BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 25544017)

  • 1. 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]  

  • 2. Leopard syndrome.
    Porciello R; Divona L; Strano S; Carbone A; Calvieri C; Giustini S
    Dermatol Online J; 2008 Mar; 14(3):7. PubMed ID: 18627709
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

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

  • 7. Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11.
    Kalidas K; Shaw AC; Crosby AH; Newbury-Ecob R; Greenhalgh L; Temple IK; Law C; Patel A; Patton MA; Jeffery S
    J Hum Genet; 2005; 50(1):21-25. PubMed ID: 15690106
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Grouping of multiple-lentigines/LEOPARD and Noonan syndromes on the PTPN11 gene.
    Digilio MC; Conti E; Sarkozy A; Mingarelli R; Dottorini T; Marino B; Pizzuti A; Dallapiccola B
    Am J Hum Genet; 2002 Aug; 71(2):389-94. PubMed ID: 12058348
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. PTPN11 mutations in LEOPARD syndrome: report of four cases in Taiwan.
    Lin IS; Wang JN; Chao SC; Wu JM; Lin SJ
    J Formos Med Assoc; 2009 Oct; 108(10):803-7. PubMed ID: 19864201
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. [PTPN11 gene mutation in LEOPARD syndrome].
    Paradisi M; Pedicelli C; Ciasulli A; Pinto F; Conti E; Sarkozy A; Angelo C
    Minerva Pediatr; 2005 Aug; 57(4):189-93. PubMed ID: 16172598
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Structural insights into Noonan/LEOPARD syndrome-related mutants of protein-tyrosine phosphatase SHP2 (PTPN11).
    Qiu W; Wang X; Romanov V; Hutchinson A; Lin A; Ruzanov M; Battaile KP; Pai EF; Neel BG; Chirgadze NY
    BMC Struct Biol; 2014 Mar; 14():10. PubMed ID: 24628801
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Identification of a PTPN11 hot spot mutation in a child with atypical LEOPARD syndrome.
    Zhang J; Shen J; Cheng R; Ni C; Liang J; Li M; Yao Z
    Mol Med Rep; 2016 Sep; 14(3):2639-43. PubMed ID: 27484170
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Leopard syndrome: a report of five cases from one family in two generations.
    Begić F; Tahirović H; Kardašević M; Kalev I; Muru K
    Eur J Pediatr; 2014 Jun; 173(6):819-22. PubMed ID: 24401936
    [TBL] [Abstract][Full Text] [Related]  

  • 19. LEOPARD syndrome: what are café noir spots?
    Rodríguez-Bujaldón A; Vazquez-Bayo C; Jimenez-Puya R; Galan-Gutierrez M; Moreno-Gimenez J; Rodriguez-Garcia A; Tercedor J; Velez-Garcia A
    Pediatr Dermatol; 2008; 25(4):444-8. PubMed ID: 18789084
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Common acute lymphoblastic leukemia in a girl with genetically confirmed LEOPARD syndrome.
    Laux D; Kratz C; Sauerbrey A
    J Pediatr Hematol Oncol; 2008 Aug; 30(8):602-4. PubMed ID: 18799937
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.