447 related articles for article (PubMed ID: 19254590)
1. Prenatal molecular diagnosis of tuberous sclerosis complex.
Milunsky A; Ito M; Maher TA; Flynn M; Milunsky JM
Am J Obstet Gynecol; 2009 Mar; 200(3):321.e1-6. PubMed ID: 19254590
[TBL] [Abstract][Full Text] [Related]
2. Molecular genetic, cardiac and neurodevelopmental findings in cases of prenatally diagnosed rhabdomyoma associated with tuberous sclerosis complex.
Lee KA; Won HS; Shim JY; Lee PR; Kim A
Ultrasound Obstet Gynecol; 2013 Mar; 41(3):306-11. PubMed ID: 22791573
[TBL] [Abstract][Full Text] [Related]
3. Novel mutation in the TSC2 gene associated with prenatally diagnosed cardiac rhabdomyomas and cerebral tuberous sclerosis.
Chen CP; Su YN; Hung CC; Shih JC; Wang W
J Formos Med Assoc; 2006 Jul; 105(7):599-603. PubMed ID: 16877242
[TBL] [Abstract][Full Text] [Related]
4. Mutation and polymorphism analysis of TSC1 and TSC2 genes in Indian patients with tuberous sclerosis complex.
Ali M; Girimaji SC; Markandaya M; Shukla AK; Sacchidanand S; Kumar A
Acta Neurol Scand; 2005 Jan; 111(1):54-63. PubMed ID: 15595939
[TBL] [Abstract][Full Text] [Related]
5. [Mutation screening and prenatal diagnosis of tuberous sclerosis complex].
Li W; Zhou LH; Gao BD; Li LY; Zhong CG; Gong F; Xiao HM; Song T; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug; 28(4):361-6. PubMed ID: 21811971
[TBL] [Abstract][Full Text] [Related]
6. Antenatal screening and diagnosis of tuberous sclerosis complex by fetal echocardiography and targeted genomic sequencing.
Gu X; Han L; Chen J; Wang J; Hao X; Zhang Y; Zhang J; Ge S; He Y
Medicine (Baltimore); 2018 Apr; 97(15):e0112. PubMed ID: 29642139
[TBL] [Abstract][Full Text] [Related]
7. Analysis of 65 tuberous sclerosis complex (TSC) patients by TSC2 DGGE, TSC1/TSC2 MLPA, and TSC1 long-range PCR sequencing, and report of 28 novel mutations.
Rendtorff ND; Bjerregaard B; Frödin M; Kjaergaard S; Hove H; Skovby F; Brøndum-Nielsen K; Schwartz M;
Hum Mutat; 2005 Oct; 26(4):374-83. PubMed ID: 16114042
[TBL] [Abstract][Full Text] [Related]
8. Fetal cardiac tumor: echocardiography, clinical outcome and genetic analysis in 53 cases.
Chen J; Wang J; Sun H; Gu X; Hao X; Fu Y; Zhang Y; Liu X; Zhang H; Han L; He Y
Ultrasound Obstet Gynecol; 2019 Jul; 54(1):103-109. PubMed ID: 29877000
[TBL] [Abstract][Full Text] [Related]
9. Mutational analysis of TSC1 and TSC2 in Korean patients with tuberous sclerosis complex.
Choi JE; Chae JH; Hwang YS; Kim KJ
Brain Dev; 2006 Aug; 28(7):440-6. PubMed ID: 16554133
[TBL] [Abstract][Full Text] [Related]
10. Molecular and clinical analyses of 84 patients with tuberous sclerosis complex.
Hung CC; Su YN; Chien SC; Liou HH; Chen CC; Chen PC; Hsieh CJ; Chen CP; Lee WT; Lin WL; Lee CN
BMC Med Genet; 2006 Sep; 7():72. PubMed ID: 16981987
[TBL] [Abstract][Full Text] [Related]
