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Journal of Neurosurgery. Spine
|
April 18, 2007
Cervical high-intensity intramedullary lesions without spinal cord compression in achondroplasia
J Marc C van Dijk, Charlotte M A Lubout, Patrick A Brouwer
Nutrients
|
October 14, 2022
Communication of an Abnormal Metabolic New-Born Screening Result in The Netherlands: The Parental Perspective
Sietske Haitjema, Charlotte M A Lubout, Justine H M Zijlstra, et al.
International Journal of Neonatal Screening
|
August 22, 2025
Communication of an Abnormal Metabolic Newborn Screening Result in the Netherlands: A Qualitative Exploratory Study of the General Practitioner's Perspective
Sietske Haitjema, Charlotte M A Lubout, Justine H M Zijlstra, et al.
Clinical Genetics
|
July 6, 2022
Expanding the clinical spectrum of primary coenzyme Q10 deficiency type 6: The first case with cardiomyopathy
Lisette Leeuwen, Charlotte M A Lubout, Hessel P Nijenhuis, et al.
Nutrition (Burbank, Los Angeles County, Calif.)
|
June 22, 2026
Living with phenylketonuria in adulthood
Sietske Haitjema, Jade S Timmenga, Charlotte M A Lubout, et al.
Nutrition (Burbank, Los Angeles County, Calif.)
|
March 6, 2022
Dietary treatment in Dutch children with phenylketonuria: An inventory of associated social restrictions and eating problems
Sietske Haitjema, Charlotte M A Lubout, David Abeln, et al.
Molecular Genetics and Metabolism
|
September 7, 2024
Continuous glucose monitoring metrics in people with liver glycogen storage disease and idiopathic ketotic hypoglycemia: A single-center, retrospective, observational study
Ruben J Overduin, Annieke Venema, Charlotte M A Lubout, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 25, 2017
Molybdenum cofactor deficiency type A: Prenatal monitoring using MRI
Charlotte M A Lubout, Terry G J Derks, Linda Meiners, et al.
Pediatric Neurology
|
August 3, 2019
Successful Treatment of Hereditary Folate Malabsorption With Intramuscular Folinic Acid
Charlotte M A Lubout, Susanna M I Goorden, Karin van den Hurk, et al.
Journal of Inherited Metabolic Disease
|
September 11, 2019
The first European guidelines on phenylketonuria: Usefulness and implications for BH<sub>4</sub> responsiveness testing
Roeland A F Evers, Annemiek M J van Wegberg, Karen Anjema, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 23) with videos related to
Sort By:
Page
of 3
Journal of Neurosurgery. Spine
|
April 18, 2007
Cervical high-intensity intramedullary lesions without spinal cord compression in achondroplasia
J Marc C van Dijk, Charlotte M A Lubout, Patrick A Brouwer
Nutrients
|
October 14, 2022
Communication of an Abnormal Metabolic New-Born Screening Result in The Netherlands: The Parental Perspective
Sietske Haitjema, Charlotte M A Lubout, Justine H M Zijlstra, et al.
International Journal of Neonatal Screening
|
August 22, 2025
Communication of an Abnormal Metabolic Newborn Screening Result in the Netherlands: A Qualitative Exploratory Study of the General Practitioner's Perspective
Sietske Haitjema, Charlotte M A Lubout, Justine H M Zijlstra, et al.
Clinical Genetics
|
July 6, 2022
Expanding the clinical spectrum of primary coenzyme Q10 deficiency type 6: The first case with cardiomyopathy
Lisette Leeuwen, Charlotte M A Lubout, Hessel P Nijenhuis, et al.
Nutrition (Burbank, Los Angeles County, Calif.)
|
June 22, 2026
Living with phenylketonuria in adulthood
Sietske Haitjema, Jade S Timmenga, Charlotte M A Lubout, et al.
Nutrition (Burbank, Los Angeles County, Calif.)
|
March 6, 2022
Dietary treatment in Dutch children with phenylketonuria: An inventory of associated social restrictions and eating problems
Sietske Haitjema, Charlotte M A Lubout, David Abeln, et al.
Molecular Genetics and Metabolism
|
September 7, 2024
Continuous glucose monitoring metrics in people with liver glycogen storage disease and idiopathic ketotic hypoglycemia: A single-center, retrospective, observational study
Ruben J Overduin, Annieke Venema, Charlotte M A Lubout, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 25, 2017
Molybdenum cofactor deficiency type A: Prenatal monitoring using MRI
Charlotte M A Lubout, Terry G J Derks, Linda Meiners, et al.
Pediatric Neurology
|
August 3, 2019
Successful Treatment of Hereditary Folate Malabsorption With Intramuscular Folinic Acid
Charlotte M A Lubout, Susanna M I Goorden, Karin van den Hurk, et al.
Journal of Inherited Metabolic Disease
|
September 11, 2019
The first European guidelines on phenylketonuria: Usefulness and implications for BH<sub>4</sub> responsiveness testing
Roeland A F Evers, Annemiek M J van Wegberg, Karen Anjema, et al.
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of 3