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 *

180 related articles for article (PubMed ID: 17220626)

  • 21. Papillon-Lefèvre syndrome.
    Hickory JE; Schell J; Richard GE
    J Oral Surg; 1975 Sep; 33(9):671-2. PubMed ID: 125316
    [No Abstract]   [Full Text] [Related]  

  • 22. Papillon-Lefevre syndrome: Report of two cases in the same family.
    Nagaveni NB; Suma R; Shashikiran ND; Subba Reddy VV
    J Indian Soc Pedod Prev Dent; 2008 Jun; 26(2):78-81. PubMed ID: 18603734
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome.
    Hart TC; Hart PS; Bowden DW; Michalec MD; Callison SA; Walker SJ; Zhang Y; Firatli E
    J Med Genet; 1999 Dec; 36(12):881-7. PubMed ID: 10593994
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A genetic study of cathepsin C gene in two families with Papillon-Lefèvre syndrome.
    Allende LM; Moreno A; de Unamuno P
    Mol Genet Metab; 2003 Jun; 79(2):146-8. PubMed ID: 12809647
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Oro-dental characteristics of three siblings with Papillon-Lefevre syndrome.
    Gungor OE; Karayilmaz H; Yalcin H; Hatipoğlu M
    Niger J Clin Pract; 2017 Feb; 20(2):256-260. PubMed ID: 28091448
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Papillon-Lefèvre syndrome with albinism: a review of the literature and report of 2 brothers.
    Hattab FN; Amin WM
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2005 Dec; 100(6):709-16. PubMed ID: 16301152
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Papillon Lefevre syndrome.
    Thomas S; Gummadapu S; Ahsan A; Pai KM
    Saudi Med J; 2004 Jul; 25(7):941-3. PubMed ID: 15235704
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Papillon-Lefevre syndrome: report of two brothers.
    Vassilopoulou A; Laskaris G
    ASDC J Dent Child; 1989; 56(5):388-91. PubMed ID: 2527879
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin C.
    Hart TC; Hart PS; Michalec MD; Zhang Y; Firatli E; Van Dyke TE; Stabholz A; Zlotogorski A; Shapira L; Soskolne WA
    J Med Genet; 2000 Feb; 37(2):88-94. PubMed ID: 10662807
    [TBL] [Abstract][Full Text] [Related]  

  • 30. CTSC compound heterozygous mutations in two Chinese patients with Papillon-Lefèvre syndrome.
    Wu Y; Zhao L; Xu C; Wu Y
    Oral Dis; 2019 Jul; 25(5):1394-1402. PubMed ID: 30908832
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Successful periodontal maintenance of a case with Papillon-Lefèvre syndrome: 12-year follow-up and review of the literature.
    Wiebe CB; Häkkinen L; Putnins EE; Walsh P; Larjava HS
    J Periodontol; 2001 Jun; 72(6):824-30. PubMed ID: 11453246
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Novel cathepsin C mutation in a Brazilian family with Papillon-Lefèvre syndrome: case report and mutation update.
    Pallos D; Acevedo AC; Mestrinho HD; Cordeiro I; Hart TC
    J Dent Child (Chic); 2010; 77(1):36-41. PubMed ID: 20359428
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis.
    Toomes C; James J; Wood AJ; Wu CL; McCormick D; Lench N; Hewitt C; Moynihan L; Roberts E; Woods CG; Markham A; Wong M; Widmer R; Ghaffar KA; Pemberton M; Hussein IR; Temtamy SA; Davies R; Read AP; Sloan P; Dixon MJ; Thakker NS
    Nat Genet; 1999 Dec; 23(4):421-4. PubMed ID: 10581027
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The role of cathepsin C in Papillon-Lefèvre syndrome, prepubertal periodontitis, and aggressive periodontitis.
    Hewitt C; McCormick D; Linden G; Turk D; Stern I; Wallace I; Southern L; Zhang L; Howard R; Bullon P; Wong M; Widmer R; Gaffar KA; Awawdeh L; Briggs J; Yaghmai R; Jabs EW; Hoeger P; Bleck O; Rüdiger SG; Petersilka G; Battino M; Brett P; Hattab F; Al-Hamed M; Sloan P; Toomes C; Dixon M; James J; Read AP; Thakker N
    Hum Mutat; 2004 Mar; 23(3):222-8. PubMed ID: 14974080
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel mutation in the cathepsin C gene in a Pakistani family with Papillon-Lefevre syndrome.
    Kurban M; Cheng T; Wajid M; Kiuru M; Shimomura Y; Christiano AM
    J Eur Acad Dermatol Venereol; 2010 Aug; 24(8):967-9. PubMed ID: 20236208
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Eponym: Papillon-Lefevre syndrome.
    Dalgıc B; Bukulmez A; Sarı S
    Eur J Pediatr; 2011 Jun; 170(6):689-91. PubMed ID: 21165749
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Aggressive periodontitis associated with Papillon-Lefèvre syndrome: report of a 14-year follow-up.
    de Freitas AC; Assed S; da Silva LA; Silva RA
    Spec Care Dentist; 2007; 27(3):95-100. PubMed ID: 17658183
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Novel point mutations, deletions, and polymorphisms in the cathepsin C gene in nine families from Europe and North Africa with Papillon-Lefèvre syndrome.
    Lefèvre C; Blanchet-Bardon C; Jobard F; Bouadjar B; Stalder JF; Cure S; Hoffmann A; Prud'Homme JF; Fischer J
    J Invest Dermatol; 2001 Dec; 117(6):1657-61. PubMed ID: 11886537
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Haim Munk syndrome and Papillon Lefevre syndrome--allelic mutations in cathepsin C with variation in phenotype.
    Rai R; Thiagarajan S; Mohandas S; Natarajan K; Shanmuga Sekar C; Ramalingam S
    Int J Dermatol; 2010 May; 49(5):541-3. PubMed ID: 20534088
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Description of two new cathepsin C gene mutations in patients with Papillon-Lefèvre syndrome.
    Wani AA; Devkar N; Patole MS; Shouche YS
    J Periodontol; 2006 Feb; 77(2):233-7. PubMed ID: 16460249
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.