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Showing results (191-200 of 193) with videos related to

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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.
Endocrine Research|January 26, 2005
A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutationsS Vallette-Kasic, A M Pulichino, M Gueydan, et al.
Annales D'Endocrinologie|April 7, 2004
[Therapeutic strategies in somatotroph adenomas with extrasellar extension: role of the medical approach, a consensus study of the French Acromegaly Registry]Ph Jaquet, Ch Cortet-Rudelli, G Sassolas, et al.
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Showing results (191-200 of 193) with videos related to

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Pageof 20
You have reached the last page of results.This site can display upto 193 results.
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.
Endocrine Research|January 26, 2005
A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutationsS Vallette-Kasic, A M Pulichino, M Gueydan, et al.
Annales D'Endocrinologie|April 7, 2004
[Therapeutic strategies in somatotroph adenomas with extrasellar extension: role of the medical approach, a consensus study of the French Acromegaly Registry]Ph Jaquet, Ch Cortet-Rudelli, G Sassolas, et al.
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