BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 20738794)

  • 21. 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]  

  • 22. Cutaneous and superficial soft tissue lesions associated with Albright hereditary osteodystrophy: clinicopathological and molecular genetic study of 4 cases, including a novel mutation of the GNAS gene.
    Kacerovska D; Nemcova J; Pomahacova R; Michal M; Kazakov DV
    Am J Dermatopathol; 2008 Oct; 30(5):417-24. PubMed ID: 18806481
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. Pseudohypoparathyroidism type Ib in 2015.
    Mantovani G; Elli FM
    Ann Endocrinol (Paris); 2015 May; 76(2):101-4. PubMed ID: 25910998
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Progressive osseous heteroplasia, as an isolated entity or overlapping with Albright hereditary osteodystrophy.
    Lin MH; Numbenjapon N; Germain-Lee EL; Pitukcheewanont P
    J Pediatr Endocrinol Metab; 2015 Jul; 28(7-8):911-8. PubMed ID: 25894639
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [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]  

  • 28. G protein mutations in human disease.
    Weinstein LS; Shenker A
    Clin Biochem; 1993 Oct; 26(5):333-8. PubMed ID: 8299203
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [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]  

  • 30. Albright's hereditary osteodystrophy.
    Boscherini B; Coen G; Bianchini G; Gallucci G; Ballanti P; Pasquino AM; Piccolo F; Manca Bitti ML; Spadoni GL
    Acta Paediatr Scand; 1980 May; 69(3):305-9. PubMed ID: 6246707
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Presentation and clinical progression of pseudohypoparathyroidism with multi-hormone resistance and Albright hereditary osteodystrophy: a case series.
    Gelfand IM; Eugster EA; DiMeglio LA
    J Pediatr; 2006 Dec; 149(6):877-880. PubMed ID: 17137912
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. 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]  

  • 35. 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]  

  • 36. 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]  

  • 37. Early manifestation of obesity and calcinosis cutis in infantile pseudohypoparathyroidism.
    Poomthavorn P; Zacharin M
    J Paediatr Child Health; 2006 Dec; 42(12):821-3. PubMed ID: 17096721
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Eruptive, hard cutaneous nodules in a 61-year-old woman. Osteoma cutis in a patient with Albright hereditary osteodystrophy (AHO).
    Falsey RR; Ackerman L
    JAMA Dermatol; 2013 Aug; 149(8):975-6. PubMed ID: 23804016
    [No Abstract]   [Full Text] [Related]  

  • 39. [Genetic counseling in osteodystrophy Albright syndrome. Part I. Phenotypic diagnosis and pedigree analysis].
    Morawska J; Janusz L; Wasilewska E; Sierakowski S; Midro AT
    Przegl Lek; 2010; 67(7):523-6. PubMed ID: 21387768
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

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