Browse by Basel Contributors ID

2020

Spiess, Martin and Beuret, Nicole and Rutishauser, Jonas. (2020) Genetic forms of neurohypophyseal diabetes insipidus. Best Practice and Research Clinical Endocrinology and Metabolism, 34 (5). p. 101432.

Spiess, Martin and Beuret, Nicole and Prescianotto Baschong, Cristina and Rutishauser, Jonas. (2020) Amyloid-like aggregation of provasopressin. Vitamins and hormones, 113. pp. 55-77.

Spiess, Martin and Friberg, Michael and Beuret, Nicole and Prescianotto-Baschong, Cristina and Rutishauser, Jonas. (2020) Role of protein aggregation and degradation in autosomal dominant neurohypophyseal diabetes insipidus. Molecular and cellular endocrinology, 501. p. 110653.

2013

Seuring, C. and Nespovitaya, N. and Rutishauser, J. and Spiess, M. and Riek, R.. (2013) Hormone amyloids in sickness and in health. In: Amyloid fibrils and prefibrillar aggregates : molecular and biological properties. Weinheim, Germany, pp. 395-410.

2011

Balanescu, Sandrina and Kopp, Peter and Gaskill, Mary Beth and Morgenthaler, Nils G. and Schindler, Christian and Rutishauser, Jonas. (2011) Correlation of plasma copeptin and vasopressin concentrations in hypo-, iso-, and hyperosmolar states. Journal of clinical endocrinology and metabolism, Vol. 96, H. 4. pp. 1046-1052.

Rutishauser, Jonas. (2011) Statins in clinical medicine. Swiss Medical Weekly, Vol. 141 , w13310.

Scheuter, Claudia and Rutishauser, Jonas. (2011) Hyponatriämie. Therapeutische Umschau, Vol. 68, H. 6. pp. 327-336.

Brachet, Cécile and Birk, Julia and Christophe, Catherine and Tenoutasse, Sylvie and Velkeniers, Brigitte and Heinrichs, Claudine and Rutishauser, Jonas. (2011) Growth retardation in untreated autosomal dominant familial neurohypophyseal diabetes insipidus caused by one recurring and two novel mutations in the vasopressin-neurophysin II gene. European journal of endocrinology, Vol. 164, H. 2. pp. 179-187.