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Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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C Boelen

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Journal of Inherited Metabolic Disease|November 8, 2003

Exercise intolerance, muscle pain and lactic acidaemia associated with a 7497G>A mutation in the tRNASer(UCN) geneO Grafakou, F A Hol, K Otfried Schwab, et al.

Japan-Hospitals : the Journal of the Japan Hospital Association|January 6, 2001

Asking the world experts in family medicine. Suggestions for the Hokkaido Centre for Family MedicineR Kassai, C Boelen, J G Cauffman, et al.

Pediatric Research|May 1, 1996

Short-term efficacy and safety of pravastatin in 72 children with familial hypercholesterolemiaH C Knipscheer, C C Boelen, J J Kastelein, et al.

Journal of Inherited Metabolic Disease|February 10, 2004

Clinical heterogeneity in patients with mutations in the NDUFS4 gene of mitochondrial complex IS M S Budde, L P W J van den Heuvel, R J P Smeets, et al.

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Search research articles

Showing results (21-30 of 24) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 24 results.

Journal of Inherited Metabolic Disease|November 8, 2003

Exercise intolerance, muscle pain and lactic acidaemia associated with a 7497G>A mutation in the tRNASer(UCN) geneO Grafakou, F A Hol, K Otfried Schwab, et al.

Japan-Hospitals : the Journal of the Japan Hospital Association|January 6, 2001

Asking the world experts in family medicine. Suggestions for the Hokkaido Centre for Family MedicineR Kassai, C Boelen, J G Cauffman, et al.

Pediatric Research|May 1, 1996

Short-term efficacy and safety of pravastatin in 72 children with familial hypercholesterolemiaH C Knipscheer, C C Boelen, J J Kastelein, et al.

Journal of Inherited Metabolic Disease|February 10, 2004

Clinical heterogeneity in patients with mutations in the NDUFS4 gene of mitochondrial complex IS M S Budde, L P W J van den Heuvel, R J P Smeets, et al.

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