation

On being an editor, reviewer, and author—different sides of the same coin

Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I — A decade of experience

A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype

Strukturierte Aufklärung und Beratung bei monogen vererbten Stoffwechselkrankheiten

Ein strukturierter Versorgungspfad von der Pädiatrie in die Erwachsenenmedizin für Jugendliche und junge Erwachsene mit einer seltenen Erkrankung: Modell und Praxis im Innovationsfonds Projekt TRANSLATE-NAMSE

Allelic phenotype values: a model for genotype-based phenotype prediction in phenylketonuria

Der klinische Versorgungspfad zur multiprofessionellen Versorgung seltener Erkrankungen in der Pädiatrie – Ergebnisse aus dem Projekt TRANSLATE-NAMSE

Resource use and costs of transitioning from paediatric to adult care for patients with chronic endocrine disease

Das Verhaeltnis von Moral und Recht in entwicklungspsychologischen Strukturtheorien des moralischen Urteils: E. piagetian. Analyse

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