Rösler, Ariel

Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1

Chang, S. S., Grunder, S., Hanukoglu, A., Rösler, A., Mathew, P. M., Hanukoglu, I., Schild, L., Lu, Y., Shimkets, R. A., Nelson-Williams, C., et al. (1996) · Nature Genetics

Ion Transport and Channel RegulationIon channel regulation and function

Cited by 808

A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin.

White, P. C., Dupont, J., New, M. I., Leiberman, E., Hochberg, Z., & Rösler, A. (1991) · Journal of Clinical Investigation

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 267

Treatment of men with paraphilia with a long-acting analogue of gonadotropin-releasing hormone

Rösler, A., & Witztum, E. (1998) · New England Journal of Medicine

Psychopathy, Forensic Psychiatry, Sexual OffendingSexuality, Behavior, and Technology

Cited by 217

Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency.

Pascoe, L., Curnow, K. M., Slutsker, L., Rösler, A., & White, P. C. (1992) · Proceedings of the National Academy of Sciences

Hormonal Regulation and HypertensionAdrenal Hormones and Disorders

Cited by 188

The natural history of salt-wasting disorders of adrenal and renal origin

RÖSLER, A. (1984) · The Journal of Clinical Endocrinology & Metabolism

Hormonal Regulation and HypertensionAdrenal Hormones and Disorders

Cited by 125