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A M Bosch

Showing results (31-40 of 46) with videos related to

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The British Journal of Dermatology|October 10, 1998
Iatrogenic isolated isoleucine deficiency as the cause of an acrodermatitis enteropathica-like syndromeA M Bosch, J H Sillevis Smitt, A H Van Gennip, et al.
Journal of Inherited Metabolic Disease|August 31, 2023
Food or medicine? A European regulatory perspective on nutritional therapy products to treat inborn errors of metabolismN N Stolwijk, A M Bosch, N Bouwhuis, et al.
JIMD Reports|May 22, 2016
Establishing New Cut-Off Limits for Galactose 1-Phosphate-Uridyltransferase Deficiency for the Dutch Newborn Screening ProgrammeE A Kemper, A Boelen, A M Bosch, et al.
Journal of Inherited Metabolic Disease|September 19, 2007
High incidence of hypermethioninaemia in a single neonatal intensive care unit detected by a newly introduced neonatal screening programmeA E ten Hoedt, A A van Kempen, A Boelen, et al.
The British Journal of Radiology|May 24, 2003
Interexamination variation of whole breast ultrasoundA M Bosch, A G H Kessels, G L Beets, et al.
Journal of Inherited Metabolic Disease|January 9, 2009
Phenylalanine tolerance can already reliably be assessed at the age of 2 years in patients with PKUF J van Spronsen, M van Rijn, B Dorgelo, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
The intake of total protein, natural protein and protein substitute and growth of height and head circumference in Dutch infants with phenylketonuriaM Hoeksma, M Van Rijn, P H Verkerk, 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.
Psychological Medicine|May 30, 2017
Cerebral dopamine deficiency, plasma monoamine alterations and neurocognitive deficits in adults with phenylketonuriaE Boot, C E M Hollak, S C J Huijbregts, 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.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
The British Journal of Dermatology|October 10, 1998
Iatrogenic isolated isoleucine deficiency as the cause of an acrodermatitis enteropathica-like syndromeA M Bosch, J H Sillevis Smitt, A H Van Gennip, et al.
Journal of Inherited Metabolic Disease|August 31, 2023
Food or medicine? A European regulatory perspective on nutritional therapy products to treat inborn errors of metabolismN N Stolwijk, A M Bosch, N Bouwhuis, et al.
JIMD Reports|May 22, 2016
Establishing New Cut-Off Limits for Galactose 1-Phosphate-Uridyltransferase Deficiency for the Dutch Newborn Screening ProgrammeE A Kemper, A Boelen, A M Bosch, et al.
Journal of Inherited Metabolic Disease|September 19, 2007
High incidence of hypermethioninaemia in a single neonatal intensive care unit detected by a newly introduced neonatal screening programmeA E ten Hoedt, A A van Kempen, A Boelen, et al.
The British Journal of Radiology|May 24, 2003
Interexamination variation of whole breast ultrasoundA M Bosch, A G H Kessels, G L Beets, et al.
Journal of Inherited Metabolic Disease|January 9, 2009
Phenylalanine tolerance can already reliably be assessed at the age of 2 years in patients with PKUF J van Spronsen, M van Rijn, B Dorgelo, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
The intake of total protein, natural protein and protein substitute and growth of height and head circumference in Dutch infants with phenylketonuriaM Hoeksma, M Van Rijn, P H Verkerk, 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.
Psychological Medicine|May 30, 2017
Cerebral dopamine deficiency, plasma monoamine alterations and neurocognitive deficits in adults with phenylketonuriaE Boot, C E M Hollak, S C J Huijbregts, 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.
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