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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.
Archives of Disease in Childhood|January 6, 1999
Long-term follow up of 69 patients treated for optic pathway tumours before the chemotherapy eraC Cappelli, J Grill, M Raquin, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndromeS Hadj-Rabia, R Salomon, A Pelet, 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 Immunology (Baltimore, Md. : 1950)|March 12, 2025
Differential shaping of T cell responses elicited by heterologous ChAd68/self-amplifying mRNA SIV vaccine in macaques in combination with αCTLA4, αPD-1, or FLT3R agonistAmy R Rappaport, Elena Bekerman, Gregory R Boucher, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 1, 2005
A nationwide study of granulosa cell tumors in pre- and postpubertal girls: missed diagnosis of endocrine manifestations worsens prognosisN Kalfa, C Patte, D Orbach, et al.
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