These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 38976110)

  • 1. Atypical left-ventricular hypertrophy with apical aneurysm in leopard syndrome.
    Fernandez-Sanchez JA; Cobarro-Galvez L; Bermudez-Jimenez FJ; Macias-Ruiz R; Oyonarte-Ramirez JM; Jimenez-Jaimez J
    Int J Cardiovasc Imaging; 2024 Jul; ():. PubMed ID: 38976110
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Case report: Distinctive cardiac features and phenotypic characteristics of Noonan syndrome with multiple lentigines among three generations in one family.
    Chan CH; Chu MF; Lam UP; Mok TM; Tam WC; Tomlinson B; Coelho R; Évora M
    Front Cardiovasc Med; 2023; 10():1225667. PubMed ID: 37692036
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Low-dose Dasatinib Ameliorates Hypertrophic Cardiomyopathy in Noonan Syndrome with Multiple Lentigines.
    Yi JS; Perla S; Huang Y; Mizuno K; Giordano FJ; Vinks AA; Bennett AM
    Cardiovasc Drugs Ther; 2022 Aug; 36(4):589-604. PubMed ID: 33689087
    [TBL] [Abstract][Full Text] [Related]  

  • 4. In vivo efficacy of the AKT inhibitor ARQ 092 in Noonan Syndrome with multiple lentigines-associated hypertrophic cardiomyopathy.
    Wang J; Chandrasekhar V; Abbadessa G; Yu Y; Schwartz B; Kontaridis MI
    PLoS One; 2017; 12(6):e0178905. PubMed ID: 28582432
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A standard echocardiographic and tissue Doppler study of morphological and functional findings in children with hypertrophic cardiomyopathy compared to those with left ventricular hypertrophy in the setting of Noonan and LEOPARD syndromes.
    Cerrato F; Pacileo G; Limongelli G; Gagliardi MG; Santoro G; Digilio MC; Di Salvo G; Ardorisio R; Miele T; Calabrò R
    Cardiol Young; 2008 Dec; 18(6):575-80. PubMed ID: 18842161
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rapidly progressive hypertrophic cardiomyopathy in an infant with Noonan syndrome with multiple lentigines: palliative treatment with a rapamycin analog.
    Hahn A; Lauriol J; Thul J; Behnke-Hall K; Logeswaran T; Schänzer A; Böğürcü N; Garvalov BK; Zenker M; Gelb BD; von Gerlach S; Kandolf R; Kontaridis MI; Schranz D
    Am J Med Genet A; 2015 Apr; 167A(4):744-51. PubMed ID: 25708222
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Heterozygous deletion of AKT1 rescues cardiac contractility, but not hypertrophy, in a mouse model of Noonan Syndrome with Multiple Lentigines.
    Roy R; Krenz M
    J Mol Cell Cardiol; 2017 Nov; 112():83-90. PubMed ID: 28911943
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Tyrosyl phosphorylation of PZR promotes hypertrophic cardiomyopathy in PTPN11-associated Noonan syndrome with multiple lentigines.
    Yi JS; Perla S; Enyenihi L; Bennett AM
    JCI Insight; 2020 Aug; 5(15):. PubMed ID: 32584792
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hypertrophic cardiomyopathy in an adult patient with Noonan syndrome with multiple lentigines.
    Rivero-García P; Campuzano-Estrada IDC; Hernandez-Felix JH
    Clin Case Rep; 2023 Jun; 11(6):e7607. PubMed ID: 37361648
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genotype-phenotype association by echocardiography offers incremental value in patients with Noonan Syndrome with Multiple Lentigines.
    Kauffman H; Ahrens-Nicklas RC; Calderon-Anyosa RJC; Ritter AL; Lin KY; Rossano JW; Quartermain MD; Banerjee A
    Pediatr Res; 2021 Aug; 90(2):444-451. PubMed ID: 33318624
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel heterozygous MAP2K1 mutation in a patient with Noonan syndrome with multiple lentigines.
    Nishi E; Mizuno S; Nanjo Y; Niihori T; Fukushima Y; Matsubara Y; Aoki Y; Kosho T
    Am J Med Genet A; 2015 Feb; 167A(2):407-11. PubMed ID: 25423878
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Multimodality Imaging of LEOPARD Syndrome: Myocardial Hypertrophy With Diffuse Coronary Artery Dilation.
    Yang D; Wang Y; Lu M
    JACC Case Rep; 2022 Aug; 4(16):1042-1048. PubMed ID: 36062059
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Importance of cardiovascular examination in patients with multiple lentigines: two cases of LEOPARD syndrome with hypertrophic cardiomyopathy.
    Jurko T; Jurko A; Krsiakova J; Jurko A; Minarik M; Mestanik M
    Acta Clin Belg; 2019 Apr; 74(2):82-85. PubMed ID: 29717636
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Natural History of Hypertrophic Cardiomyopathy in Noonan Syndrome With Multiple Lentigines.
    Monda E; Prosnitz A; Aiello R; Lioncino M; Norrish G; Caiazza M; Drago F; Beattie M; Tartaglia M; Russo MG; Colan SD; Calcagni G; Gelb BD; Kaski JP; Roberts AE; Limongelli G
    Circ Genom Precis Med; 2023 Aug; 16(4):350-358. PubMed ID: 37199218
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Paraspinal neurofibromas and hypertrophic neuropathy in Noonan syndrome with multiple lentigines.
    Conboy E; Dhamija R; Wang M; Xie J; Dyck PJ; Bridges AG; Spinner RJ; Clayton AC; Watson RE; Messiaen L; Babovic-Vuksanovic D
    J Med Genet; 2016 Feb; 53(2):123-6. PubMed ID: 26337637
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Developmental SHP2 dysfunction underlies cardiac hypertrophy in Noonan syndrome with multiple lentigines.
    Lauriol J; Cabrera JR; Roy A; Keith K; Hough SM; Damilano F; Wang B; Segarra GC; Flessa ME; Miller LE; Das S; Bronson R; Lee KH; Kontaridis MI
    J Clin Invest; 2016 Aug; 126(8):2989-3005. PubMed ID: 27348588
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Leopard syndrome.
    Sarkozy A; Digilio MC; Dallapiccola B
    Orphanet J Rare Dis; 2008 May; 3():13. PubMed ID: 18505544
    [TBL] [Abstract][Full Text] [Related]  

  • 18. LEOPARD syndrome: a variant of Noonan syndrome strongly associated with hypertrophic cardiomyopathy.
    Carcavilla A; Santomé JL; Pinto I; Sánchez-Pozo J; Guillén-Navarro E; Martín-Frías M; Lapunzina P; Ezquieta B
    Rev Esp Cardiol (Engl Ed); 2013 May; 66(5):350-6. PubMed ID: 24775816
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial aggregation of genetically heterogeneous hypertrophic cardiomyopathy: a boy with LEOPARD syndrome due to PTPN11 mutation and his nonsyndromic father lacking PTPN11 mutations.
    Digilio MC; Pacileo G; Sarkozy A; Limongelli G; Conti E; Cerrato F; Marino B; Pizzuti A; Calabrò R; Dallapiccola B
    Birth Defects Res A Clin Mol Teratol; 2004 Feb; 70(2):95-8. PubMed ID: 14991917
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.