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Researcher
id
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First name
Bibiche
Prefix
den
Last name
Hollander
Name
Bibiche den Hollander
Blocked
Main program
Metabolism
Short description of the research
Research on new treatment strategies for rare hereditary metabolic diseases, with a focus on the application of personalized medicine and N-of-1 study designs. I have worked on establishing an infrastructure for conducting investigator-initiated clinical studies to generate evidence for (emerging) therapies for these rare conditions.
Diseases
Inborn errors of metabolism
Gaucher disease
Mucopolysaccharidosis type 3a (Sanfilippo syndrome)
GRIN2B-neurodevelopmental disorder
NANS-CDG
Lipoprotein lipase deficiency
Diseases
Inborn errors of metabolism
Other diseases
Research topics
Clinical outcomes
Drug metabolism
Lipid metabolism
Metabolomics
Pharmacology
Quality of life
Research topics
Clinical outcomes
Drug metabolism
Lipid metabolism
Metabolomics
Pharmacology
Quality of life
Other topics
Cells/tissues
Brain
Pancreas
Plasma
Cells/tissues
Brain
Pancreas
Plasma
Other cells/tissues
Research techniques
Clinical trials/intervention studies
Metabolomics
Observational/epidemiology studies
Research techniques
Clinical trials/intervention studies
Metabolomics
Observational/epidemiology studies
Other techniques
Department
Pediatric Metabolic Diseases
Location/affiliation
AMC
UvA
United for Metebolic Disease
Location/affiliation
AMC
UvA
Other location
Function
PhD candidate
PI
E-mail address
Link to personal website or LinkedIn
https://www.linkedin.com/in/bibiche-den-hollander-b233241aa/
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