These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
136 related articles for article (PubMed ID: 4359274)
1. Probable autosomal recessive inheritance in a family with Albright's hereditary osteodystrophy and an evaluation of the genetics of the disorder. Cederbaum SD; Lippe BM Am J Hum Genet; 1973 Nov; 25(6):638-45. PubMed ID: 4359274 [No Abstract] [Full Text] [Related]
2. 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 [TBL] [Abstract][Full Text] [Related]
4. Effective long-term treatment of pseudohypoparathyroidism with oral 1alpha-hydroxy- and 1,25-dihydroxy-cholecalciferol. Werder EA; Kind HP; Egert F; Fischer JA; Prader A J Pediatr; 1976 Aug; 89(2):266-8. PubMed ID: 940021 [No Abstract] [Full Text] [Related]
5. Imprinting in Albright's hereditary osteodystrophy. Davies SJ; Hughes HE J Med Genet; 1993 Feb; 30(2):101-3. PubMed ID: 8383205 [TBL] [Abstract][Full Text] [Related]
6. Plasma cyclic-AMP response to parathyroid hormone in Turner's syndrome and Albright's hereditary osteodystrophy. Ashby JP; Renton WB; MacPherson JN; Price WH; Abbott SR Clin Endocrinol (Oxf); 1979 Jun; 10(6):553-6. PubMed ID: 225067 [TBL] [Abstract][Full Text] [Related]
7. Normocalcemic pseudohypoparathyroidism (Type II). Patel ZM; Ambani LM; Shah P; Sheth AR; Merchant SM Indian Pediatr; 1981 Nov; 18(11):828-32. PubMed ID: 6281182 [No Abstract] [Full Text] [Related]
8. 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 [TBL] [Abstract][Full Text] [Related]
9. Hyperthyrotropinemia in a neonate with normal thyroid hormone levels: the earliest diagnostic clue for pseudohypoparathyroidism. Yokoro S; Matsuo M; Ohtsuka T; Ohzeki T Biol Neonate; 1990; 58(2):69-72. PubMed ID: 2171682 [TBL] [Abstract][Full Text] [Related]
10. Cutaneous ossification in Albright's hereditary osteodystrophy. Trüeb RM; Panizzon RG; Burg G Dermatology; 1993; 186(3):205-9. PubMed ID: 8453149 [TBL] [Abstract][Full Text] [Related]
11. Pseudohypoparathyroidism: report on a family with four affected sisters. Kinard RE; Walton JE; Buckwalter JA Arch Intern Med; 1979 Feb; 139(2):204-7. PubMed ID: 219790 [TBL] [Abstract][Full Text] [Related]
13. Phenotypic and molecular genetic aspects of pseudohypoparathyroidism type Ib in a Greek kindred: evidence for enhanced uric acid excretion due to parathyroid hormone resistance. Laspa E; Bastepe M; Jüppner H; Tsatsoulis A J Clin Endocrinol Metab; 2004 Dec; 89(12):5942-7. PubMed ID: 15579741 [TBL] [Abstract][Full Text] [Related]
16. Pseudohypoparathyroidism type II: a possible defect in the reception of the cyclic AMP signal. Drezner M; Neelon FA; Lebovitz HE N Engl J Med; 1973 Nov; 289(20):1056-60. PubMed ID: 4355058 [No Abstract] [Full Text] [Related]
17. Albright's osteodystrophy in a patient with renal hypercalciuria. Moses AM; Notman DD J Clin Endocrinol Metab; 1979 Nov; 49(5):794-7. PubMed ID: 226562 [TBL] [Abstract][Full Text] [Related]
18. Urinary 3'5' cyclic AMP. Diagnostic test in pseudohypoparathyroidism. Tze WJ; Saunders J; Drummond GI Arch Dis Child; 1975 Aug; 50(8):656-8. PubMed ID: 173244 [TBL] [Abstract][Full Text] [Related]
19. Albright's hereditary osteodystrophy: a review. Fitch N Am J Med Genet; 1982 Jan; 11(1):11-29. PubMed ID: 6278930 [No Abstract] [Full Text] [Related]
20. [Albright's hereditary osteodystrophy: a case study]. Tami L; Rherib C; Chefchaouni K; Knouni H; Barkat A Pan Afr Med J; 2019; 34():190. PubMed ID: 32180864 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]