204 related articles for article (PubMed ID: 23397598)
41. The novel CTSC homozygous nonsense mutation p.Lys106X in a patient with Papillon-Lefèvre syndrome with all permanent teeth remaining at over 40 years of age.
Kobayashi T; Sugiura K; Takeichi T; Akiyama M
Br J Dermatol; 2013 Oct; 169(4):948-50. PubMed ID: 23662908
[No Abstract] [Full Text] [Related]
42. 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]
43. Palmoplantar keratoderma, oral involvement, and homozygous CTSC mutation in two brothers from Cambodia.
Wei H; Wee LWY; Born B; Seang S; Koh MJA; Yee R; Lin G; Rafi'ee K; Mey S; Tan EC
Am J Med Genet A; 2020 Feb; 182(2):296-302. PubMed ID: 31846207
[TBL] [Abstract][Full Text] [Related]
44. Novel mutations in the cathepsin C gene in patients with pre-pubertal aggressive periodontitis and Papillon-Lefèvre syndrome.
Noack B; Görgens H; Hoffmann T; Fanghänel J; Kocher T; Eickholz P; Schackert HK
J Dent Res; 2004 May; 83(5):368-70. PubMed ID: 15111626
[TBL] [Abstract][Full Text] [Related]
45. 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]
46. Two patients with Papillon-Lefèvre syndrome without periodontal involvement of the permanent dentition.
Umlauft J; Schnabl D; Blunder S; Moosbrugger-Martinz V; Kapferer-Seebacher I; Zschocke J; Schmuth M; Gruber R
J Dermatol; 2021 Apr; 48(4):537-541. PubMed ID: 33580910
[TBL] [Abstract][Full Text] [Related]
47. 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]
48. Novel Compound Heterozygous Mutations in
Wang Y; Zhang H; Feng S
Ann Dermatol; 2021 Aug; 33(4):369-372. PubMed ID: 34341640
[TBL] [Abstract][Full Text] [Related]
49. Coinheritance of two rare genodermatoses (Papillon-Lefèvre syndrome and oculocutaneous albinism type 1) in two families: a genetic study.
Hewitt C; Wu CL; Hattab FN; Amin W; Ghaffar KA; Toomes C; Sloan P; Read AP; James JA; Thakker NS
Br J Dermatol; 2004 Dec; 151(6):1261-5. PubMed ID: 15606524
[TBL] [Abstract][Full Text] [Related]
50. 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]
51. Novel compound heterozygous mutations in CTSC gene cause Papillon-Lefèvre syndrome with high serum immunoglobulin E.
Li Z; Liu J; Fang S; Zhu H; Zhang X; Cai J; Li B; Xu Y
J Dermatol Sci; 2014 Dec; 76(3):258-60. PubMed ID: 25450092
[No Abstract] [Full Text] [Related]
52. Identification of novel mutation in cathepsin C gene causing Papillon-Lefèvre Syndrome in Mexican patients.
Romero-Quintana JG; Frías-Castro LO; Arámbula-Meraz E; Aguilar-Medina M; Dueñas-Arias JE; Melchor-Soto JD; Romero-Navarro JG; Ramos-Payán R
BMC Med Genet; 2013 Jan; 14():7. PubMed ID: 23311634
[TBL] [Abstract][Full Text] [Related]
53. [Gene mutational analyses of the cathepsin C gene in families with Papillon-Lefèvre syndrome].
Yuanjiao C; Chen-Jun L
Hua Xi Kou Qiang Yi Xue Za Zhi; 2016 Aug; 34(4):346-349. PubMed ID: 28317349
[TBL] [Abstract][Full Text] [Related]
54. 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]
55. Analysis of urinary cathepsin C for diagnosing Papillon-Lefèvre syndrome.
Hamon Y; Legowska M; Fergelot P; Dallet-Choisy S; Newell L; Vanderlynden L; Kord Valeshabad A; Acrich K; Kord H; Charalampos T; Morice-Picard F; Surplice I; Zoidakis J; David K; Vlahou A; Ragunatha S; Nagy N; Farkas K; Széll M; Goizet C; Schacher B; Battino M; Al Farraj Aldosari A; Wang X; Liu Y; Marchand-Adam S; Lesner A; Kara E; Korkmaz-Icöz S; Moss C; Eickholz P; Taieb A; Kavukcu S; Jenne DE; Gauthier F; Korkmaz B
FEBS J; 2016 Feb; 283(3):498-509. PubMed ID: 26607765
[TBL] [Abstract][Full Text] [Related]
56. 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]
57. [Mutational analysis of the cathepsin C gene in a family of Han nationality with Papillon-Lefevre syndrome].
Li X; Zhang X; Zhang J; Chen Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):502-5. PubMed ID: 18841559
[TBL] [Abstract][Full Text] [Related]
58. Identification of putative genetic modifying factors that influence the development of Papillon-Lefévre or Haim-Munk syndrome phenotypes.
Pap ÉM; Farkas K; Tóth L; Fábos B; Széll M; Németh G; Nagy N
Clin Exp Dermatol; 2020 Jul; 45(5):555-559. PubMed ID: 31925812
[TBL] [Abstract][Full Text] [Related]
59. Analysis of human leukocyte antigen class II gene polymorphism in Iranian patients with Papillon-Lefevre syndrome: a family study.
Farjadian S; Lotfazar M; Ghaderi A
Iran J Immunol; 2008 Sep; 5(3):171-6. PubMed ID: 18791284
[TBL] [Abstract][Full Text] [Related]
60. Papillon-Lefévre syndrome: a highly-suspected case.
Ikeshima A
J Oral Sci; 2006 Dec; 48(4):257-60. PubMed ID: 17220626
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
