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Journal Abstract Search

144 related items for PubMed ID: 6246707

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. [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; 111(12):1073-9. PubMed ID: 6529078
    [Abstract] [Full Text] [Related]

  • 3. [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
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Albright's hereditary osteodystrophy.
    Wilson LC.
    J Pediatr Endocrinol Metab; 2006 May; 19 Suppl 2():671-3. PubMed ID: 16789633
    [No Abstract] [Full Text] [Related]

  • 6. ALBRIGHT'S HEREDITARY OSTEODYSTROPHY IN A MOTHER AND DAUGHTER.
    HINKLE DO, TRAVIS LB, DODGE WF.
    Tex Rep Biol Med; 1965 May; 23():463-73. PubMed ID: 14336930
    [No Abstract] [Full Text] [Related]

  • 7. [Albright's hereditary osteodystrophy: report of three cases].
    Bujan MM, Cervini AB, Fano V, Pierini AM.
    Arch Argent Pediatr; 2010 Apr; 108(2):e24-7. PubMed ID: 20467695
    [Abstract] [Full Text] [Related]

  • 8.
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  • 9. Albright's hereditary osteodystrophy and pseudohypoparathyroidism.
    Wilson LC, Hall CM.
    Semin Musculoskelet Radiol; 2002 Dec; 6(4):273-83. PubMed ID: 12541184
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11.
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  • 12. Early manifestation of obesity and calcinosis cutis in infantile pseudohypoparathyroidism.
    Poomthavorn P, Zacharin M.
    J Paediatr Child Health; 2006 Dec; 42(12):821-3. PubMed ID: 17096721
    [Abstract] [Full Text] [Related]

  • 13. Albright's hereditary osteodystrophy.
    Kapoor S, Gogia S, Paul R, Banerjee S.
    Indian J Pediatr; 2006 Feb; 73(2):153-6. PubMed ID: 16514227
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. 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 27; 44(4):621-5. PubMed ID: 9447300
    [Abstract] [Full Text] [Related]

  • 16. Atrial septal defect associated with Albright's hereditary osteodystrophy and other anomalies: a clinical case.
    Picichè M, Castriota Scanderbeg A, Chiariello L, Levato ME, Tomai F, Pellegrino A.
    G Ital Cardiol; 1998 Sep 27; 28(9):1012-6. PubMed ID: 9788040
    [Abstract] [Full Text] [Related]

  • 17. [Albright's hereditary osteodystrophy: a case study].
    Tami L, Rherib C, Chefchaouni K, Knouni H, Barkat A.
    Pan Afr Med J; 2019 Sep 27; 34():190. PubMed ID: 32180864
    [Abstract] [Full Text] [Related]

  • 18. A disruptive mutation in exon 3 of the GNAS gene with albright hereditary osteodystrophy, normocalcemic pseudohypoparathyroidism, and selective long transcript variant Gsalpha-L deficiency.
    Thiele S, Werner R, Ahrens W, Hoppe U, Marschke C, Staedt P, Hiort O.
    J Clin Endocrinol Metab; 2007 May 27; 92(5):1764-8. PubMed ID: 17299070
    [Abstract] [Full Text] [Related]

  • 19. Imprinting in Albright's hereditary osteodystrophy.
    Davies SJ, Hughes HE.
    J Med Genet; 1993 Feb 27; 30(2):101-3. PubMed ID: 8383205
    [Abstract] [Full Text] [Related]

  • 20. Albright's hereditary osteodystrophy: a review.
    Fitch N.
    Am J Med Genet; 1982 Jan 27; 11(1):11-29. PubMed ID: 6278930
    [No Abstract] [Full Text] [Related]

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