Literature DB >> 4302512

The syndrome of congenital adrenocortical unresponsiveness to ACTH. Report of six cases.

C J Migeon, E M Kenny, A Kowarski, C A Snipes, J S Spaulding, J W Finkelstein, R M Blizzard.   

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Year:  1968        PMID： 4302512     DOI： 10.1203/00006450-196811000-00008

Source DB:  PubMed          Journal:  Pediatr Res        ISSN： 0031-3998            Impact factor:   3.756


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  15 in total

1.  Selective ACTH insensitivity associated with autonomic nervous system disorders and sensory polyneuropathy.

Authors:  M Dumić; A Radica; A Jusić; N Stefanović; Z Murko
Journal:  Eur J Pediatr       Date:  1987-11       Impact factor: 3.183

2.  Isolated glucocorticoid deficiency: metabolic and endocrine studies in a 5-year-old boy.

Authors:  G Soltesz; M J Dillon; P A Jenkins; A Moore; A Aynsley-Green
Journal:  Eur J Pediatr       Date:  1985-03       Impact factor: 3.183

Review 3.  Role of proopiomelanocortin-derived peptides and their receptors in the osteoarticular system: from basic to translational research.

Authors:  Markus Böhm; Susanne Grässel
Journal:  Endocr Rev       Date:  2012-06-26       Impact factor: 19.871

4.  Familial glucocorticoid deficiency. Studies of diagnosis and pathogenesis.

Authors:  D Thistlethwaite; J A Darling; R Fraser; P A Mason; L H Rees; R A Harkness
Journal:  Arch Dis Child       Date:  1975-04       Impact factor: 3.791

5.  Molecular identification of the human melanocortin-2 receptor responsible for ligand binding and signaling.

Authors:  Min Chen; Charles J Aprahamian; Robert A Kesterson; Carroll M Harmon; Yingkui Yang
Journal:  Biochemistry       Date:  2007-09-18       Impact factor: 3.162

6.  Familial adrenocorticotropin unresponsiveness associated with alacrima and achalasia: biochemical and molecular studies in two siblings with clinical heterogeneity.

Authors:  C Heinrichs; C Tsigos; J Deschepper; R Drews; R Collu; C Dugardeyn; P Goyens; G E Ghanem; D Bosson; G P Chrousos
Journal:  Eur J Pediatr       Date:  1995-03       Impact factor: 3.183

7.  Neurological and adrenal dysfunction in the adrenal insufficiency/alacrima/achalasia (3A) syndrome.

Authors:  D B Grant; N D Barnes; M Dumic; M Ginalska-Malinowska; P J Milla; W von Petrykowski; R J Rowlatt; R Steendijk; J H Wales; E Werder
Journal:  Arch Dis Child       Date:  1993-06       Impact factor: 3.791

8.  Hereditary isolated glucocorticoid deficiency is associated with abnormalities of the adrenocorticotropin receptor gene.

Authors:  C Tsigos; K Arai; W Hung; G P Chrousos
Journal:  J Clin Invest       Date:  1993-11       Impact factor: 14.808

9.  Adrenocorticotropic hormone insensitivity associated with autonomic nervous system disorders.

Authors:  M Dumić; A Radica; Z Sabol; V Plavsić; L Brkljacić; V Sarnavka; J Vuković
Journal:  Eur J Pediatr       Date:  1991-08       Impact factor: 3.183

10.  Phenotypic characteristics of familial glucocorticoid deficiency (FGD) type 1 and 2.

Authors:  Teng-Teng L L Chung; Li F Chan; Louise A Metherell; Adrian J L Clark
Journal:  Clin Endocrinol (Oxf)       Date:  2009-06-24       Impact factor: 3.478
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