BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 20738794)

  • 1. Albright hereditary osteodystrophy.
    Stieler K; Schnabel D; Atugoda S; Sterry W; Blume-Peytavi U
    Pediatr Dermatol; 2011; 28(2):135-7. PubMed ID: 20738794
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. 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]  

  • 4. 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]  

  • 5. A maternal epimutation of GNAS leads to Albright osteodystrophy and parathyroid hormone resistance.
    Mariot V; Maupetit-Méhouas S; Sinding C; Kottler ML; Linglart A
    J Clin Endocrinol Metab; 2008 Mar; 93(3):661-5. PubMed ID: 18182455
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Selective deficiency of Gsalpha and the possible role of alternative gene products of GNAS in Albright hereditary osteodystrophy and pseudohypoparathyroidism type Ia.
    Thiele S; Werner R; Ahrens W; Hübner A; Hinkel KG; Höppner W; Igl B; Hiort O
    Exp Clin Endocrinol Diabetes; 2010 Feb; 118(2):127-32. PubMed ID: 19658058
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pseudohypoparathyroidism-Albright hereditary osteodystrophy.
    Rastogi S; Gupta S; Misra PK; Rastogi D
    Indian J Pediatr; 1998; 65(3):477-80. PubMed ID: 10772004
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. 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]  

  • 13. 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]  

  • 14. A rare case of 2q37 microdeletion with Albright hereditary osteodystrophy-like phenotype.
    Simşek-Kiper PO; Utine GE; Alanay Y; Aktaş D; Alikaşifoğlu M; Boduroğlu K
    Turk J Pediatr; 2011; 53(5):558-60. PubMed ID: 22272459
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. A mouse model of albright hereditary osteodystrophy generated by targeted disruption of exon 1 of the Gnas gene.
    Germain-Lee EL; Schwindinger W; Crane JL; Zewdu R; Zweifel LS; Wand G; Huso DL; Saji M; Ringel MD; Levine MA
    Endocrinology; 2005 Nov; 146(11):4697-709. PubMed ID: 16099856
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Pseudohypoparathyroidism Ia with Evans syndrome.
    Pavone P; Praticò AD; Castellano-Chiodo D; Ruggieri M
    J Pediatr Hematol Oncol; 2008 Aug; 30(8):628-30. PubMed ID: 18799944
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Clinical implications of genetic defects in G proteins. The molecular basis of McCune-Albright syndrome and Albright hereditary osteodystrophy.
    Ringel MD; Schwindinger WF; Levine MA
    Medicine (Baltimore); 1996 Jul; 75(4):171-84. PubMed ID: 8699958
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.