BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 33143682)

  • 1. Where the congenital heart disease meets the pulmonary arterial hypertension, FLNA matters: a case report and literature review.
    Deng X; Li S; Qiu Q; Jin B; Yan M; Hu Y; Wu Y; Zhou H; Zhang G; Zheng X
    BMC Pediatr; 2020 Nov; 20(1):504. PubMed ID: 33143682
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lung disease associated with filamin A gene mutation: a case report.
    Eltahir S; Ahmad KS; Al-Balawi MM; Bukhamsien H; Al-Mobaireek K; Alotaibi W; Al-Shamrani A
    J Med Case Rep; 2016 Apr; 10():97. PubMed ID: 27091362
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The Efficacy of a Genetic Analysis of the BMPR2 Gene in a Patient with Severe Pulmonary Arterial Hypertension and an Atrial Septal Defect Treated with Bilateral Lung Transplantation.
    Tatebe S; Sugimura K; Aoki T; Yamamoto S; Yaoita N; Suzuki H; Sato H; Kozu K; Konno R; Satoh K; Fukuda K; Adachi O; Saito R; Nakanishi N; Morisaki H; Oyama K; Saiki Y; Okada Y; Shimokawa H
    Intern Med; 2017 Dec; 56(23):3193-3197. PubMed ID: 29021450
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Microdeletion in Xq28 with a polymorphic inversion in a patient with FLNA-associated progressive lung disease.
    Yoshii K; Matsumoto H; Hirasawa K; Sakauchi M; Hara H; Ito S; Osawa M; Fukami M; Horikawa R; Nagata S
    Respir Investig; 2019 Jul; 57(4):395-398. PubMed ID: 30987847
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease.
    Zhu N; Welch CL; Wang J; Allen PM; Gonzaga-Jauregui C; Ma L; King AK; Krishnan U; Rosenzweig EB; Ivy DD; Austin ED; Hamid R; Pauciulo MW; Lutz KA; Nichols WC; Reid JG; Overton JD; Baras A; Dewey FE; Shen Y; Chung WK
    Genome Med; 2018 Jul; 10(1):56. PubMed ID: 30029678
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cardiovascular, Brain, and Lung Involvement in a Newborn With a Novel FLNA Mutation: A Case Report and Literature Review.
    Meliota G; Vairo U; Ficarella R; Milella L; Faienza MF; D'Amato G
    Adv Neonatal Care; 2022 Apr; 22(2):125-131. PubMed ID: 33852449
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Heterogeneous Pulmonary Phenotypes in Filamin A Mutation-Related Lung Disease.
    Shah AS; Black ED; Simon DM; Gambello MJ; Garber KB; Iannucci GJ; Riedesel EL; Kasi AS
    Pediatr Allergy Immunol Pulmonol; 2021 Mar; 34(1):7-14. PubMed ID: 33734874
    [No Abstract]   [Full Text] [Related]  

  • 8. Congenital heart disease with pulmonary artery hypertension in an Asian cohort-initial report from TACHYON (TAiwan congenital heart disease associated with pulmonarY arterial hypertension) registry.
    Chiu SN; Weng KP; Lin MC; Wang JN; Hwang BT; Dai ZK; Lin SM; Chang JS; Lin IC; Wu MH; Lu CW; Lin MT; Chen CA; Hua YC; Wu JM; Wang JK;
    Int J Cardiol; 2020 Oct; 317():49-55. PubMed ID: 32522677
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Risk factors for death and the clinical features of different subtypes of patients with pulmonary arterial hypertension related to congenital heart disease].
    Xu ZY; Li QQ; Zhang C; Zhang HS; Gu H
    Zhonghua Xin Xue Guan Bing Za Zhi; 2020 Apr; 48(4):315-322. PubMed ID: 32370483
    [No Abstract]   [Full Text] [Related]  

  • 10. Lung Transplantation for FLNA-Associated Progressive Lung Disease.
    Burrage LC; Guillerman RP; Das S; Singh S; Schady DA; Morris SA; Walkiewicz M; Schecter MG; Heinle JS; Lotze TE; Lalani SR; Mallory GB
    J Pediatr; 2017 Jul; 186():118-123.e6. PubMed ID: 28457522
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A review of filamin A mutations and associated interstitial lung disease.
    Sasaki E; Byrne AT; Phelan E; Cox DW; Reardon W
    Eur J Pediatr; 2019 Feb; 178(2):121-129. PubMed ID: 30547349
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Genetic Epidemiology of Pediatric Pulmonary Arterial Hypertension.
    Haarman MG; Kerstjens-Frederikse WS; Vissia-Kazemier TR; Breeman KTN; Timens W; Vos YJ; Roofthooft MTR; Hillege HL; Berger RMF
    J Pediatr; 2020 Oct; 225():65-73.e5. PubMed ID: 32502478
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Pediatric pulmonary hypertension and pulmonary arterial hypertension secondary to congenital heart diseases].
    Olguntürk R
    Anadolu Kardiyol Derg; 2010 Aug; 10 Suppl 1():50-6. PubMed ID: 20819767
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pediatric pulmonary hypertension in the Netherlands: epidemiology and characterization during the period 1991 to 2005.
    van Loon RL; Roofthooft MT; Hillege HL; ten Harkel AD; van Osch-Gevers M; Delhaas T; Kapusta L; Strengers JL; Rammeloo L; Clur SA; Mulder BJ; Berger RM
    Circulation; 2011 Oct; 124(16):1755-64. PubMed ID: 21947294
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Filamin A (FLNA) mutation-A newcomer to the childhood interstitial lung disease (ChILD) classification.
    Shelmerdine SC; Semple T; Wallis C; Aurora P; Moledina S; Ashworth MT; Owens CM
    Pediatr Pulmonol; 2017 Oct; 52(10):1306-1315. PubMed ID: 28898549
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Pulmonary arterial hypertension as leading manifestation of methylmalonic aciduria: clinical characteristics and gene testing in 15 cases].
    Liu XQ; Yan H; Qiu JX; Zhang CY; Qi JG; Zhang X; Xiao HJ; Yang YL; Chen YH; Du JB
    Beijing Da Xue Xue Bao Yi Xue Ban; 2017 Oct; 49(5):768-777. PubMed ID: 29045954
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A case report on filamin A gene mutation and progressive pulmonary disease in an infant: A lung tissued derived mesenchymal stem cell study.
    Calcaterra V; Avanzini MA; Mantelli M; Agolini E; Croce S; De Silvestri A; Re G; Collura M; Maltese A; Novelli A; Pelizzo G
    Medicine (Baltimore); 2018 Dec; 97(50):e13033. PubMed ID: 30557962
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Transforming growth factor-beta receptor mutations and pulmonary arterial hypertension in childhood.
    Harrison RE; Berger R; Haworth SG; Tulloh R; Mache CJ; Morrell NW; Aldred MA; Trembath RC
    Circulation; 2005 Feb; 111(4):435-41. PubMed ID: 15687131
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Congenital emphysematous lung disease associated with a novel Filamin A mutation. Case report and literature review.
    Pelizzo G; Collura M; Puglisi A; Pappalardo MP; Agolini E; Novelli A; Piccione M; Cacace C; Bussani R; Corsello G; Calcaterra V
    BMC Pediatr; 2019 Mar; 19(1):86. PubMed ID: 30922288
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetics and Genomics of Pediatric Pulmonary Arterial Hypertension.
    Welch CL; Chung WK
    Genes (Basel); 2020 Oct; 11(10):. PubMed ID: 33081265
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.