Genetic causes of combined pituitary hormone deficiencies in humans
Author:
Publisher
Elsevier BV
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
Reference3 articles.
1. Genetic regulation of pituitary gland development in human and mouse;Kelberman;Endocr Rev,2009
2. A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarism;Castinetti;J Clin Endocrinol Metab,2008
3. Genetic screening of combined pituitary hormone deficiency: experience in 195 patients;Reynaud;J Clin Endocrinol Metab,2006
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1. Hypopituitarism in Patients with Blepharophimosis and FOXL2 Mutations;Hormone Research in Paediatrics;2020
2. Distinct pituitary hormone levels of 184 Chinese children and adolescents with multiple pituitary hormone deficiency: a single-centre study;BMC Pediatrics;2019-11-14
3. DIAGNOSIS OF ENDOCRINE DISEASE: Pituitary stalk interruption syndrome: etiology and clinical manifestations;European Journal of Endocrinology;2019-11
4. Pituitary Transcription Factor Mutations Leading to Hypopituitarism;Experientia Supplementum;2019
5. Hipopituitarismo. Una causa poco frecuente de retraso psicomotor;Neurología;2018-10
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