BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 32866449)

  • 1. Familial LEOPARD Syndrome With Hypertrophic Cardiomyopathy.
    Galazka P; Jain R; Muthukumar L; Sanders H; Bush M; Jan MF; Jahangir A; Khandheria BK; Tajik AJ
    Am J Cardiol; 2020 Nov; 135():168-173. PubMed ID: 32866449
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

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

  • 5. 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]  

  • 6. LEOPARD syndrome and hypertrophic obstructive cardiomyopathy: a case report.
    Cetinkaya E; Günal N; Sönmez N; Aycan Z; Vidinlisan S; Kahramanyol O; Paşaoğlu I
    Turk J Pediatr; 2004; 46(4):373-6. PubMed ID: 15641276
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotypical diversity of patients with LEOPARD syndrome carrying the worldwide recurrent p.Tyr279Cys PTPN11 mutation.
    Nemes E; Farkas K; Kocsis-Deák B; Drubi A; Sulák A; Tripolszki K; Dósa P; Ferenc L; Nagy N; Széll M
    Arch Dermatol Res; 2015 Dec; 307(10):891-5. PubMed ID: 26377839
    [TBL] [Abstract][Full Text] [Related]  

  • 8. LEOPARD syndrome without hearing loss or pulmonary stenosis: a report of 2 cases.
    Ramos-Geldres TT; Dávila-Seijo P; Duat-Rodríguez A; Noguera-Morel L; Ezquieta-Zubicaray B; Rosón-López E; Hernández-Martín A; Torrelo-Fernández A
    Actas Dermosifiliogr; 2015 May; 106(4):e19-22. PubMed ID: 25544017
    [TBL] [Abstract][Full Text] [Related]  

  • 9. LEOPARD Syndrome Caused by Tyr279Cys Mutation in the PTPN11 Gene.
    Martínez-Quintana E; Rodríguez-González F
    Mol Syndromol; 2012 Apr; 2(6):251-253. PubMed ID: 22822385
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Severe, early onset hypertrophic cardiomyopathy in a family with LEOPARD syndrome.
    Limongelli G; Pacileo G; Russo MG; Sarkozy A; Felicetti M; Di Salvo G; Morelli C; Calabrò P; Paladini D; Marino B; Dallapiccola B; Calabrò R
    J Prenat Med; 2008 Apr; 2(2):24-6. PubMed ID: 22439023
    [TBL] [Abstract][Full Text] [Related]  

  • 12. LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD.
    Kim J; Kim MR; Kim HJ; Lee KA; Lee MG
    Ann Dermatol; 2011 May; 23(2):232-5. PubMed ID: 21747628
    [TBL] [Abstract][Full Text] [Related]  

  • 13. LEOPARD syndrome with recurrent PTPN11 mutation Y279C and different cutaneous manifestations: two case reports and a review of the literature.
    Kalev I; Muru K; Teek R; Zordania R; Reimand T; Köbas K; Ounap K
    Eur J Pediatr; 2010 Apr; 169(4):469-73. PubMed ID: 19768645
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Acute myelomonocytic leukemia in a boy with LEOPARD syndrome (PTPN11 gene mutation positive).
    Uçar C; Calýskan U; Martini S; Heinritz W
    J Pediatr Hematol Oncol; 2006 Mar; 28(3):123-5. PubMed ID: 16679933
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Leopard syndrome and hypertrophic cardiomyopathy: an association related to sudden death.
    Antunes Mde O; Arteaga E; Matsumoto AY; Ianni BM
    Arq Bras Cardiol; 2009 Jun; 92(6):e44-6, e71-3. PubMed ID: 19629299
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The case of 17-year-old male with LEOPARD syndrome.
    Dzemeshkevich S; Frolova J; Betekhtin M; Shapieva A; Rizun L
    J Cardiol Cases; 2013 Feb; 7(2):e37-e41. PubMed ID: 30533116
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Lessons From a Genotype-Phenotype Study About the Clinical Spectrum of Hypertrophic Cardiomyopathy Associated With Noonan Syndrome With Multiple Lentigines and PTPN11-Mutations.
    Östman-Smith I
    Circ Genom Precis Med; 2023 Aug; 16(4):359-362. PubMed ID: 37325916
    [No Abstract]   [Full Text] [Related]  

  • 18. Leopard syndrome: the potential cardiac defect underlying skin phenotypes.
    Yue X; Zhao X; Dai Y; Yu L
    Hereditas; 2021 Sep; 158(1):34. PubMed ID: 34488904
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Implantable cardioverter defibrillator for progressive hypertrophic cardiomyopathy in a patient with LEOPARD syndrome and a novel PTPN11 mutation Gln510His.
    Wakabayashi Y; Yamazaki K; Narumi Y; Fuseya S; Horigome M; Wakui K; Fukushima Y; Matsubara Y; Aoki Y; Kosho T
    Am J Med Genet A; 2011 Oct; 155A(10):2529-33. PubMed ID: 21910226
    [TBL] [Abstract][Full Text] [Related]  

  • 20. LEOPARD syndrome: clinical diagnosis in the first year of life.
    Digilio MC; Sarkozy A; de Zorzi A; Pacileo G; Limongelli G; Mingarelli R; Calabrò R; Marino B; Dallapiccola B
    Am J Med Genet A; 2006 Apr; 140(7):740-6. PubMed ID: 16523510
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.