Rootwelt, Helge

Self-induced correction of the genetic defect in tyrosinemia type I.

Kvittingen, E. A., Rootwelt, H., Berger, R., & Brandtzaeg, P. (1994) · Journal of Clinical Investigation

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 168

Hereditary tyrosinemia type I: Self-induced correction of the fumarylacetoacetase defect

Kvittingen, E. A., Rootwelt, H., Brandtzaeg, P., Bergan, A., & Berger, R. (1993) · Journal of Clinical Investigation

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 102

Effects of APOE on brain white matter microstructure in healthy adults

Westlye, L. T., Reinvang, I., Rootwelt, H., & Espeseth, T. (2012) · Neurology

Advanced Neuroimaging Techniques and ApplicationsAlzheimer's disease research and treatments

Cited by 84

Apolipoprotein E ε4-related thickening of the cerebral cortex modulates selective attention

Espeseth, T., Westlye, L. T., Walhovd, K. B., Fjell, A. M., Endestad, T., Rootwelt, H., & Reinvang, I. (2012) · Neurobiology of Aging

Dementia and Cognitive Impairment ResearchNeural and Behavioral Psychology Studies

Cited by 32

Two missense mutations causing tyrosinemia type 1 with presence and absence of immunoreactive fumarylacetoacetase

Rootwelt, H., Chou, J., Gahl, W. A., Berger, R., Coşkun, T., Brodtkorb, E., & Kvittingen, E. A. (1994) · Human Genetics

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 23

Tyrosinemia type 1 ? complex splicing defects and a missense mutation in the fumarylacetoacetase gene

Rootwelt, H., Kristensen, T., Berger, R., H�ie, K., & Kvittingen, E. (1994) · Human Genetics

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 23

Hereditary Tyrosinemia Type I: Lack of Correlation between Clinical Findings and Amount of Immunoreactive Fumarylacetoacetase Protein

Kvittingen, E. A., Rootwelt, H., van Dam, T., van Faassen, H., & Berger, R. (1992) · Pediatric Research

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 21

APOE polymorphism is associated with changes in the kynurenine pathway

Farup, P. G., Rootwelt, H., & Hestad, K. (2023) · Genes

Tryptophan and brain disordersAdipokines, Inflammation, and Metabolic Diseases

Cited by 1