1 |
John T, Pottis JR: Diseases of the parathyroid gland and other hyper and hypocalcemic disorders. In: Kasper DL, Braunwald E, Fauci AS, Hauser SL, Longo DL, Jameson JL, eds. Harrison's principles of Internal Medicine, 16th edition, New York, McGraw-Hill book company: 2005, p 2249
|
2 |
Tamada Y, Kanda S, Suzuki H, Tajima T, Nishiyama T: A pseudohypoparathyroidism type ia patient with normocalcemia. Endocr J 55: 169, 2008
DOI
ScienceOn
|
3 |
Ringel MD, Schwindinger WF, Levine MA: Clinical implications of genetic defects in g proteins the molecular basis of McCune-Albright syndrome and albright hereditary osteodystrophy. Medicine 75: 171, 1996
DOI
ScienceOn
|
4 |
Dezner M, Neelon FA, Lebovitz HE: Psuedohypoparathyroidism type II: A possible defect in the reception of the cyclic AMP signal. N Engl J Med 289: 1056, 1973
DOI
ScienceOn
|
5 |
Na GY, Kim YH, Min PK, Hwang SJ: A case of cutaneous ossification in pseudohypoparathyroidism. Korean J Dermatol 34: 842, 1996
|
6 |
Garavelli L, Pedori S, Zanacca C, Caselli G, Loiodice A, Mantovani G, Ammenti A, Virdis R, Banchini G: Albright's hereditary osteodystrophy (pseudohypoparathyroidism type Ia): Clinical case with a novel mutation of GNAS1. Acta Biomed 76: 45, 2005
|
7 |
Albujar PP, Hunter R, Dayan A: The brain in pseudohypoparathyroidism. Revisa de Neuro-Psiquiatria 66: 129, 2003
|
8 |
Albright F, Burnett CH, Smith PH, Parson W: Pseudohypoparathyroidism-an example of 'Seabright-Bantam syndrome'. Endocrinology 30:922, 1942
|