Hypoparathyroïdies

Revue du Rhumatisme (Edition Francaise)

Volumn 67, Issue SUPPL.2, 2000, Pages 91-94

  Essig, Marie ^a   Silve, Caroline ^a  

^a INSERM   (France)

Author keywords

Hypoparathyroidism

Indexed keywords

EID: 10444232853     PISSN: 11698330     EISSN: None     Source Type: Journal    
DOI: 10.1016/s1169-8330(00)80084-8     Document Type: Article

References (7)

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2. Basset JHD, Thakker RV Molecular genetics of disorders of calcium homeostasis. Baillières Clin Endocrinol Metab 1995 ; 9 : 581-608.
3. Silve C. Les hypoparathyroïdies et les pseudohypoparathyroïdies. In : Kuntz D. Les maladies métaboliques osseuses de l'adulte. Paris : Flammarion Médecine-Science ; 1996. p. 205-17.
4. Ahonen P, Mylärrniemi S, Sipilä I, Perheentupa J. Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients. N Engl J Med 1990; 322: 1829-36.
5. Scott HS, Heino M. Peterson P, Mittaz L, Lalioti MD, Betterle C, et al. Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different origins. Mol Endocrinol 1998 ; 12 : 1112-9.
6. De Luca F, Baron J. Molecular biology and clinical importance of the Ca(2 +) sensing receptor. Curr Opin Pediatr 1998 ; 10 : 435-40.
7. Tengan CH, Kiyomoto BH, Rocha MS, Tavares VL, Gabbai AA, Moraes CT. Mitochondrial encephalomyopathy and hypoparathyroidism associated with a duplication and a deletion of deoxyribonucleic acid. J Clin Endocrinol Metab 1998 ; 83 : 125-9.