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Annet M Bosch

Showing results (51-60 of 103) with videos related to

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Clinical Biochemistry|March 6, 2023
Machine learning to improve false-positive results in the Dutch newborn screening for congenital hypothyroidismKevin Stroek, Allerdien Visser, Catharina P B van der Ploeg, et al.
Orphanet Journal of Rare Diseases|June 29, 2011
"MY PKU": increasing self-management in patients with phenylketonuria. A randomized controlled trialAmber E Ten Hoedt, Carla Em Hollak, Carolien Ca Boelen, et al.
Molecular Genetics and Metabolism|November 17, 2020
Gray and white matter are both affected in classical galactosemia: An explorative study on the association between neuroimaging and clinical outcomeMendy M Welsink-Karssies, Anouk Schrantee, Matthan W A Caan, et al.
Annals of Nutrition & Metabolism|January 18, 2018
Response to the Letter to the Editor Regarding "Micronutrients, Essential Fatty Acids and Bone Health in Phenylketonuria"Serwet Demirdas, Francjan J van Spronsen, Carla E M Hollak, et al.
Annals of Nutrition & Metabolism|March 24, 2017
Micronutrients, Essential Fatty Acids and Bone Health in PhenylketonuriaSerwet Demirdas, Francjan J van Spronsen, Carla E M Hollak, et al.
Journal of Inherited Metabolic Disease|December 15, 2010
High phenylalanine levels directly affect mood and sustained attention in adults with phenylketonuria: a randomised, double-blind, placebo-controlled, crossover trialAmber E ten Hoedt, Leo M J de Sonneville, Baudouin Francois, et al.
Metabolites|September 26, 2025
Reducing False Positives in Newborn Screening: The Role of Perinatal Factors in the Dutch NBS ProgramNils W F Meijer, Rose E Maase, Patricia L Hall, et al.
Journal of Inherited Metabolic Disease|November 27, 2010
Brown-Vialetto-Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatmentAnnet M Bosch, Nico G G M Abeling, Lodewijk Ijlst, et al.
Orphanet Journal of Rare Diseases|November 10, 2019
Reducing complexity: explaining inborn errors of metabolism and their treatment to children and adolescentsNina A Zeltner, Mendy M Welsink-Karssies, Markus A Landolt, et al.
Orphanet Journal of Rare Diseases|September 21, 2018
Fertility in classical galactosaemia, a study of N-glycan, hormonal and inflammatory gene interactionsHugh-Owen Colhoun, Estela M Rubio Gozalbo, Annet M Bosch, et al.
Pageof 11

Showing results (51-60 of 103) with videos related to

Sort By:
Pageof 11
Clinical Biochemistry|March 6, 2023
Machine learning to improve false-positive results in the Dutch newborn screening for congenital hypothyroidismKevin Stroek, Allerdien Visser, Catharina P B van der Ploeg, et al.
Orphanet Journal of Rare Diseases|June 29, 2011
"MY PKU": increasing self-management in patients with phenylketonuria. A randomized controlled trialAmber E Ten Hoedt, Carla Em Hollak, Carolien Ca Boelen, et al.
Molecular Genetics and Metabolism|November 17, 2020
Gray and white matter are both affected in classical galactosemia: An explorative study on the association between neuroimaging and clinical outcomeMendy M Welsink-Karssies, Anouk Schrantee, Matthan W A Caan, et al.
Annals of Nutrition & Metabolism|January 18, 2018
Response to the Letter to the Editor Regarding "Micronutrients, Essential Fatty Acids and Bone Health in Phenylketonuria"Serwet Demirdas, Francjan J van Spronsen, Carla E M Hollak, et al.
Annals of Nutrition & Metabolism|March 24, 2017
Micronutrients, Essential Fatty Acids and Bone Health in PhenylketonuriaSerwet Demirdas, Francjan J van Spronsen, Carla E M Hollak, et al.
Journal of Inherited Metabolic Disease|December 15, 2010
High phenylalanine levels directly affect mood and sustained attention in adults with phenylketonuria: a randomised, double-blind, placebo-controlled, crossover trialAmber E ten Hoedt, Leo M J de Sonneville, Baudouin Francois, et al.
Metabolites|September 26, 2025
Reducing False Positives in Newborn Screening: The Role of Perinatal Factors in the Dutch NBS ProgramNils W F Meijer, Rose E Maase, Patricia L Hall, et al.
Journal of Inherited Metabolic Disease|November 27, 2010
Brown-Vialetto-Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatmentAnnet M Bosch, Nico G G M Abeling, Lodewijk Ijlst, et al.
Orphanet Journal of Rare Diseases|November 10, 2019
Reducing complexity: explaining inborn errors of metabolism and their treatment to children and adolescentsNina A Zeltner, Mendy M Welsink-Karssies, Markus A Landolt, et al.
Orphanet Journal of Rare Diseases|September 21, 2018
Fertility in classical galactosaemia, a study of N-glycan, hormonal and inflammatory gene interactionsHugh-Owen Colhoun, Estela M Rubio Gozalbo, Annet M Bosch, et al.
Pageof 11