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 *

135 related articles for article (PubMed ID: 19841552)

  • 1. Albright hereditary osteodystrophy: a rare case report.
    Goswami M; Verma M; Singh A; Grewal H; Kumar G
    J Indian Soc Pedod Prev Dent; 2009; 27(3):184-8. PubMed ID: 19841552
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. Unique skin changes in a case of Albright hereditary osteodystrophy caused by a rare GNAS1 mutation.
    Klaassens M; Blom EW; Schrander JJ; Ris-Stalpers C; Nieuwenhuijzen Kruseman AC; van Steensel MA; Schrander-Stumpel CT
    Br J Dermatol; 2010 Mar; 162(3):690-4. PubMed ID: 19863504
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Calcinosis cutis in Albright hereditary osteodystrophy: pseudohypoparathyroidism type Ia].
    Fölster-Holst R; Riepe FG; Ahrens W; Möller M; Brasch J; Partsch CJ; Hiort O; Sippell WG
    Hautarzt; 2006 Oct; 57(10):893-7. PubMed ID: 16270203
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of two novel deletion mutations within the Gs alpha gene (GNAS1) in Albright hereditary osteodystrophy.
    Yu D; Yu S; Schuster V; Kruse K; Clericuzio CL; Weinstein LS
    J Clin Endocrinol Metab; 1999 Sep; 84(9):3254-9. PubMed ID: 10487696
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Oral manifestations of Albright hereditary osteodystrophy: a case report.
    Gomes MF; Camargo AM; Sampaio TA; Graziozi MA; Armond MC
    Rev Hosp Clin Fac Med Sao Paulo; 2002; 57(4):161-6. PubMed ID: 12244336
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 81(4):1660-2. PubMed ID: 8636385
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Albright hereditary osteodystrophy and del(2) (q37.3) in four unrelated individuals.
    Phelan MC; Rogers RC; Clarkson KB; Bowyer FP; Levine MA; Estabrooks LL; Severson MC; Dobyns WB
    Am J Med Genet; 1995 Jul; 58(1):1-7. PubMed ID: 7573148
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new heterozygous mutation (L338N) in the human Gsalpha (GNAS1) gene as a cause for congenital hypothyroidism in Albright's hereditary osteodystrophy.
    Pohlenz J; Ahrens W; Hiort O
    Eur J Endocrinol; 2003 Apr; 148(4):463-8. PubMed ID: 12656668
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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; 57(4):277-9. PubMed ID: 22277900
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. [Pseudopseudohypoparathyroidism and genomic imprinting].
    Minagawa M
    Clin Calcium; 2007 Aug; 17(8):1229-33. PubMed ID: 17660620
    [TBL] [Abstract][Full Text] [Related]  

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

  • 16. 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]  

  • 17. [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]  

  • 18. Constitutional deletion of chromosome 20q in two patients affected with albright hereditary osteodystrophy.
    Aldred MA; Aftimos S; Hall C; Waters KS; Thakker RV; Trembath RC; Brueton L
    Am J Med Genet; 2002 Nov; 113(2):167-72. PubMed ID: 12407707
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.