Literature DB >> 13616862

Familial Addison's disease; case reports of two sisters with corticoid deficiency unassociated with hypoaldosteronism.

T H SHEPARD, B H LANDING, D G MASON.   

Abstract

Entities:  

Keywords:  ADDISON'S DISEASE/in infant and child

Mesh：

Substances：

Year:  1959        PMID： 13616862

Source DB:  PubMed          Journal:  AMA J Dis Child        ISSN： 0096-6916


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  30 in total

1.  Familial glucocorticoid deficiency syndromes.

Authors:  Frederich C Luft
Journal:  J Mol Med (Berl)       Date:  2002-07       Impact factor: 4.599

2.  Adrenal Cortical Hypoplasia in Siblings.

Authors:  J F Boyd; A M Macdonald
Journal:  Arch Dis Child       Date:  1960-12       Impact factor: 3.791

3.  Addison's disease in a 6-year-old boy.

Authors:  G W PEARSON
Journal:  Br Med J       Date:  1962-04-14

4.  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

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.  Association of polymorphisms in the melanocortin receptor type 2 (MC2R, ACTH receptor) gene with heroin addiction.

Authors:  Dmitri Proudnikov; Sara Hamon; Jurg Ott; Mary Jeanne Kreek
Journal:  Neurosci Lett       Date:  2008-02-26       Impact factor: 3.046

8.  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

9.  Isolated Addison's disease is unlikely to be caused by mutations in MC2R, MRAP or STAR, three genes responsible for familial glucocorticoid deficiency.

Authors:  R P Dias; L F Chan; L A Metherell; S H S Pearce; A J L Clark
Journal:  Eur J Endocrinol       Date:  2009-11-10       Impact factor: 6.664

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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