134 related articles for article (PubMed ID: 21387769)
1. [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]
2. 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]
3. 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]
4. [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]
5. 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]
6. 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]
7. 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]
8. 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]
9. [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]
10. 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]
11. 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]
12. 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]
13. Determination of Gs alpha protein activity in Albright's hereditary osteodystrophy.
Ahrens W; Hiort O
J Pediatr Endocrinol Metab; 2006 May; 19 Suppl 2():647-51. PubMed ID: 16789630
[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. 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]
16. GNAS1 lesions in pseudohypoparathyroidism Ia and Ic: genotype phenotype relationship and evidence of the maternal transmission of the hormonal resistance.
Linglart A; Carel JC; Garabédian M; Lé T; Mallet E; Kottler ML
J Clin Endocrinol Metab; 2002 Jan; 87(1):189-97. PubMed ID: 11788646
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
