Showing results (31-40 of 42) with videos related to
Sort By:
Pageof 5
Clinical Endocrinology|April 9, 2008
The role of 18F-FDOPA and 18F-FDG-PET in the management of malignant and multifocal phaeochromocytomasD Taïeb, L Tessonnier, F Sebag, et al.International Journal of Andrology|March 6, 2010
RET gene mutations are not involved in the origin of human testicular seminomaN Chevalier, A Barlier, C Roche, et al.European Journal of Endocrinology|January 29, 2011
Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative formsR Reynaud, F Albarel, A Saveanu, et al.The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiencyS Vallette-Kasic, A Barlier, C Teinturier, et al.The Journal of Clinical Endocrinology and Metabolism|December 16, 2011
Phenotypic homogeneity and genotypic variability in a large series of congenital isolated ACTH-deficiency patients with TPIT gene mutationsC Couture, A Saveanu, A Barlier, et al.Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|January 23, 2016
GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone DeficiencyF Castinetti, A F Daly, C A Stratakis, et al.The Journal of Clinical Endocrinology and Metabolism|May 1, 2008
A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarismF Castinetti, A Saveanu, R Reynaud, et al.Journal of Neuroendocrinology|December 22, 2015
Combining Cadherin Expression with Molecular Markers Discriminates Invasiveness in Growth Hormone and Prolactin Pituitary AdenomasN Chauvet, N Romanò, A-C Meunier, et al.Clinical Endocrinology|November 3, 2010
Comparison of [¹¹¹In]pentetreotide-SPECT and [¹⁸F]FDOPA-PET in the localization of extra-adrenal paragangliomas: the case for a patient-tailored use of nuclear imaging modalitiesN Charrier, A Deveze, N Fakhry, et al.Pageof 5