199 related articles for article (PubMed ID: 3720010)
1. The McCune-Albright syndrome: a lethal gene surviving by mosaicism.
Happle R
Clin Genet; 1986 Apr; 29(4):321-4. PubMed ID: 3720010
[TBL] [Abstract][Full Text] [Related]
2. Lethal genes surviving by mosaicism: a possible explanation for sporadic birth defects involving the skin.
Happle R
J Am Acad Dermatol; 1987 Apr; 16(4):899-906. PubMed ID: 3033033
[TBL] [Abstract][Full Text] [Related]
3. Melanotic macules following Blaschko's lines in McCune-Albright syndrome.
Rieger E; Kofler R; Borkenstein M; Schwingshandl J; Soyer HP; Kerl H
Br J Dermatol; 1994 Feb; 130(2):215-20. PubMed ID: 8123575
[TBL] [Abstract][Full Text] [Related]
4. [McCune-Albright syndrome revealed by Blaschko-linear café-au-lait spots on the back].
Jung AJ; Soskin S; Paris F; Lipsker D
Ann Dermatol Venereol; 2016 Jan; 143(1):21-6. PubMed ID: 26610360
[TBL] [Abstract][Full Text] [Related]
5. G(s)alpha mutations in fibrous dysplasia and McCune-Albright syndrome.
Weinstein LS
J Bone Miner Res; 2006 Dec; 21 Suppl 2():P120-4. PubMed ID: 17229000
[TBL] [Abstract][Full Text] [Related]
6. Activating mutations of the stimulatory G protein in the McCune-Albright syndrome.
Weinstein LS; Shenker A; Gejman PV; Merino MJ; Friedman E; Spiegel AM
N Engl J Med; 1991 Dec; 325(24):1688-95. PubMed ID: 1944469
[TBL] [Abstract][Full Text] [Related]
7. McCune-Albright syndrome: molecular genetics.
Lumbroso S; Paris F; Sultan C
J Pediatr Endocrinol Metab; 2002; 15 Suppl 3():875-82. PubMed ID: 12199345
[TBL] [Abstract][Full Text] [Related]
8. Unexpected mosaicism of R201H-GNAS1 mutant-bearing cells in the testes underlie macro-orchidism without sexual precocity in McCune-Albright syndrome.
Rey RA; Venara M; Coutant R; Trabut JB; Rouleau S; Lahlou N; Sultan C; Limal JM; Picard JY; Lumbroso S
Hum Mol Genet; 2006 Dec; 15(24):3538-43. PubMed ID: 17101633
[TBL] [Abstract][Full Text] [Related]
9. McCune-Albright syndrome with acromegaly and fibrous dysplasia associated with the GNAS gene mutation identified by sensitive PNA-clamping method.
Imanaka M; Iida K; Nishizawa H; Fukuoka H; Takeno R; Takahashi K; Kaji H; Takahashi Y; Okimura Y; Kaji H; Imanishi Y; Chihara K
Intern Med; 2007; 46(18):1577-83. PubMed ID: 17878646
[TBL] [Abstract][Full Text] [Related]
10. A highly sensitive polymerase chain reaction method detects activating mutations of the GNAS gene in peripheral blood cells in McCune-Albright syndrome or isolated fibrous dysplasia.
Lietman SA; Ding C; Levine MA
J Bone Joint Surg Am; 2005 Nov; 87(11):2489-94. PubMed ID: 16264125
[TBL] [Abstract][Full Text] [Related]
11. Is McCune-Albright syndrome overlooked in subjects with fibrous dysplasia of bone?
Hannon TS; Noonan K; Steinmetz R; Eugster EA; Levine MA; Pescovitz OH
J Pediatr; 2003 May; 142(5):532-8. PubMed ID: 12756386
[TBL] [Abstract][Full Text] [Related]
12. An activating Gs alpha mutation is present in fibrous dysplasia of bone in the McCune-Albright syndrome.
Shenker A; Weinstein LS; Sweet DE; Spiegel AM
J Clin Endocrinol Metab; 1994 Sep; 79(3):750-5. PubMed ID: 8077356
[TBL] [Abstract][Full Text] [Related]
13. McCune-Albright syndrome: clinical and molecular evidence of mosaicism in an unusual giant patient.
Tinschert S; Gerl H; Gewies A; Jung HP; Nürnberg P
Am J Med Genet; 1999 Mar; 83(2):100-8. PubMed ID: 10190480
[TBL] [Abstract][Full Text] [Related]
14. Monozygotic twins discordant for the major signs of McCune-Albright syndrome.
Endo M; Yamada Y; Matsuura N; Niikawa N
Am J Med Genet; 1991 Nov; 41(2):216-20. PubMed ID: 1838461
[TBL] [Abstract][Full Text] [Related]
15. Choosing the Best Tissue and Technique to Detect Mosaicism in Fibrous Dysplasia/McCune-Albright Syndrome (FD/MAS).
Vado Y; Manero-Azua A; Pereda A; Perez de Nanclares G
Genes (Basel); 2024 Jan; 15(1):. PubMed ID: 38255009
[No Abstract] [Full Text] [Related]
16. Reproduction of human fibrous dysplasia of bone in immunocompromised mice by transplanted mosaics of normal and Gsalpha-mutated skeletal progenitor cells.
Bianco P; Kuznetsov SA; Riminucci M; Fisher LW; Spiegel AM; Robey PG
J Clin Invest; 1998 Apr; 101(8):1737-44. PubMed ID: 9541505
[TBL] [Abstract][Full Text] [Related]
17. Primary hyperparathyroidism-associated polyostotic fibrous dysplasia: absence of McCune-Albright syndrome mutations.
Hammami MM; al-Zahrani A; Butt A; Vencer LJ; Hussain SS
J Endocrinol Invest; 1997 Oct; 20(9):552-8. PubMed ID: 9413810
[TBL] [Abstract][Full Text] [Related]
18. Fibrous dysplasia of bone and McCune-Albright syndrome.
Chapurlat RD; Orcel P
Best Pract Res Clin Rheumatol; 2008 Mar; 22(1):55-69. PubMed ID: 18328981
[TBL] [Abstract][Full Text] [Related]
19. DIAGNOSIS OF ENDOCRINE DISEASE: Mosaic disorders of FGF23 excess: Fibrous dysplasia/McCune-Albright syndrome and cutaneous skeletal hypophosphatemia syndrome.
de Castro LF; Ovejero D; Boyce AM
Eur J Endocrinol; 2020 May; 182(5):R83-R99. PubMed ID: 32069220
[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]