Current approaches for deciphering the molecular basis of combined anterior pituitary hormone deficiency in humans
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Molecular Biology,Biochemistry
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1. Extreme Short Stature and Severe Neurological Impairment in a 17-Year-Old Male With Untreated Combined Pituitary Hormone Deficiency Due to POU1F1 Mutation;Frontiers in Endocrinology;2019-06-27
2. Deficit in Anterior Pituitary Function and Variable Immune Deficiency (DAVID) in Children Presenting with Adrenocorticotropin Deficiency and Severe Infections;The Journal of Clinical Endocrinology & Metabolism;2012-01
3. Système IGF, carrefour de diverses pathologies;Aspects biologiques, moléculaires et cliniques de l’axe GH/IGF-I;2012
4. A novel POU1F1 mutation (p.Thr168IlefsX7) associated with an early and severe form of combined pituitary hormone deficiency: functional analysis and follow-up from infancy to adulthood;Clinical Endocrinology;2011-07-06
5. A Novel Missense Mutation (P366T) of the LHX4 Gene Causes Severe Combined Pituitary Hormone Deficiency with Pituitary Hypoplasia, Ectopic Posterior Lobe and a Poorly Developed Sella Turcica;Endocrine Journal;2007
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