Recent advances in the molecular genetics of congenital and acquired primary adrenocortical failure
Open Access
- 1 October 2000
- journal article
- review article
- Published by Wiley in Clinical Endocrinology
- Vol. 53 (4) , 403-418
- https://doi.org/10.1046/j.1365-2265.2000.01116.x
Abstract
No abstract availableKeywords
This publication has 108 references indexed in Scilit:
- A cytotoxic T lymphocyte antigen‐4 (CTLA‐4) gene polymorphism is associated with autoimmune Addison's disease in English patientsClinical Endocrinology, 1998
- Adrenoleukodystrophy Protein-Deficient Mice Represent Abnormality of Very Long Chain Fatty Acid MetabolismBiochemical and Biophysical Research Communications, 1997
- Major histocompatibility complex class II and III in Addison's disease MHC alleles do not predict autoantibody specificity and 21-hydroxylase gene polymorphism has no independent role in disease susceptibilityHuman Immunology, 1994
- Reversal of Early Neurologic and Neuroradiologic Manifestations of X-Linked Adrenoleukodystrophy by Bone Marrow TransplantationNew England Journal of Medicine, 1990
- Clinical Variation of Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy (APECED) in a Series of 68 PatientsNew England Journal of Medicine, 1990
- Adrenomyeloneuropathy Presenting as Addison's Disease in ChildhoodNew England Journal of Medicine, 1990
- Congenital Adrenal HyperplasiaNew England Journal of Medicine, 1987
- Two Types of Autoimmune Addisonʼs Disease Associated with Different Polyglandular Autoimmune (PGA) SyndromesMedicine, 1981
- HLA Type and Occurrence of Disease in Familial Polyglandular FailureNew England Journal of Medicine, 1978
- Luteinizing hormone deficiency in hereditary congenital adrenal hypoplasiaThe Journal of Pediatrics, 1975