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 *

194 related articles for article (PubMed ID: 14576640)

  • 41. 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]  

  • 42. 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]  

  • 43. A Novel Mutation of the Cathepsin C Gene in Papillon-Lefévre Syndrome.
    Cury VF; Costa JE; Gomez RS; Boson WL; Loures CG; De Marco L
    J Periodontol; 2002 Mar; 73(3):307-312. PubMed ID: 29539009
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Identification of a novel cathepsin C mutation (p.W185X) in a Brazilian kindred with Papillon-Lefèvre syndrome.
    Hart PS; Pallos D; Zhang Y; Sanchez J; Kavamura I; Brunoni D; Hart TC
    Mol Genet Metab; 2002 Jun; 76(2):145-7. PubMed ID: 12083812
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Loss-of-function mutations in cathepsin C in two families with Papillon-Lefèvre syndrome are associated with deficiency of serine proteinases in PMNs.
    de Haar SF; Jansen DC; Schoenmaker T; De Vree H; Everts V; Beertsen W
    Hum Mutat; 2004 May; 23(5):524. PubMed ID: 15108292
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Papillon-Lefèvre syndrome: A new case].
    Martinho S; Levade T; Fergelot P; Stephan JL
    Arch Pediatr; 2017 Apr; 24(4):360-362. PubMed ID: 28242153
    [TBL] [Abstract][Full Text] [Related]  

  • 47. A case of Papillon-Lefevre syndrome associated with xanthogranulomatous pyelonephritis and hepatitis.
    Mansur AT; Göktay F; Demirok N
    J Dermatol; 2006 Jan; 33(1):59-63. PubMed ID: 16469088
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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]  

  • 49. Clinical, genetic, and biochemical findings in two siblings with Papillon-Lefèvre Syndrome.
    Cagli NA; Hakki SS; Dursun R; Toy H; Gokalp A; Ryu OH; Hart PS; Hart TC
    J Periodontol; 2005 Dec; 76(12):2322-9. PubMed ID: 16332247
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Biochemical and mutational analyses of the cathepsin c gene (CTSC) in three North American families with Papillon Lefèvre syndrome.
    Zhang Y; Hart PS; Moretti AJ; Bouwsma OJ; Fisher EM; Dudlicek L; Pettenati MJ; Hart TC
    Hum Mutat; 2002 Jul; 20(1):75. PubMed ID: 12112662
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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]  

  • 52. Palmoplantar keratoderma in a 7-year-old boy.
    Castellanos-González M; Rubio González B; García Cano I; Sanz Bueno J; Petiti Hebe G; Postigo C
    Pediatr Dermatol; 2013; 30(6):749-50. PubMed ID: 24283442
    [No Abstract]   [Full Text] [Related]  

  • 53. Detection of an intragenic deletion expands the spectrum of CTSC mutations in Papillon-Lefèvre syndrome.
    Jouary T; Goizet C; Coupry I; Redonnet-Vernhet I; Levade T; Burgelin I; Toutain A; Delaporte E; Douillard C; Lacombe D; Taieb A; Arveiler B
    J Invest Dermatol; 2008 Feb; 128(2):322-5. PubMed ID: 17943190
    [TBL] [Abstract][Full Text] [Related]  

  • 54. 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]  

  • 55. 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]  

  • 56. [Novel mutations of cathepsin C gene in two Chinese patients with Papillon-Lefèvre syndrome].
    Yang Y; Bai XW; Liu HS; Cao CF; Ge LH
    Zhonghua Kou Qiang Yi Xue Za Zhi; 2006 Oct; 41(10):602-5. PubMed ID: 17129448
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. Papillon-Lefèvre syndrome and malignant melanoma.
    Cook GP
    Dermatology; 2009; 219(2):187-8. PubMed ID: 19506350
    [No Abstract]   [Full Text] [Related]  

  • 59. Partial expression of Papillon-Lefèvre Syndrome.
    Kothiwale SV; Mathur S
    Indian J Dent Res; 2008; 19(3):264-6. PubMed ID: 18797107
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Mutation analysis of the cathepsin C gene in Indian families with Papillon-Lefèvre syndrome.
    Selvaraju V; Markandaya M; Prasad PV; Sathyan P; Sethuraman G; Srivastava SC; Thakker N; Kumar A
    BMC Med Genet; 2003 Jul; 4():5. PubMed ID: 12857359
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.