Central hypocortisolism as part of combined pituitary hormone deficiency due to mutations of PROP-1 gene

scientific article

Central hypocortisolism as part of combined pituitary hormone deficiency due to mutations of PROP-1 gene is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1530/EJE.0.1430347
P698PubMed publication ID11022176
P5875ResearchGate publication ID12302003

P2093author name stringP Beck-Peccoz
C Asteria
J Abucham
J H Oliveira
P433issue3
P304page(s)347-352
P577publication date2000-09-01
P1433published inEuropean Journal of EndocrinologyQ3060778
P1476titleCentral hypocortisolism as part of combined pituitary hormone deficiency due to mutations of PROP-1 gene
P478volume143

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cites work (P2860)
Q64946519A Large PROP1 Gene Deletion in a Turkish Pedigree.
Q48142992Acquired prolactin deficiency in patients with disorders of the hypothalamic-pituitary axis
Q42443191Adrenocorticotrope deficiency with clinical evidence for late onset in combined pituitary hormone deficiency caused by a homozygous 301-302delAG mutation of the PROP1 gene
Q31055358Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion.
Q38868271Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes.
Q28082581Genetic Approaches to Hypothalamic-Pituitary-Adrenal Axis Regulation
Q33590141Genetic regulation of pituitary gland development in human and mouse
Q34430600Gradual loss of ACTH due to a novel mutation in LHX4: comprehensive mutation screening in Japanese patients with congenital hypopituitarism
Q49271387Managing Transition in Patients Treated with Growth Hormone
Q51968780Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency.
Q34367104Novel insights into the aetiology and pathogenesis of hypopituitarism
Q28255040Pituitary transcription factors: from congenital deficiencies to gene therapy
Q80385516The natural history of the R120C PROP1 mutation reveals a wide phenotypic variability in two untreated adult brothers with combined pituitary hormone deficiency
Q37905532The role of homeodomain transcription factors in heritable pituitary disease
Q36793669The role of transcription factors implicated in anterior pituitary development in the aetiology of congenital hypopituitarism
Q73666935Two new PROP1 gene mutations responsible for compound pituitary hormone deficiency

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