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European Journal of Endocrinology|November 26, 2008
Analysis of the 206M polymorphic variant of the SLC26A6 gene encoding a Cl- oxalate transporter in patients with primary hyperparathyroidismS Corbetta, C Eller-Vainicher, M Frigerio, et al.
Journal of Endocrinological Investigation|May 13, 2005
Risk factors associated to kidney stones in primary hyperparathyroidismS Corbetta, A Baccarelli, A Aroldi, et al.
Revue Medicale De Bruxelles|September 17, 2015
[Recurrent episodes of brushite nephrolithiasis revealing primary hyperparathyroidism]I Simon, T Roumeguère, F Devuyst, et al.
The Journal of Clinical Endocrinology and Metabolism|August 15, 2001
Mutation of somatostatin receptor type 5 in an acromegalic patient resistant to somatostatin analog treatmentE Ballarè, L Persani, A G Lania, et al.
European Journal of Endocrinology|October 26, 2006
R990G polymorphism of the calcium-sensing receptor and renal calcium excretion in patients with primary hyperparathyroidismS Corbetta, C Eller-Vainicher, M Filopanti, et al.
Molecular Biosystems|March 21, 2013
Differential protein profiling of renal cell carcinoma urinary exosomesF Raimondo, L Morosi, S Corbetta, et al.
Endocrine-Related Cancer|November 21, 2009
Differential expression of microRNAs in human parathyroid carcinomas compared with normal parathyroid tissueS Corbetta, V Vaira, V Guarnieri, et al.
Journal of Endocrinological Investigation|June 5, 2009
Analysis of GNAS1 and PRKAR1A gene mutations in human cardiac myxomas not associated with multiple endocrine disordersG Mantovani, S Bondioni, S Corbetta, et al.
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