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Journal Abstract Search

101 related items for PubMed ID: 2989320

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  • 2. Activity of the stimulatory guanine nucleotide-binding protein is reduced in erythrocytes from patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism: biochemical, endocrine, and genetic analysis of Albright's hereditary osteodystrophy in six kindreds.
    Levine MA, Jap TS, Mauseth RS, Downs RW, Spiegel AM.
    J Clin Endocrinol Metab; 1986 Mar; 62(3):497-502. PubMed ID: 3003142
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  • 9. Father to son transmission of decreased Ns activity in pseudohypoparathyroidism type Ia.
    Van Dop C, Bourne HR, Neer RM.
    J Clin Endocrinol Metab; 1984 Nov; 59(5):825-8. PubMed ID: 6090498
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  • 10. Fibroblast defect in pseudohypoparathyroidism, type I: reduced activity of receptor-cyclase coupling protein.
    Bourne HR, Kaslow HR, Brickman AS, Farfel Z.
    J Clin Endocrinol Metab; 1981 Sep; 53(3):636-40. PubMed ID: 6267099
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  • 11. Selective resistance to parathyroid hormone in cultured skin fibroblasts from patients with pseudohypoparathyroidism type Ib.
    Silve C, Santora A, Breslau N, Moses A, Spiegel A.
    J Clin Endocrinol Metab; 1986 Apr; 62(4):640-4. PubMed ID: 3005354
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  • 12. Cutaneous ossification in Albright's hereditary osteodystrophy.
    Trüeb RM, Panizzon RG, Burg G.
    Dermatology; 1993 Apr; 186(3):205-9. PubMed ID: 8453149
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  • 14. Pseudohypoparathyroidism: inheritance and expression of deficient receptor-cyclase coupling protein activity.
    Fischer JA, Bourne HR, Dambacher MA, Tschopp F, De Meyer R, Devogelaer JP, Werder EA, Nagant De Deuxchaisnes C.
    Clin Endocrinol (Oxf); 1983 Dec; 19(6):747-54. PubMed ID: 6317236
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  • 15. Defect of receptor-cyclase coupling protein in pseudohypoparathyroidism.
    Farfel Z, Brickman AS, Kaslow HR, Brothers VM, Bourne HR.
    N Engl J Med; 1980 Jul 31; 303(5):237-42. PubMed ID: 6247654
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  • 17. Blunted plasma cyclic adenosine monophosphate response to isoproterenol in pseudohypoparathyroidism.
    Carlson HE, Brickman AS.
    J Clin Endocrinol Metab; 1983 Jun 31; 56(6):1323-6. PubMed ID: 6302127
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  • 18. Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy.
    Patten JL, Johns DR, Valle D, Eil C, Gruppuso PA, Steele G, Smallwood PM, Levine MA.
    N Engl J Med; 1990 May 17; 322(20):1412-9. PubMed ID: 2109828
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  • 19. Pseudohypoparathyroidism and idiopathic hypoparathyroidism: relationship between serum calcium and parathyroid hormone levels and urinary cyclic adenosine-3',5'-monophosphate response to parathyroid extract.
    Werder EA, Fischer JA, Illig R, Kind HP, Bernasconi S, Fanconi A, Prader A.
    J Clin Endocrinol Metab; 1978 Jun 17; 46(6):872-9. PubMed ID: 233700
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  • 20. [Cutaneous osteoma and Albright's hereditary osteodystrophy].
    Canillot S, Chouvet B, Besançon C, Perrot H.
    Ann Dermatol Venereol; 1994 Jun 17; 121(5):408-13. PubMed ID: 7702269
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