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Showing results (71-80 of 79) with videos related to

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Journal of Inherited Metabolic Disease|March 13, 2026
Long-Term Follow-Up of Patients With Transaldolase DeficiencyM Scaglione, A Brassier, A Wiedemann, et al.
Orphanet Journal of Rare Diseases|July 2, 2020
PKU dietary handbook to accompany PKU guidelinesA MacDonald, A M J van Wegberg, K Ahring, et al.
Orphanet Journal of Rare Diseases|September 3, 2020
Correction to: PKU dietary handbook to accompany PKU guidelinesA MacDonald, A M J van Wegberg, K Ahring, et al.
Orphanet Journal of Rare Diseases|October 14, 2017
The complete European guidelines on phenylketonuria: diagnosis and treatmentA M J van Wegberg, A MacDonald, K Ahring, et al.
Molecular Genetics and Metabolism|May 16, 2025
European guidelines on diagnosis and treatment of phenylketonuria: First revisionA M J van Wegberg, A MacDonald, K Ahring, et al.
Molecular Genetics and Metabolism|February 21, 2021
Defining tetrahydrobiopterin responsiveness in phenylketonuria: Survey results from 38 countriesR A F Evers, A M J van Wegberg, K Ahring, et al.
Molecular Genetics and Metabolism|October 27, 2015
The challenges of managing coexistent disorders with phenylketonuria: 30 casesA MacDonald, K Ahring, M F Almeida, et al.
Molecular Genetics and Metabolism Reports|March 10, 2017
Dietary practices in isovaleric acidemia: A European surveyA Pinto, A Daly, S Evans, et al.
Molecular Genetics and Metabolism Reports|October 13, 2017
Dietary practices in propionic acidemia: A European surveyA Daly, A Pinto, S Evans, et al.
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Showing results (71-80 of 79) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 79 results.
Journal of Inherited Metabolic Disease|March 13, 2026
Long-Term Follow-Up of Patients With Transaldolase DeficiencyM Scaglione, A Brassier, A Wiedemann, et al.
Orphanet Journal of Rare Diseases|July 2, 2020
PKU dietary handbook to accompany PKU guidelinesA MacDonald, A M J van Wegberg, K Ahring, et al.
Orphanet Journal of Rare Diseases|September 3, 2020
Correction to: PKU dietary handbook to accompany PKU guidelinesA MacDonald, A M J van Wegberg, K Ahring, et al.
Orphanet Journal of Rare Diseases|October 14, 2017
The complete European guidelines on phenylketonuria: diagnosis and treatmentA M J van Wegberg, A MacDonald, K Ahring, et al.
Molecular Genetics and Metabolism|May 16, 2025
European guidelines on diagnosis and treatment of phenylketonuria: First revisionA M J van Wegberg, A MacDonald, K Ahring, et al.
Molecular Genetics and Metabolism|February 21, 2021
Defining tetrahydrobiopterin responsiveness in phenylketonuria: Survey results from 38 countriesR A F Evers, A M J van Wegberg, K Ahring, et al.
Molecular Genetics and Metabolism|October 27, 2015
The challenges of managing coexistent disorders with phenylketonuria: 30 casesA MacDonald, K Ahring, M F Almeida, et al.
Molecular Genetics and Metabolism Reports|March 10, 2017
Dietary practices in isovaleric acidemia: A European surveyA Pinto, A Daly, S Evans, et al.
Molecular Genetics and Metabolism Reports|October 13, 2017
Dietary practices in propionic acidemia: A European surveyA Daly, A Pinto, S Evans, et al.
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