130 related articles for article (PubMed ID: 19329231)
1. [Subcutaneous calcifications and dysmorphic syndrome].
Avenel G; Bernet J; Lahaxe L; Lévesque H; Marie I
Rev Med Interne; 2010 Mar; 31(3):238-40. PubMed ID: 19329231
[No 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. 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]
4. [Pseudohypoparathyroidism].
Yasuda T
Nihon Rinsho; 2005 Oct; 63 Suppl 10():352-6. PubMed ID: 16279661
[No Abstract] [Full Text] [Related]
5. [McCune-Albright syndrome].
Miyoshi Y; Ozono K; Yamamoto T
Nihon Rinsho; 2005 Oct; 63 Suppl 10():534-8. PubMed ID: 16279696
[No Abstract] [Full Text] [Related]
6. Pseudohypoparathyroidism: history of the disease.
de Sanctis L
J Pediatr Endocrinol Metab; 2006 May; 19 Suppl 2():627-33. PubMed ID: 16789627
[No Abstract] [Full Text] [Related]
7. Genetic and molecular aspects of McCune-Albright syndrome.
Lietman SA; Schwindinger WF; Levine MA
Pediatr Endocrinol Rev; 2007 Aug; 4 Suppl 4():380-5. PubMed ID: 17982384
[TBL] [Abstract][Full Text] [Related]
8. Tocilizumab in the treatment of a polyostotic variant of fibrous dysplasia of bone.
de Boysson H; Johnson A; Hablani N; Hajlaoui W; Auzary C; Geffray L
Rheumatology (Oxford); 2015 Sep; 54(9):1747-9. PubMed ID: 26070936
[No Abstract] [Full Text] [Related]
9. 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]
10. 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]
11. [Albright hereditary osteodystrophy].
Tohma T
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):131-2. PubMed ID: 11057167
[No Abstract] [Full Text] [Related]
12. McCune-Albright syndrome in a discordant monozygotic twin.
Peleg R; Luba A; Eliakim A; Israeli-Shani L; Manor E; Birk R; Parvari R
Isr Med Assoc J; 2009 Jun; 11(6):343-7. PubMed ID: 19697584
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Early manifestation of calcinosis cutis in pseudohypoparathyroidism type Ia associated with a novel mutation in the GNAS gene.
Riepe FG; Ahrens W; Krone N; Fölster-Holst R; Brasch J; Sippell WG; Hiort O; Partsch CJ
Eur J Endocrinol; 2005 Apr; 152(4):515-9. PubMed ID: 15817905
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. Ovarian dysfunction by activating mutation of GS alpha: McCune-Albright syndrome as a model.
Chanson P; Salenave S; Young J
Ann Endocrinol (Paris); 2010 May; 71(3):210-3. PubMed ID: 20362972
[TBL] [Abstract][Full Text] [Related]
18. [Somatic mosaicism in genetic diseases].
Tonoki H
Nihon Rinsho; 2005 Dec; 63 Suppl 12():81-6. PubMed ID: 16416775
[No Abstract] [Full Text] [Related]
19. [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]
20. [Fibrous dysplasia of bone].
Sone T
Nihon Rinsho; 2006 Jun; Suppl 2():148-51. PubMed ID: 16817371
[No Abstract] [Full Text] [Related]
[Next] [New Search]
