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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 19329231)

  • 41. [Primary cutaneous osteoma in hereditary Albright osteodystrophy].
    Diercks K; Schulte K; Schuppe HC; Lehmann P
    Hautarzt; 1996 Sep; 47(9):673-5. PubMed ID: 8999021
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Pegvisomant for the treatment of gsp-mediated growth hormone excess in patients with McCune-Albright syndrome.
    Akintoye SO; Kelly MH; Brillante B; Cherman N; Turner S; Butman JA; Robey PG; Collins MT
    J Clin Endocrinol Metab; 2006 Aug; 91(8):2960-6. PubMed ID: 16720661
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Mutations in the Gs alpha gene causing hormone resistance.
    Mantovani G; Spada A
    Best Pract Res Clin Endocrinol Metab; 2006 Dec; 20(4):501-13. PubMed ID: 17161328
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Minireview: GNAS: normal and abnormal functions.
    Weinstein LS; Liu J; Sakamoto A; Xie T; Chen M
    Endocrinology; 2004 Dec; 145(12):5459-64. PubMed ID: 15331575
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Clinical and molecular findings in a family with the carbonic anhydrase II deficiency syndrome.
    Lotan D; Eisenkraft A; Jacobsson JM; Bar-Yosef O; Kleta R; Gal N; Raviv-Zilka L; Gore H; Anikster Y
    Pediatr Nephrol; 2006 Mar; 21(3):423-6. PubMed ID: 16382316
    [TBL] [Abstract][Full Text] [Related]  

  • 46. "A rare disorder, yes; an unimportant one, never".
    Olsen BR
    J Clin Invest; 1998 Apr; 101(8):1545-6. PubMed ID: 9541481
    [No Abstract]   [Full Text] [Related]  

  • 47. McCune-Albright syndrome: clinical and molecular evidence of mosaicism in an unusual giant patient.
    Tinschert S; Gerl H; Gewies A; Jung HP; Nürnberg P
    Am J Med Genet; 1999 Mar; 83(2):100-8. PubMed ID: 10190480
    [TBL] [Abstract][Full Text] [Related]  

  • 48. McCune-Albright syndrome in a boy may present with a monolateral macroorchidism as an early and isolated clinical manifestation.
    Arrigo T; Pirazzoli P; De Sanctis L; Leone O; Wasniewska M; Messina MF; De Luca F
    Horm Res; 2006; 65(3):114-9. PubMed ID: 16462147
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [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; 54(6):598-600. PubMed ID: 11412411
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Rare bone disorders reveal a key metabolic gene.
    Senior K
    Trends Mol Med; 2001 Feb; 7(2):45-6. PubMed ID: 11286735
    [No Abstract]   [Full Text] [Related]  

  • 51. A case of Albright's hereditary osteodystrophy-like syndrome complicated by several endocrinopathies: normal Gs alpha gene and chromosome 2q37.
    Sakaguchi H; Sanke T; Ohagi S; Iiri T; Nanjo K
    J Clin Endocrinol Metab; 1998 May; 83(5):1563-5. PubMed ID: 9589656
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Restoration of ovulation after unilateral ovariectomy in a woman with McCune-Albright syndrome: a case report.
    Lavoué V; Morcel K; Bouchard P; Sultan C; Massart C; Grall JY; Lumbroso S; Laurent MC
    Eur J Endocrinol; 2008 Jan; 158(1):131-4. PubMed ID: 18166827
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Resistance to the lipolytic action of epinephrine: a new feature of protein Gs deficiency.
    Carel JC; Le Stunff C; Condamine L; Mallet E; Chaussain JL; Adnot P; Garabédian M; Bougnères P
    J Clin Endocrinol Metab; 1999 Nov; 84(11):4127-31. PubMed ID: 10566660
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Activating Gsalpha mutations: analysis of 113 patients with signs of McCune-Albright syndrome--a European Collaborative Study.
    Lumbroso S; Paris F; Sultan C;
    J Clin Endocrinol Metab; 2004 May; 89(5):2107-13. PubMed ID: 15126527
    [TBL] [Abstract][Full Text] [Related]  

  • 55. G(s)alpha mutations in fibrous dysplasia and McCune-Albright syndrome.
    Weinstein LS
    J Bone Miner Res; 2006 Dec; 21 Suppl 2():P120-4. PubMed ID: 17229000
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Albright's hereditary osteodystrophy.
    Wilson LC; Trembath RC
    J Med Genet; 1994 Oct; 31(10):779-84. PubMed ID: 7837255
    [No Abstract]   [Full Text] [Related]  

  • 57. Unusual phenotypical variations in a boy with McCune-Albright syndrome.
    Mamkin I; Philibert P; Anhalt H; Ten S; Sultan C
    Horm Res Paediatr; 2010; 73(3):215-22. PubMed ID: 20197676
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism.
    De Sanctis L; Romagnolo D; Olivero M; Buzi F; Maghnie M; Scirè G; Crino A; Baroncelli GI; Salerno M; Di Maio S; Cappa M; Grosso S; Rigon F; Lala R; De Sanctis C; Dianzani I
    Pediatr Res; 2003 May; 53(5):749-55. PubMed ID: 12621129
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Madelung deformity in a girl with a novel and de novo mutation in the GNAS gene.
    Rump P; Jongbloed JD; Sikkema-Raddatz B; Mundlos S; Klopocki E; van der Luijt RB
    Am J Med Genet A; 2011 Oct; 155A(10):2566-70. PubMed ID: 21910239
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Regulation of spermatogenesis in McCune-Albright syndrome: lessons from a 15-year follow-up.
    De Luca F; Mitchell V; Wasniewska M; Arrigo T; Messina MF; Valenzise M; de Sanctis L; Lahlou N
    Eur J Endocrinol; 2008 Jun; 158(6):921-7. PubMed ID: 18505910
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.