Rees, David C.

Sickle-cell disease

Rees, D. C., Williams, T. N., & Gladwin, M. T. (2010) · The Lancet

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 2,504

Sickle cell disease

Piel, F. B., Steinberg, M. H., & Rees, D. C. (2017) · New England Journal of Medicine

Hemoglobinopathies and Related DisordersMalaria Research and Control

Cited by 1,488

Phase 3 Trial of RNAi Therapeutic Givosiran for Acute Intermittent Porphyria

Balwani, M., Sardh, E., Ventura, P., Peiró, P. A., Rees, D. C., Stölzel, U., Bissell, D. M., Bonkovsky, H. L., Windyga, J., Anderson, K. E., et al. (2020) · New England Journal of Medicine

Porphyrin Metabolism and DisordersNeonatal Health and Biochemistry

Cited by 608

Acute haemolysis induced by high dose ascorbic acid in glucose-6-phosphate dehydrogenase deficiency.

Rees, D. C., Kelsey, H., & Richards, J. D. (1993) · BMJ

Neonatal Health and BiochemistryMethemoglobinemia and Tumor Lysis Syndrome

Cited by 191

g(HbF): a genetic model of fetal hemoglobin in sickle cell disease

Gardner, K., Fulford, T., Silver, N., Rooks, H., Angelis, N., Allman, M., Nkya, S., Makani, J., Howard, J., Kesse-Adu, R., et al. (2018) · Blood Advances

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 43