Literature DB >> 4342294

Hereditary adrenocortical unresponsiveness to adrenocorticotropic hormone.

R P Kelch, S L Kaplan, E G Biglieri, G H Daniels, C J Epstein, M M Grumbach.   

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Year:  1972        PMID： 4342294     DOI： 10.1016/s0022-3476(72)80093-3

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  14 in total

1.  Leukodystrophy, skin hyperpigmentation, and adrenal atrophy: Siemerling-Creutzfeldt disease. Transmission through several generations in two families.

Authors:  H H Ropers; P Burmeister; W v Petrykowski; F Schindera
Journal:  Am J Hum Genet       Date:  1975-07       Impact factor: 11.025

2.  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

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.  Familial glucocorticoid deficiency, alacrimia and achalasia--Allgrove syndrome.

Authors:  M N Muranjan; M Gurav; T Surve; C T Deshmukh; B A Bharucha
Journal:  Indian J Pediatr       Date:  1999 Jan-Feb       Impact factor: 1.967

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.  Clinical presentation, growth, and pubertal development in Addison's disease.

Authors:  D B Grant; N D Barnes; M W Moncrieff; M O Savage
Journal:  Arch Dis Child       Date:  1985-10       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.  Familial glucocorticoid deficiency with a point mutation in the ACTH receptor: a case report.

Authors:  Chan Jong Kim; Young Jong Woo; Gu Hwan Kim; Han Wook Yoo
Journal:  J Korean Med Sci       Date:  2009-09-23       Impact factor: 2.153
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