These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

274 related items for PubMed ID: 7702269

  • 1. [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]

  • 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 ossification in Albright's hereditary osteodystrophy.
    Trüeb RM, Panizzon RG, Burg G.
    Dermatology; 1993; 186(3):205-9. PubMed ID: 8453149
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Osteoma cutis in pseudohypoparathyroidism.
    Sethuraman G, Malhotra AK, Khaitan BK, Kumar R, Sharma VK, Kabra M, Singh MK.
    Clin Exp Dermatol; 2006 Mar; 31(2):225-7. PubMed ID: 16487097
    [Abstract] [Full Text] [Related]

  • 7. Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy.
    Patten JL, Johns DR, Valle D, Eil C, Gruppuso PA, Steele G, Smallwood PM, Levine MA.
    N Engl J Med; 1990 May 17; 322(20):1412-9. PubMed ID: 2109828
    [Abstract] [Full Text] [Related]

  • 8. 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 17; 81(4):1660-2. PubMed ID: 8636385
    [Abstract] [Full Text] [Related]

  • 9. [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 17; 54(6):598-600. PubMed ID: 11412411
    [Abstract] [Full Text] [Related]

  • 10. [Albright's hereditary osteodystrophy: report of three cases].
    Bujan MM, Cervini AB, Fano V, Pierini AM.
    Arch Argent Pediatr; 2010 Apr 17; 108(2):e24-7. PubMed ID: 20467695
    [Abstract] [Full Text] [Related]

  • 11. Albright's hereditary osteodystrophy.
    Boscherini B, Coen G, Bianchini G, Gallucci G, Ballanti P, Pasquino AM, Piccolo F, Manca Bitti ML, Spadoni GL.
    Acta Paediatr Scand; 1980 May 17; 69(3):305-9. PubMed ID: 6246707
    [Abstract] [Full Text] [Related]

  • 12. Activity of the stimulatory guanine nucleotide-binding protein is reduced in erythrocytes from patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism: biochemical, endocrine, and genetic analysis of Albright's hereditary osteodystrophy in six kindreds.
    Levine MA, Jap TS, Mauseth RS, Downs RW, Spiegel AM.
    J Clin Endocrinol Metab; 1986 Mar 17; 62(3):497-502. PubMed ID: 3003142
    [Abstract] [Full Text] [Related]

  • 13. 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 17; 21(3):551-68. PubMed ID: 4025387
    [Abstract] [Full Text] [Related]

  • 14. Albright's hereditary osteodystrophy.
    Kapoor S, Gogia S, Paul R, Banerjee S.
    Indian J Pediatr; 2006 Feb 17; 73(2):153-6. PubMed ID: 16514227
    [Abstract] [Full Text] [Related]

  • 15. 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 17; 73(9):845-50. PubMed ID: 18028761
    [Abstract] [Full Text] [Related]

  • 16. Recurrent ectopic calcification involving the maxillofacial skeleton: A potential harbinger of Albright's osteodystrophy.
    Cortes W, Gosain AK.
    J Craniofac Surg; 2006 Jan 17; 17(1):21-7. PubMed ID: 16432403
    [Abstract] [Full Text] [Related]

  • 17. Albright's hereditary osteodystrophy: a review.
    Fitch N.
    Am J Med Genet; 1982 Jan 17; 11(1):11-29. PubMed ID: 6278930
    [No Abstract] [Full Text] [Related]

  • 18. 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 17; 28(9):1012-6. PubMed ID: 9788040
    [Abstract] [Full Text] [Related]

  • 19. 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 17; 76(1):45-8. PubMed ID: 16116826
    [Abstract] [Full Text] [Related]

  • 20. [Albright's hereditary osteodystrophy I and cataract].
    Nicu C.
    Oftalmologia; 1995 Apr 17; 39(2):109-13. PubMed ID: 7766587
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.