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Journal Abstract Search

133 related items for PubMed ID: 14336930

  • 21.
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  • 24. Familial Albright's hereditary osteodystrophy with hypoparathyroidism: normal structural Gs alpha gene.
    Shapira H, Friedman E, Mouallem M, Farfel Z.
    J Clin Endocrinol Metab; 1996 Apr; 81(4):1660-2. PubMed ID: 8636385
    [Abstract] [Full Text] [Related]

  • 25. [Albright's hereditary osteodystrophy with multiple cutaneous osteomas].
    Lorette G, Valat JP, Gatti P, Fetissoff F, Arbeille B, Boistard C, Moraine C.
    Ann Dermatol Venereol; 1984 Apr; 111(12):1073-9. PubMed ID: 6529078
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  • 27. [Physiopathology and therapy of pseudohypoparathyroidism and pseudopseudohypoparathyroidism].
    Yamamoto M.
    Nihon Naika Gakkai Zasshi; 1999 Jul 10; 88(7):1238-44. PubMed ID: 10465971
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  • 28. [Albright's hereditary osteodystrophy. Apropos of a familial case].
    Gaudier B, Ponte C, Leplat R, Bonte C, Deroubaix P.
    Pediatrie; 1966 Jul 10; 21(3):273-98. PubMed ID: 5930417
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  • 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 10; 76(1):45-8. PubMed ID: 16116826
    [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 24; 2013():. PubMed ID: 23814007
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  • 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 24; 148(4):463-8. PubMed ID: 12656668
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  • 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 24; 52(2):127-31. PubMed ID: 21605097
    [Abstract] [Full Text] [Related]

  • 35. Albright's hereditary osteodystrophy with cutaneous bone formation.
    Eyre WG, Reed WB.
    Arch Dermatol; 1971 Dec 24; 104(6):634-42. PubMed ID: 5002252
    [No 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 24; 35(6):380-4. PubMed ID: 7566382
    [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 24; 62(6):529-33. PubMed ID: 11845029
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  • 38. [Albright's hereditary osteodystrophy: a case study].
    Tami L, Rherib C, Chefchaouni K, Knouni H, Barkat A.
    Pan Afr Med J; 2019 Dec 24; 34():190. PubMed ID: 32180864
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  • 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 24; 34(3):411-6. PubMed ID: 23281139
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  • 40. [On the genetics of Albright's hereditary osteodystrophy].
    Spranger J, Rohwedder J.
    Med Welt; 1965 Oct 09; 41():2308-12. PubMed ID: 5864767
    [No Abstract] [Full Text] [Related]

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