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1. Behavioural and emotional problems, intellectual impairment and health‐related quality of life in patients with organic acidurias and urea cycle disorders. Issue 2 (27th August 2015)

2. Cystathionine β‐synthase deficiency in the E‐HOD registry‐part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis. Issue 3 (28th December 2020)

4. Early prediction of phenotypic severity in Citrullinemia Type 1. Issue 9 (30th August 2019)

5. Early prediction of phenotypic severity in Citrullinemia Type 1. Issue 9 (30th August 2019)

6. Erratum to: The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation. Issue 6 (16th June 2015)

7. Erratum to: The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype. Issue 6 (16th June 2015)

8. Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea‐cycle disorders: On the basis of information from a European multicenter registry. Issue 6 (27th February 2019)

9. From genotype to phenotype: Early prediction of disease severity in argininosuccinic aciduria. Issue 5 (30th January 2020)

10. Health‐related quality of life in paediatric patients with intoxication‐type inborn errors of metabolism: Analysis of an international data set. Issue 1 (22nd September 2020)