BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 23268667)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 5. Pseudopseudohypoparathyroidism.
    Simpson C; Grove E; Houston BA
    Lancet; 2015 Mar; 385(9973):1123. PubMed ID: 25484027
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

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

  • 10. [Genetic counseling in osteodystrophy Albright's syndrome. Part II. GNAS1 gene and encoded protein function, genetic forecast and treatment].
    Janusz L; Morawska J; Wasilewska E; Sierakowski S; Midro AT
    Przegl Lek; 2010; 67(7):527-31. PubMed ID: 21387769
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Pseudohypoparathyroidism type Ia and pseudo-pseudohypoparathyroidism: the growing spectrum of GNAS inactivating mutations.
    Elli FM; deSanctis L; Ceoloni B; Barbieri AM; Bordogna P; Beck-Peccoz P; Spada A; Mantovani G
    Hum Mutat; 2013 Mar; 34(3):411-6. PubMed ID: 23281139
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel GNAS1 mutation in a German family with Albright's hereditary osteodystrophy.
    Klagge A; Jessnitzer B; Pfaeffle R; Stumvoll M; Fuhrer D
    Exp Clin Endocrinol Diabetes; 2010 Oct; 118(9):586-90. PubMed ID: 19856255
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [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]  

  • 16. 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]  

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

  • 18. 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]  

  • 19. [Epigenetics and pseudohypoparathyroidism].
    Richard N; Abéguilé G; Coudray N; Kottler ML
    Pathol Biol (Paris); 2010 Oct; 58(5):367-71. PubMed ID: 19942373
    [TBL] [Abstract][Full Text] [Related]  

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

    [Next]    [New Search]
    of 8.