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 *

131 related articles for article (PubMed ID: 16789627)

  • 1. Pseudohypoparathyroidism: history of the disease.
    de Sanctis L
    J Pediatr Endocrinol Metab; 2006 May; 19 Suppl 2():627-33. PubMed ID: 16789627
    [No Abstract]   [Full Text] [Related]  

  • 2. [Pseudohypoparathyroidism].
    Yasuda T
    Nihon Rinsho; 2005 Oct; 63 Suppl 10():352-6. PubMed ID: 16279661
    [No Abstract]   [Full Text] [Related]  

  • 3. Pseudohypoparathyroidism type Ia from maternal but not paternal transmission of a Gsalpha gene mutation.
    Nakamoto JM; Sandstrom AT; Brickman AS; Christenson RA; Van Dop C
    Am J Med Genet; 1998 May; 77(4):261-7. PubMed ID: 9600732
    [TBL] [Abstract][Full Text] [Related]  

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

  • 5. Genetics of pseudohypoparathyroidism types Ia and Ic.
    Aldred MA
    J Pediatr Endocrinol Metab; 2006 May; 19 Suppl 2():635-40. PubMed ID: 16789628
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [GNAS1 gene abnormality in pseudohypoparathyroidism I a].
    Ozono K
    Clin Calcium; 2007 Aug; 17(8):1214-9. PubMed ID: 17660618
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pseudohypoparathyroidism: new insight into Gs alpha.
    Aldred MA
    Trends Mol Med; 2001 Jan; 7(1):8. PubMed ID: 11427993
    [No Abstract]   [Full Text] [Related]  

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

  • 9. 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]  

  • 10. 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]  

  • 11. Gs(alpha) mutations and imprinting defects in human disease.
    Weinstein LS; Chen M; Liu J
    Ann N Y Acad Sci; 2002 Jun; 968():173-97. PubMed ID: 12119276
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Subcutaneous calcifications and dysmorphic syndrome].
    Avenel G; Bernet J; Lahaxe L; Lévesque H; Marie I
    Rev Med Interne; 2010 Mar; 31(3):238-40. PubMed ID: 19329231
    [No Abstract]   [Full Text] [Related]  

  • 13. Pseudohypoparathyroidism and GNAS epigenetic defects: clinical evaluation of albright hereditary osteodystrophy and molecular analysis in 40 patients.
    Mantovani G; de Sanctis L; Barbieri AM; Elli FM; Bollati V; Vaira V; Labarile P; Bondioni S; Peverelli E; Lania AG; Beck-Peccoz P; Spada A
    J Clin Endocrinol Metab; 2010 Feb; 95(2):651-8. PubMed ID: 20061437
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Albright's hereditary osteodystrophy: historical credit.
    Levine MA
    Endocr Pract; 2000; 6(1):115. PubMed ID: 11428358
    [No Abstract]   [Full Text] [Related]  

  • 15. 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; 92(5):1764-8. PubMed ID: 17299070
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 92(6):2370-3. PubMed ID: 17405843
    [TBL] [Abstract][Full Text] [Related]  

  • 17. G protein Gs alpha (GNAS 1), the probable candidate gene for Albright hereditary osteodystrophy, is assigned to human chromosome 20q12-q13.2.
    Rao VV; Schnittger S; Hansmann I
    Genomics; 1991 May; 10(1):257-61. PubMed ID: 1904395
    [TBL] [Abstract][Full Text] [Related]  

  • 18. "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]  

  • 19. 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; 24(8):974-5. PubMed ID: 20015054
    [No Abstract]   [Full Text] [Related]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.