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Journal Abstract Search

149 related items for PubMed ID: 23268667

  • 1. Images in clinical medicine. Albright's hereditary osteodystrophy.
    Rolla AR, Rodriguez-Gutierrez R.
    N Engl J Med; 2012 Dec 27; 367(26):2527. PubMed ID: 23268667
    [No Abstract] [Full Text] [Related]

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  • 4. Epigenetic defects of GNAS in patients with pseudohypoparathyroidism and mild features of Albright's hereditary osteodystrophy.
    de Nanclares GP, Fernández-Rebollo E, Santin I, García-Cuartero B, Gaztambide S, Menéndez E, Morales MJ, Pombo M, Bilbao JR, Barros F, Zazo N, Ahrens W, Jüppner H, Hiort O, Castaño L, Bastepe M.
    J Clin Endocrinol Metab; 2007 Jun 27; 92(6):2370-3. PubMed ID: 17405843
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  • 5. Pseudopseudohypoparathyroidism.
    Simpson C, Grove E, Houston BA.
    Lancet; 2015 Mar 21; 385(9973):1123. PubMed ID: 25484027
    [No Abstract] [Full Text] [Related]

  • 6. Albright's hereditary osteodystrophy and pseudohypoparathyroidism.
    Wilson LC, Hall CM.
    Semin Musculoskelet Radiol; 2002 Dec 21; 6(4):273-83. PubMed ID: 12541184
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  • 7. No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity.
    Izzi B, de Zegher F, Francois I, del Favero J, Goossens D, Wittevrongel C, Thys C, Van Geet C, Freson K.
    J Hum Genet; 2012 Apr 21; 57(4):277-9. PubMed ID: 22277900
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  • 8. 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 21; 76(1):45-8. PubMed ID: 16116826
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  • 9. Albright's hereditary osteodystrophy.
    Kapoor S, Gogia S, Paul R, Banerjee S.
    Indian J Pediatr; 2006 Feb 21; 73(2):153-6. PubMed ID: 16514227
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  • 10. [Genetic counseling in osteodystrophy Albright's syndrome. Part II. GNAS1 gene and encoded protein function, genetic forecast and treatment].
    Janusz L, Morawska J, Wasilewska E, Sierakowski S, Midro AT.
    Przegl Lek; 2010 Feb 21; 67(7):527-31. PubMed ID: 21387769
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  • 11. Mutations in exon 7 of the GTP-binding protein Gs alpha were not a common cause of pseudohypoparathyroidism with Albright's hereditary osteodystrophy in Japanese.
    Takeda K, Yokoyama M, Hashimoto K, Hiromatsu Y, Yamanaka H, Shimizu T, Sasaki M.
    Endocr J; 1997 Aug 21; 44(4):621-5. PubMed ID: 9447300
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  • 12. 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 21; 34(3):411-6. PubMed ID: 23281139
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  • 14. Albright hereditary osteodystrophy: report of a particular clinical phenotype caused by a novel GNAS mutation.
    Alvarez F, Kottler ML, Paul C, Gennero I, Salles JP, Mazereeuw-Hautier J.
    J Eur Acad Dermatol Venereol; 2010 Aug 21; 24(8):974-5. PubMed ID: 20015054
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  • 15. [Albright hereditary osteodystrophy: identification of a novel mutation in a family].
    Bastida Eizaguirre M, Iturbe Ortiz De Urbina R, Arto Urzainqui M, Ezquerra Larreina R, Escalada San Martín J.
    An Esp Pediatr; 2001 Jun 21; 54(6):598-600. PubMed ID: 11412411
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  • 16. 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 21; 81(4):1660-2. PubMed ID: 8636385
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  • 17. [Pseudopseudohypoparathyroidism and genomic imprinting].
    Minagawa M.
    Clin Calcium; 2007 Aug 21; 17(8):1229-33. PubMed ID: 17660620
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  • 18. Albright hereditary osteodystrophy: a rare case report.
    Goswami M, Verma M, Singh A, Grewal H, Kumar G.
    J Indian Soc Pedod Prev Dent; 2009 Aug 21; 27(3):184-8. PubMed ID: 19841552
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  • 19. [Epigenetics and pseudohypoparathyroidism].
    Richard N, Abéguilé G, Coudray N, Kottler ML.
    Pathol Biol (Paris); 2010 Oct 21; 58(5):367-71. PubMed ID: 19942373
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  • 20. [Cutaneous osteoma and Albright's hereditary osteodystrophy].
    Canillot S, Chouvet B, Besançon C, Perrot H.
    Ann Dermatol Venereol; 1994 Oct 21; 121(5):408-13. PubMed ID: 7702269
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