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L P van den Heuvel

Showing results (1-10 of 153) with videos related to

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Human Genetics|November 19, 2002
Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2)L P van den Heuvel, K Assink, M Willemsen, et al.
Advances in Nephrology From the Necker Hospital|November 9, 2000
Inherited hypomagnesemiaI C Meij, L P van den Heuvel, N V Knoers
Current Opinion in Neurology|November 28, 2001
Mitochondrial oxidative phosphorylation system assembly in man: recent achievementsM J Coenen, L P van den Heuvel, J A Smeitink
Health Policy (Amsterdam, Netherlands)|November 3, 1997
Utilisation of medical technology assessment in health policyW J van den Heuvel, R Wieringh, L P van den Heuvel
Mitochondrion|August 27, 2005
Biochemical examination of fibroblasts in the diagnosis and research of oxidative phosphorylation (OXPHOS) defectsL P van den Heuvel, J A Smeitink, R J T Rodenburg
Annals of Clinical Biochemistry|January 25, 2003
Some practical aspects of providing a diagnostic service for respiratory chain defectsA J M Janssen, J A M Smeitink, L P van den Heuvel
Nederlands Tijdschrift Voor Geneeskunde|December 26, 2003
[From gene to disease; congenital thrombotic thrombocytopenic purpura due to mutations in the ADAMTS13 gene]R H Schiphorst, N C van de Kar, L P van den Heuvel
Journal of Inherited Metabolic Disease|October 19, 2013
Sequence variants in four candidate genes (NIPSNAP1, GBAS, CHCHD1 and METT11D1) in patients with combined oxidative phosphorylation system deficienciesP Smits, R J Rodenburg, J A M Smeitink, et al.
The International Journal of Biochemistry|January 1, 1988
Heparan sulfate proteoglycan from human and equine glomeruli and tubulesL P van den Heuvel, J H Veerkamp, L A Monnens, et al.
American Journal of Medical Genetics|October 2, 2001
Respiratory chain complex I deficiencyR H Triepels, L P Van Den Heuvel, J M Trijbels, et al.
Pageof 16

Showing results (1-10 of 153) with videos related to

Sort By:
Pageof 16
Human Genetics|November 19, 2002
Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2)L P van den Heuvel, K Assink, M Willemsen, et al.
Advances in Nephrology From the Necker Hospital|November 9, 2000
Inherited hypomagnesemiaI C Meij, L P van den Heuvel, N V Knoers
Current Opinion in Neurology|November 28, 2001
Mitochondrial oxidative phosphorylation system assembly in man: recent achievementsM J Coenen, L P van den Heuvel, J A Smeitink
Health Policy (Amsterdam, Netherlands)|November 3, 1997
Utilisation of medical technology assessment in health policyW J van den Heuvel, R Wieringh, L P van den Heuvel
Mitochondrion|August 27, 2005
Biochemical examination of fibroblasts in the diagnosis and research of oxidative phosphorylation (OXPHOS) defectsL P van den Heuvel, J A Smeitink, R J T Rodenburg
Annals of Clinical Biochemistry|January 25, 2003
Some practical aspects of providing a diagnostic service for respiratory chain defectsA J M Janssen, J A M Smeitink, L P van den Heuvel
Nederlands Tijdschrift Voor Geneeskunde|December 26, 2003
[From gene to disease; congenital thrombotic thrombocytopenic purpura due to mutations in the ADAMTS13 gene]R H Schiphorst, N C van de Kar, L P van den Heuvel
Journal of Inherited Metabolic Disease|October 19, 2013
Sequence variants in four candidate genes (NIPSNAP1, GBAS, CHCHD1 and METT11D1) in patients with combined oxidative phosphorylation system deficienciesP Smits, R J Rodenburg, J A M Smeitink, et al.
The International Journal of Biochemistry|January 1, 1988
Heparan sulfate proteoglycan from human and equine glomeruli and tubulesL P van den Heuvel, J H Veerkamp, L A Monnens, et al.
American Journal of Medical Genetics|October 2, 2001
Respiratory chain complex I deficiencyR H Triepels, L P Van Den Heuvel, J M Trijbels, et al.
Pageof 16