Lambertus P. van den Heuvel
Rega Institute for Medical Research(BE)University Medical Center(US)
Publications by Year
Research Areas
Complement system in diseases, Biomedical Research and Pathophysiology, Renal Diseases and Glomerulopathies, Neonatal Health and Biochemistry, Mitochondrial Function and Pathology
Most-Cited Works
- → Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida(1995)871 cited
- Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease.(1996)
- → Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia(2007)359 cited
- → Mitochondrial complex I deficiency: from organelle dysfunction to clinical disease(2008)313 cited
- → Isolated complex I deficiency in children: Clinical, biochemical and genetic aspects(2000)289 cited
- → Mutations in the Chloride Channel Gene CLCNKB as a Cause of Classic Bartter Syndrome(2000)288 cited
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