155 related articles for article (PubMed ID: 25618887)
1. Tuberous sclerosis complex: multisystem hamartomas.
Naderi N; Timofte I; McCurdy MT; Reed RM
BMJ Case Rep; 2015 Jan; 2015():. PubMed ID: 25618887
[No Abstract] [Full Text] [Related]
2. Angiofibromas with multiple epidermoid cysts in tuberous sclerosis: new mutation or post-traumatic?
Zheng LQ; Huang Y; Han XC
J Cutan Pathol; 2013 May; 40(5):509-12. PubMed ID: 23418925
[TBL] [Abstract][Full Text] [Related]
3. Tuberous sclerosis complex: review based on new diagnostic criteria.
Portocarrero LKL; Quental KN; Samorano LP; Oliveira ZNP; Rivitti-Machado MCDM
An Bras Dermatol; 2018 Jun; 93(3):323-331. PubMed ID: 29924239
[TBL] [Abstract][Full Text] [Related]
4. Complete inactivation of the TSC2 gene leads to formation of hamartomas.
Au KS; Hebert AA; Roach ES; Northrup H
Am J Hum Genet; 1999 Dec; 65(6):1790-5. PubMed ID: 10577937
[No Abstract] [Full Text] [Related]
5. Pathogenesis of multifocal micronodular pneumocyte hyperplasia and lymphangioleiomyomatosis in tuberous sclerosis and association with tuberous sclerosis genes TSC1 and TSC2.
Maruyama H; Ohbayashi C; Hino O; Tsutsumi M; Konishi Y
Pathol Int; 2001 Aug; 51(8):585-94. PubMed ID: 11564212
[TBL] [Abstract][Full Text] [Related]
6. The tuberous sclerosis complex.
Crino PB; Nathanson KL; Henske EP
N Engl J Med; 2006 Sep; 355(13):1345-56. PubMed ID: 17005952
[No Abstract] [Full Text] [Related]
7. Low-level mosaicism in tuberous sclerosis complex in four unrelated patients: Comparison of clinical characteristics and diagnostic pathways.
Manzanilla-Romero HH; Weis D; Schnaiter S; Rudnik-Schöneborn S
Am J Med Genet A; 2021 Dec; 185(12):3851-3858. PubMed ID: 34328706
[TBL] [Abstract][Full Text] [Related]
8. Tuberous sclerosis in a patient from Nigeria.
Ekure EN; Addissie YA; Sokunbi OJ; Kruszka P; Muenke M; Adeyemo AA
Am J Med Genet A; 2019 Aug; 179(8):1423-1425. PubMed ID: 31140686
[TBL] [Abstract][Full Text] [Related]
9. Sun exposure causes somatic second-hit mutations and angiofibroma development in tuberous sclerosis complex.
Tyburczy ME; Wang JA; Li S; Thangapazham R; Chekaluk Y; Moss J; Kwiatkowski DJ; Darling TN
Hum Mol Genet; 2014 Apr; 23(8):2023-9. PubMed ID: 24271014
[TBL] [Abstract][Full Text] [Related]
10. TSC1 and TSC2: genes that are mutated in the human genetic disorder tuberous sclerosis.
Sampson JR
Biochem Soc Trans; 2003 Jun; 31(Pt 3):592-6. PubMed ID: 12773162
[TBL] [Abstract][Full Text] [Related]
11. Tuberous sclerosis: a syndrome of incomplete tumor suppression.
McCall T; Chin SS; Salzman KL; Fults DW
Neurosurg Focus; 2006 Jan; 20(1):E3. PubMed ID: 16459993
[TBL] [Abstract][Full Text] [Related]
12. A man with a history of skin lesions and seizures.
Griffith T; Lezama JL; Sanders S; Adelman HM
Hosp Pract (1995); 2001 Jul; 36(7):15-6. PubMed ID: 11446596
[TBL] [Abstract][Full Text] [Related]
13. Sporadic facial angiofibroma and sporadic angiomyolipoma mimicking tuberous sclerosis complex.
Klonowska K; Thiele EA; Grevelink JM; Thorner AR; Kwiatkowski DJ
J Med Genet; 2022 Sep; 59(9):920-923. PubMed ID: 34635572
[TBL] [Abstract][Full Text] [Related]
14. Periungual fibroma (Koenen tumors) as isolated sign of tuberous sclerosis complex with tuberous sclerosis complex 1 germline mutation.
Quist SR; Franke I; Sutter C; Bartram CR; Gollnick HP; Leverkus M
J Am Acad Dermatol; 2010 Jan; 62(1):159-161. PubMed ID: 20082901
[No Abstract] [Full Text] [Related]
15. Survey of somatic mutations in tuberous sclerosis complex (TSC) hamartomas suggests different genetic mechanisms for pathogenesis of TSC lesions.
Niida Y; Stemmer-Rachamimov AO; Logrip M; Tapon D; Perez R; Kwiatkowski DJ; Sims K; MacCollin M; Louis DN; Ramesh V
Am J Hum Genet; 2001 Sep; 69(3):493-503. PubMed ID: 11468687
[TBL] [Abstract][Full Text] [Related]
16. A novel TSC2 mutation in a Korean patient with tuberous sclerosis complex.
Hu HJ; Chung YJ; Yoo HW; Kim YH; Eom TH
Neurol Sci; 2014 Sep; 35(9):1487-9. PubMed ID: 24770934
[No Abstract] [Full Text] [Related]
17. Isolated and unilateral facial angiofibromas revealing a type 1 segmental postzygotic mosaicism of tuberous sclerosis complex with c.4949_4982del TSC2 mutation.
Bessis D; Malinge MC; Girard C
Br J Dermatol; 2018 Jan; 178(1):e53-e54. PubMed ID: 29315486
[No Abstract] [Full Text] [Related]
18. Tuberous sclerosis complex.
Musse L
Dermatol Nurs; 2005 Oct; 17(5):376, 380. PubMed ID: 16294945
[No Abstract] [Full Text] [Related]
19. Analysis of a Mouse Skin Model of Tuberous Sclerosis Complex.
Guo Y; Dreier JR; Cao J; Du H; Granter SR; Kwiatkowski DJ
PLoS One; 2016; 11(12):e0167384. PubMed ID: 27907099
[TBL] [Abstract][Full Text] [Related]
20. A novel de novo mutation in the TSC2 gene in a Chinese patient with tuberous sclerosis complex.
Li W; Zhou P; Zhao C; Zhang Y
J Neurogenet; 2016; 30(3-4):285-287. PubMed ID: 27776463
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
