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Journal Abstract Search

413 related items for PubMed ID: 16877242

  • 21. [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 25; 51(6):415-9. PubMed ID: 27356475
    [Abstract] [Full Text] [Related]

  • 22. Fetal rhabdomyoma: prenatal diagnosis, clinical outcome, and incidence of associated tuberous sclerosis complex.
    Bader RS, Chitayat D, Kelly E, Ryan G, Smallhorn JF, Toi A, Hornberger LK.
    J Pediatr; 2003 Nov 25; 143(5):620-4. PubMed ID: 14615733
    [Abstract] [Full Text] [Related]

  • 23. A rare case of cardiac rhabdomyomas in a dizygotic twin pair.
    Chadha R, Johnson JA, Fruitman D, Cooper SL, Wei XC, Bernier F.
    J Obstet Gynaecol Can; 2011 Aug 25; 33(8):854-857. PubMed ID: 21846442
    [Abstract] [Full Text] [Related]

  • 24. Fetal neurosonography as accurate tool for diagnosis of brain involvement in tuberous sclerosis.
    Malinger G, Prabhu A, Maroto González A, Brusilov M, Kidron D, Amster R, Birnbaum R, Krajden Haratz K.
    Ultrasound Obstet Gynecol; 2023 Sep 25; 62(3):391-397. PubMed ID: 37021742
    [Abstract] [Full Text] [Related]

  • 25. Autopsy case of right ventricular rhabdomyoma in tuberous sclerosis complex.
    Kondo T, Niida Y, Mizuguchi M, Nagasaki Y, Ueno Y, Nishimura A.
    Leg Med (Tokyo); 2019 Feb 25; 36():37-40. PubMed ID: 30336374
    [Abstract] [Full Text] [Related]

  • 26. Prenatal diagnosis of rhabdomyomas and cerebral tuberous sclerosis by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy associated with a frameshift mutation in the TSC2 gene.
    Chen CP, Su YN, Chang TY, Liu YP, Tsai FJ, Chen MR, Hwang JK, Chen TH, Wang W.
    Taiwan J Obstet Gynecol; 2010 Sep 25; 49(3):387-9. PubMed ID: 21056333
    [No Abstract] [Full Text] [Related]

  • 27. [Diagnosis of tuberous sclerosis complex focusing on prenatal period].
    Filipová H, Procházka M, Vrtěl R.
    Ceska Gynekol; 2016 Apr 25; 81(2):147-54. PubMed ID: 27457398
    [Abstract] [Full Text] [Related]

  • 28. [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 25; 28(4):361-6. PubMed ID: 21811971
    [Abstract] [Full Text] [Related]

  • 29. [Clinical analysis of 15 pediatric patients with tuberous sclerosis complex complicated by cardiac rhabdomyomas].
    Huang GQ, Zhai QX, Yu JH, Wang C, Zhuo MQ, Wang LG.
    Zhongguo Dang Dai Er Ke Za Zhi; 2015 May 25; 17(5):477-81. PubMed ID: 26014699
    [Abstract] [Full Text] [Related]

  • 30. 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, Danish Tuberous Sclerosis Group.
    Hum Mutat; 2005 Oct 25; 26(4):374-83. PubMed ID: 16114042
    [Abstract] [Full Text] [Related]

  • 31. Fetal cardiac rhabdomyoma due to paternal mosaicism of TSC2: A case report.
    Chen L, Jiang Y, Wang J.
    Medicine (Baltimore); 2020 Aug 28; 99(35):e21949. PubMed ID: 32871942
    [Abstract] [Full Text] [Related]

  • 32. Are all prenatally diagnosed multiple cardiac rhabdomyomas a sign of tuberous sclerosis?
    Jóźwiak S, Kotulska K.
    Prenat Diagn; 2006 Sep 28; 26(9):867-9. PubMed ID: 16941504
    [No Abstract] [Full Text] [Related]

  • 33. Prenatal diagnosis of cerebral lesions in Tuberous sclerosis complex (TSC). Case report and review of the literature.
    Wortmann SB, Reimer A, Creemers JW, Mullaart RA.
    Eur J Paediatr Neurol; 2008 Mar 28; 12(2):123-6. PubMed ID: 17681840
    [Abstract] [Full Text] [Related]

  • 34. 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 28; 111(1):54-63. PubMed ID: 15595939
    [Abstract] [Full Text] [Related]

  • 35. 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 18; 7():72. PubMed ID: 16981987
    [Abstract] [Full Text] [Related]

  • 36. Pattern of TSC1 and TSC2 germline mutations in Russian patients with tuberous sclerosis.
    Suspitsin EN, Yanus GA, Dorofeeva MY, Ledashcheva TA, Nikitina NV, Buyanova GV, Saifullina EV, Sokolenko AP, Imyanitov EN.
    J Hum Genet; 2018 May 18; 63(5):597-604. PubMed ID: 29476190
    [Abstract] [Full Text] [Related]

  • 37. Analysis of both TSC1 and TSC2 for germline mutations in 126 unrelated patients with tuberous sclerosis.
    Niida Y, Lawrence-Smith N, Banwell A, Hammer E, Lewis J, Beauchamp RL, Sims K, Ramesh V, Ozelius L.
    Hum Mutat; 1999 May 18; 14(5):412-22. PubMed ID: 10533067
    [Abstract] [Full Text] [Related]

  • 38. Novel TSC1 and TSC2 gene mutations in Chinese patients with tuberous sclerosis complex.
    Yu T, He Y, Li N, Zhou Y, Wang Z, Fu Q, Wang J, Wang J.
    Clin Neurol Neurosurg; 2017 Mar 18; 154():104-108. PubMed ID: 28178598
    [Abstract] [Full Text] [Related]

  • 39. Contribution of ultrafast magnetic resonance imaging in prenatal diagnosis of sonographically undetected cerebral tuberous sclerosis associated with cardiac rhabdomyomas.
    Chen CP, Liu YP, Huang JK, Chang TY, Chen MR, Chiu NC, Wang W.
    Prenat Diagn; 2005 Jun 18; 25(6):523-4. PubMed ID: 15966047
    [No Abstract] [Full Text] [Related]

  • 40. Precise prenatal diagnosis of tuberous sclerosis by sequencing the TSC2 gene.
    Milunsky A, Shim SH, Ito M, Jaekle RK, Bassett LL, Brumund MR, Milunsky JM.
    Prenat Diagn; 2005 Jul 18; 25(7):582-5. PubMed ID: 16032769
    [Abstract] [Full Text] [Related]

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