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26. Albright's hereditary osteodystrophy: an entity to recognize. Maduro AI; Pinto Saraiva A; Pimenta Rodrigues O; Marques M; B Sousa S; Malcata A; Perez de Nanclares G; Serra S Rheumatology (Oxford); 2022 Nov; 61(11):e356-e357. PubMed ID: 35551352 [No Abstract] [Full Text] [Related]
27. [Physiopathology and therapy of pseudohypoparathyroidism and pseudopseudohypoparathyroidism]. Yamamoto M Nihon Naika Gakkai Zasshi; 1999 Jul; 88(7):1238-44. PubMed ID: 10465971 [No Abstract] [Full Text] [Related]
28. [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]
29. Albright's hereditary osteodystrophy (pseudohypoparathyroidism type Ia): clinical case with a novel mutation of GNAS1. Garavelli L; Pedori S; Zanacca C; Caselli G; Loiodice A; Mantovani G; Ammenti A; Virdis R; Banchini G Acta Biomed; 2005 Apr; 76(1):45-8. PubMed ID: 16116826 [TBL] [Abstract][Full Text] [Related]
30. Sinus pauses and high-grade atrioventricular block in Albright's hereditary osteodystrophy with pseudopseudohypoparathyroidism. Rahmat N; Venables P BMJ Case Rep; 2013 Jun; 2013():. PubMed ID: 23814007 [TBL] [Abstract][Full Text] [Related]
31. 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]
32. [PSEUDOHYPOPARATHYROIDISM. A CASE REPORT CONTRIBUTION AND CRITICAL OBSERVATIONS ON THE PATHOGENESIS]. LINS H; SOLBACH HG; REINWEIN D Z Klin Med; 1964 Jun; 158():143-55. PubMed ID: 14250363 [No Abstract] [Full Text] [Related]
33. A new heterozygous mutation (L338N) in the human Gsalpha (GNAS1) gene as a cause for congenital hypothyroidism in Albright's hereditary osteodystrophy. Pohlenz J; Ahrens W; Hiort O Eur J Endocrinol; 2003 Apr; 148(4):463-8. PubMed ID: 12656668 [TBL] [Abstract][Full Text] [Related]
34. Three cases of osteoma cutis occurring in infancy. A brief overview of osteoma cutis and its association with pseudo-pseudohypoparathyroidism. Ward S; Sugo E; Verge CF; Wargon O Australas J Dermatol; 2011 May; 52(2):127-31. PubMed ID: 21605097 [TBL] [Abstract][Full Text] [Related]
36. Hemifacial spasm in Albright's hereditary osteodystrophy with pseudopseudohypoparathyroidism and nephrogenic diabetes insipidus--case report. Oyama H; Kida Y; Tanaka T; Iwakoshi T; Niwa M; Kitamura R; Kobayashi T Neurol Med Chir (Tokyo); 1995 Jun; 35(6):380-4. PubMed ID: 7566382 [TBL] [Abstract][Full Text] [Related]
37. [Pseudohypoparathyroidism or hypoparathyroidism? A misleading clinical presentation]. Derrien C; Odent S; Henry C; De La Villemarque R; Poirier JY; Maugendre D Ann Endocrinol (Paris); 2001 Dec; 62(6):529-33. PubMed ID: 11845029 [TBL] [Abstract][Full Text] [Related]
38. [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]
39. Pseudohypoparathyroidism type Ia and pseudo-pseudohypoparathyroidism: the growing spectrum of GNAS inactivating mutations. Elli FM; deSanctis L; Ceoloni B; Barbieri AM; Bordogna P; Beck-Peccoz P; Spada A; Mantovani G Hum Mutat; 2013 Mar; 34(3):411-6. PubMed ID: 23281139 [TBL] [Abstract][Full Text] [Related]
40. [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] [Previous] [Next] [New Search]