283 related articles for article (PubMed ID: 25509509)
1. [Recurrent European missense mutation in a Hungarian pedigree with Papillon-Lefèvre syndrome].
Vályi P; Farkas K; Tripolszki K; Sulák A; Széll M; Nagy N; Nagy K
Fogorv Sz; 2014 Sep; 107(3):87-92. PubMed ID: 25509509
[TBL] [Abstract][Full Text] [Related]
2. A novel mutation of the cathepsin C gene in Papillon-Lefèvre syndrome.
Cury VF; Costa JE; Gomez RS; Boson WL; Loures CG; De ML
J Periodontol; 2002 Mar; 73(3):307-12. PubMed ID: 11922261
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Novel CTSC mutations in a patient with Papillon-Lefèvre syndrome with recurrent pyoderma and minimal oral and palmoplantar involvement.
Castori M; Madonna S; Giannetti L; Floriddia G; Milioto M; Amato S; Castiglia D
Br J Dermatol; 2009 Apr; 160(4):881-3. PubMed ID: 18945301
[No Abstract] [Full Text] [Related]
5. Papillon-Lefèvre syndrome: mutations and polymorphisms in the cathepsin C gene.
Nakano A; Nomura K; Nakano H; Ono Y; LaForgia S; Pulkkinen L; Hashimoto I; Uitto J
J Invest Dermatol; 2001 Feb; 116(2):339-43. PubMed ID: 11180012
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Papillon-Lefèvre syndrome: report of six patients and identification of a novel mutation.
Tekin B; Yucelten D; Beleggia F; Sarig O; Sprecher E
Int J Dermatol; 2016 Aug; 55(8):898-902. PubMed ID: 27062382
[TBL] [Abstract][Full Text] [Related]
8. Papillon-Lefevre syndrome: clinical presentation and a brief review.
Dhanrajani PJ
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2009 Jul; 108(1):e1-7. PubMed ID: 19540439
[TBL] [Abstract][Full Text] [Related]
9. Protein modeling of cathepsin C mutations found in Papillon-Lefèvre syndrome.
Moghaddasian M; Arab H; Dadkhah E; Boostani H; Babak AR; Abbaszadegan MR
Gene; 2014 Mar; 538(1):182-7. PubMed ID: 24374475
[TBL] [Abstract][Full Text] [Related]
10. Novel mutations of cathepsin C gene in two Chinese patients with Papillon-Lefèvre syndrome.
Yang Y; Bai X; Liu H; Li L; Cao C; Ge L
J Dent Res; 2007 Aug; 86(8):735-8. PubMed ID: 17652201
[TBL] [Abstract][Full Text] [Related]
11. Functional Cathepsin C mutations cause different Papillon-Lefèvre syndrome phenotypes.
Noack B; Görgens H; Schacher B; Puklo M; Eickholz P; Hoffmann T; Schackert HK
J Clin Periodontol; 2008 Apr; 35(4):311-6. PubMed ID: 18294227
[TBL] [Abstract][Full Text] [Related]
12. A novel seven-base deletion of the CTSC gene identified in a Hungarian family with Papillon-Lefèvre syndrome.
Farkas K; Paschali E; Papp F; Vályi P; Széll M; Kemény L; Nagy N; Csoma Z
Arch Dermatol Res; 2013 Jul; 305(5):453-5. PubMed ID: 23397598
[TBL] [Abstract][Full Text] [Related]
13. Proxy molecular diagnosis from whole-exome sequencing reveals Papillon-Lefevre syndrome caused by a missense mutation in CTSC.
Erzurumluoglu AM; Alsaadi MM; Rodriguez S; Alotaibi TS; Guthrie PA; Lewis S; Ginwalla A; Gaunt TR; Alharbi KK; Alsaif FM; Alsaadi BM; Day IN
PLoS One; 2015; 10(3):e0121351. PubMed ID: 25799584
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Papillon-Lefèvre syndrome with homozygous nonsense mutation of cathepsin C gene presenting with late-onset periodontitis.
Ragunatha S; Ramesh M; Anupama P; Kapoor M; Bhat M
Pediatr Dermatol; 2015; 32(2):292-4. PubMed ID: 24894642
[TBL] [Abstract][Full Text] [Related]
16. Phenotypic variation and allelic heterogeneity in young patients with Papillon-Lefèvre syndrome.
Ullbro C; El-Samadi S; Boumah C; Al-Yousef N; Wakil S; Twetman S; Alfadley A; Thestrup-Pedersen K; Meyer B
Acta Derm Venereol; 2006; 86(1):3-7. PubMed ID: 16585980
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. A homozygous cathepsin C mutation associated with Haim-Munk syndrome.
Cury VF; Gomez RS; Costa JE; Friedman E; Boson W; De Marco L
Br J Dermatol; 2005 Feb; 152(2):353-6. PubMed ID: 15727652
[TBL] [Abstract][Full Text] [Related]
19. Cathepsin C gene 5'-untranslated region mutation in papillon-lefèvre syndrome.
Kosem R; Debeljak M; Repič Lampret B; Kansky A; Battelino T; Trebušak Podkrajšek K
Dermatology; 2012; 225(3):193-203. PubMed ID: 23108224
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
