Suchergebnisse - "Rittig, Søren"

PubPharm (11)

1

Acute intravenous acyl ghrelin infusion induces thirst but does not affect sodium excretion : two randomized, double-blind, placebo-controlled crossover studies in hypopituitary patients

enthalten in: European journal of endocrinology | 2019

von Vestergaard, E. | Møller, N. | Andersen, R. | +2

2

Induced pluripotent stem cells derived from a patient with autosomal dominant familial neurohypophyseal diabetes insipidus caused by a variant in the AVP gene

enthalten in: Stem cell research | 2017

von Toustrup, L. | Zhou, Y. | Kvistgaard, H. | +6

3

Nephrogenic diabetes insipidus : essential insights into the molecular background and potential therapies for treatment

enthalten in: Endocrine reviews | 2013

von Moeller, H. | Rittig, S. | Fenton, R.

4

Late-onset familial neurohypophyseal diabetes insipidus due to a novel mutation in the AVP gene

enthalten in: Clinical endocrinology | 2012

von Jendle, J. | Christensen, J. | Kvistgaard, H. | +2

5

Excess diuresis and natriuresis during acute sleep deprivation in healthy adults

enthalten in: American journal of physiology. Renal physiology | 2010

von Kamperis, K. | Hagstroem, S. | Radvanska, E. | +2

6

Expression of three different mutations in the arginine vasopressin gene suggests genotype-phenotype correlation in familial neurohypophyseal diabetes insipidus kindreds

enthalten in: Clinical endocrinology | 2005

von Siggaard, C. | Christensen, J. | Corydon, T. | +5

7

Differential cellular handling of defective arginine vasopressin (AVP) prohormones in cells expressing mutations of the AVP gene associated with autosomal dominant and recessive familial neurohypophyseal diabetes insipidus

enthalten in: The Journal of clinical endocrinology and metabolism | 2004

von Christensen, J. | Siggaard, C. | Corydon, T. | +4

8

Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis

enthalten in: European journal of human genetics : EJHG | 2004

von Christensen, J. | Siggaard, C. | Corydon, T. | +5

9

Impaired trafficking of mutated AVP prohormone in cells expressing rare disease genes causing autosomal dominant familial neurohypophyseal diabetes insipidus

enthalten in: Clinical endocrinology | 2004

von Christensen, J. | Siggaard, C. | Corydon, T. | +4

10

Autosomal dominant familial neurohypophyseal diabetes insipidus

enthalten in: APMIS. Supplementum | 2003

von Christensen, J. | Siggaard, C. | Rittig, S.