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2. Differential diagnosis in young women with oligomenorrhea and the pseudo-pseudohypoparathyroidism variant of Albright's hereditary osteodystrophy. Halal F; Van Dop C; Lord J Am J Med Genet; 1985 Jul; 21(3):551-68. PubMed ID: 4025387 [TBL] [Abstract][Full Text] [Related]
4. [Albright's hereditary osteodystrophy I and cataract]. Nicu C Oftalmologia; 1995; 39(2):109-13. PubMed ID: 7766587 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. [On the genetics of Albright's hereditary osteodystrophy]. Spranger J; Rohwedder J Med Welt; 1965 Oct; 41():2308-12. PubMed ID: 5864767 [No Abstract] [Full Text] [Related]
7. [Cutaneous osteoma and Albright's hereditary osteodystrophy]. Canillot S; Chouvet B; Besançon C; Perrot H Ann Dermatol Venereol; 1994; 121(5):408-13. PubMed ID: 7702269 [TBL] [Abstract][Full Text] [Related]
14. Albright's hereditary osteodystrophy. Report of a family with studies of bone remodeling. Arnstein AR; Frame B; Frost HM; Bock MA Ann Intern Med; 1966 May; 64(5):996-1008. PubMed ID: 5933794 [No Abstract] [Full Text] [Related]
15. Military service and pseudopseudohypoparathyroidism: recognizing red flags for rare medical conditions. Riggs JE Mil Med; 1997 Jul; 162(7):510-2. PubMed ID: 9232985 [TBL] [Abstract][Full Text] [Related]
16. Albright's hereditary osteodystrophy with extensive heterotopic ossification of the oral and maxillofacial region: how fetuin research may help a seemingly impossible condition. DuVal MG; Davidson S; Ho A; Cohen R; Park M; Nourian S; Baker G; Sándor GK J Can Dent Assoc; 2007 Nov; 73(9):845-50. PubMed ID: 18028761 [TBL] [Abstract][Full Text] [Related]
17. Partial hypopituitarism, hypoglycemia, and hyperlipemia in Albright's dystrophy. Sareen CK; Ruvalcaba RH; Kelley VC Am J Ment Defic; 1974 Mar; 78(5):550-5. PubMed ID: 4820203 [No Abstract] [Full Text] [Related]
18. [Albright's hereditary osteodystrophy. Apropos of a familial case]. Gaudier B; Ponte C; Leplat R; Bonte C; Deroubaix P Pediatrie; 1966; 21(3):273-98. PubMed ID: 5930417 [No Abstract] [Full Text] [Related]
19. Brachydactyly mental retardation syndrome in differential diagnosis of pseudopseudohypoparathyroidism. Hacıhamdioğlu B; Arslan M; Sarı E; Kurtçu K; Yesilkaya E J Pediatr Endocrinol Metab; 2013; 26(7-8):793-5. PubMed ID: 23645122 [TBL] [Abstract][Full Text] [Related]
20. [Albright's hereditary osteodystrophy. 3 new cases with thyrocalcitonin and calcium 45 tests]. Bader JC; Canlorbe P; Lambertz J; Poitout M; Lelong M Ann Pediatr (Paris); 1968 Apr; 15(4):1061-73. PubMed ID: 5743017 [No Abstract] [Full Text] [Related] [Next] [New Search]