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 *

136 related articles for article (PubMed ID: 34552798)

  • 1. The First Vietnamese Patient of LEOPARD Syndrome due to a
    Nguyen HT; Pham NN; Anh Vu H; Tran TNA
    Case Rep Genet; 2021; 2021():8197435. PubMed ID: 34552798
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 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: 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]  

  • 5. 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]  

  • 6. 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]  

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

  • 8. Patient with confirmed LEOPARD syndrome developing multiple melanoma.
    Colmant C; Franck D; Marot L; Matthijs G; Sznajer Y; Blomme S; Tromme I
    Dermatol Pract Concept; 2018 Jan; 8(1):59-62. PubMed ID: 29445579
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. PTPN11 mutations in LEOPARD syndrome.
    Legius E; Schrander-Stumpel C; Schollen E; Pulles-Heintzberger C; Gewillig M; Fryns JP
    J Med Genet; 2002 Aug; 39(8):571-4. PubMed ID: 12161596
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. LEOPARD Syndrome: Clinical Features and Gene Mutations.
    Martínez-Quintana E; Rodríguez-González F
    Mol Syndromol; 2012 Oct; 3(4):145-57. PubMed ID: 23239957
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. LEOPARD syndrome: you could be the first one to diagnose!
    Urs P; Konde S; Chouta N; Raj S
    J Indian Soc Pedod Prev Dent; 2015; 33(1):57-60. PubMed ID: 25572376
    [TBL] [Abstract][Full Text] [Related]  

  • 17. LEOPARD Syndrome.
    Ghosh SK; Majumdar B; Rudra O; Chakraborty S
    Dermatol Online J; 2015 Oct; 21(10):. PubMed ID: 26632807
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Leopard syndrome.
    Tong KL; Ding ZP; Chua T
    Singapore Med J; 2001 Jul; 42(7):328-31. PubMed ID: 11599630
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.