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Lambert P W J van den Heuvel

Showing results (1-10 of 24) with videos related to

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Pediatric Nephrology (Berlin, Germany)|March 31, 2006
Teaching molecular genetics: Chapter 3--Proteomics in nephrologyPatricia J T A Groenen, Lambert P W J van den Heuvel
The Lancet. Neurology|July 25, 2003
Heparan sulphate proteoglycans in Alzheimer's disease and amyloid-related disordersJack van Horssen, Pieter Wesseling, Lambert P W J van den Heuvel, et al.
Journal of Nephrology|May 28, 2003
Genetic renal disorders with hypomagnesemia and hypocalciuriaNine V A M Knoers, Joke C de Jong, Iwan C Meij, et al.
Journal of Inherited Metabolic Disease|March 10, 2012
Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A > G mutationPaul de Laat, Saskia Koene, Lambert P W J van den Heuvel, et al.
Pediatric Nephrology (Berlin, Germany)|September 25, 2012
The challenge of managing hemophilia A and STEC-induced hemolytic uremic syndromeDineke Westra, Eiske M Dorresteijn, Auke Beishuizen, et al.
Journal of Human Genetics|February 1, 2003
A novel splice site mutation in neonatal carnitine palmitoyl transferase II deficiencyRoel J P Smeets, Jan A M Smeitink, Ben A Semmekrot, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 31, 2022
Kidney injury rates after unilateral nephrectomy in childhood-a systematic review and meta-analysisSander Groen In 't Woud, Alessandro Gobino, Nel Roeleveld, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 14, 2003
Exclusion of mutations in FXYD2, CLDN16 and SLC12A3 in two families with primary renal Mg2+ lossIwan C Meij, Lambert P W J van den Heuvel, Sies Hemmes, et al.
Molecular Genetics and Metabolism|March 27, 2007
Investigation of the complex I assembly chaperones B17.2L and NDUFAF1 in a cohort of CI deficient patientsRutger O Vogel, Mariël A M van den Brand, Richard J Rodenburg, et al.
The Journal of Biological Chemistry|January 9, 2007
Identification of mitochondrial complex I assembly intermediates by tracing tagged NDUFS3 demonstrates the entry point of mitochondrial subunitsRutger O Vogel, Cindy E J Dieteren, Lambert P W J van den Heuvel, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Pediatric Nephrology (Berlin, Germany)|March 31, 2006
Teaching molecular genetics: Chapter 3--Proteomics in nephrologyPatricia J T A Groenen, Lambert P W J van den Heuvel
The Lancet. Neurology|July 25, 2003
Heparan sulphate proteoglycans in Alzheimer's disease and amyloid-related disordersJack van Horssen, Pieter Wesseling, Lambert P W J van den Heuvel, et al.
Journal of Nephrology|May 28, 2003
Genetic renal disorders with hypomagnesemia and hypocalciuriaNine V A M Knoers, Joke C de Jong, Iwan C Meij, et al.
Journal of Inherited Metabolic Disease|March 10, 2012
Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A > G mutationPaul de Laat, Saskia Koene, Lambert P W J van den Heuvel, et al.
Pediatric Nephrology (Berlin, Germany)|September 25, 2012
The challenge of managing hemophilia A and STEC-induced hemolytic uremic syndromeDineke Westra, Eiske M Dorresteijn, Auke Beishuizen, et al.
Journal of Human Genetics|February 1, 2003
A novel splice site mutation in neonatal carnitine palmitoyl transferase II deficiencyRoel J P Smeets, Jan A M Smeitink, Ben A Semmekrot, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 31, 2022
Kidney injury rates after unilateral nephrectomy in childhood-a systematic review and meta-analysisSander Groen In 't Woud, Alessandro Gobino, Nel Roeleveld, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 14, 2003
Exclusion of mutations in FXYD2, CLDN16 and SLC12A3 in two families with primary renal Mg2+ lossIwan C Meij, Lambert P W J van den Heuvel, Sies Hemmes, et al.
Molecular Genetics and Metabolism|March 27, 2007
Investigation of the complex I assembly chaperones B17.2L and NDUFAF1 in a cohort of CI deficient patientsRutger O Vogel, Mariël A M van den Brand, Richard J Rodenburg, et al.
The Journal of Biological Chemistry|January 9, 2007
Identification of mitochondrial complex I assembly intermediates by tracing tagged NDUFS3 demonstrates the entry point of mitochondrial subunitsRutger O Vogel, Cindy E J Dieteren, Lambert P W J van den Heuvel, et al.
Pageof 3