11. Denaturing high-performance liquid chromatography (DHPLC)-based prenatal diagnosis for tuberous sclerosis.
Bénit P; Bonnefont JP; Kara Mostefa A; Francannet C; Munnich A; Ray PF
Prenat Diagn; 2001 Apr; 21(4):279-83. PubMed ID: 11288117
[TBL] [Abstract][Full Text] [Related]
12. Tuberous sclerosis in a 19-week fetus: immunohistochemical and molecular study of hamartin and tuberin.
Wei J; Li P; Chiriboga L; Mizuguchi M; Yee H; Miller DC; Greco MA
Pediatr Dev Pathol; 2002; 5(5):448-64. PubMed ID: 12202993
[TBL] [Abstract][Full Text] [Related]
13. Detection of TSC1/TSC2 mosaic variants in patients with cardiac rhabdomyoma and tuberous sclerosis complex by hybrid-capture next-generation sequencing.
Wang S; Sun H; Wang J; Gu X; Han L; Wu Y; Yan H; Han L; Zhang H; He Y
Mol Genet Genomic Med; 2021 Oct; 9(10):e1802. PubMed ID: 34480426
[TBL] [Abstract][Full Text] [Related]
14. Clinical and genotype studies of cardiac tumors in 154 patients with tuberous sclerosis complex.
Jóźwiak S; Kotulska K; Kasprzyk-Obara J; Domańska-Pakieła D; Tomyn-Drabik M; Roberts P; Kwiatkowski D
Pediatrics; 2006 Oct; 118(4):e1146-51. PubMed ID: 16940165
[TBL] [Abstract][Full Text] [Related]
15. Prenatal genetic diagnosis of cardiac rhabdomyoma: A single-center experience.
Zhen L; Yang YD; He Y; Pan M; Han J; Yang X; Xu LL; Li DZ
Eur J Obstet Gynecol Reprod Biol; 2020 Jun; 249():7-10. PubMed ID: 32320828
[TBL] [Abstract][Full Text] [Related]
16. Mutational analysis of the TSC1 and TSC2 genes in a diagnostic setting: genotype--phenotype correlations and comparison of diagnostic DNA techniques in Tuberous Sclerosis Complex.
Sancak O; Nellist M; Goedbloed M; Elfferich P; Wouters C; Maat-Kievit A; Zonnenberg B; Verhoef S; Halley D; van den Ouweland A
Eur J Hum Genet; 2005 Jun; 13(6):731-41. PubMed ID: 15798777
[TBL] [Abstract][Full Text] [Related]
17. [Clinical application value of echocardiography combined with genetic testing in fetal cardiac rhabdomyoma].
Liu XW; Gu XY; Hao XY; Shang JF; Han L; He YH
Zhonghua Fu Chan Ke Za Zhi; 2016 Jun; 51(6):415-9. PubMed ID: 27356475
[TBL] [Abstract][Full Text] [Related]
18. Single giant mediastinal rhabdomyoma as a sole manifestation of TSC in foetus.
Godava M; Filipova H; Dubrava L; Vrtel R; Michalkova K; Janikova M; Bakaj-Zbrozkova L; Navratil J
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub; 2017 Sep; 161(3):326-329. PubMed ID: 28659645
[TBL] [Abstract][Full Text] [Related]
19. Clinical symptoms of tuberous sclerosis complex in patients with an identical TSC2 mutation.
Rok P; Kasprzyk-Obara J; Domańska-Pakieła D; Jóźwiak S
Med Sci Monit; 2005 May; 11(5):CR230-234. PubMed ID: 15874888
[TBL] [Abstract][Full Text] [Related]
20. Mutation analysis of the TSC1 and TSC2 genes in Japanese patients with pulmonary lymphangioleiomyomatosis.
Sato T; Seyama K; Fujii H; Maruyama H; Setoguchi Y; Iwakami S; Fukuchi Y; Hino O
J Hum Genet; 2002; 47(1):20-8. PubMed ID: 11829138
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
