216 related articles for article (PubMed ID: 25946540)
1. [Clinical and molecular findings of pachyonychia congenita type 2 (PC-2)].
Cammarata-Scalisi F; Natsuga K; Toyonaga E; Nishie W; Shimizu H; Stock F; Milano M; Petrosino P; Arenas de Sotolongo A; Medina Y
Gac Med Mex; 2015; 151(2):270-2. PubMed ID: 25946540
[TBL] [Abstract][Full Text] [Related]
2. First case of pachyonychia congenita in the Czech Republic.
Jiráková A; Rajská L; Rob F; Džambová M; Sečníková Z; Göpfertová D; Schwartz M; Smith F; Lotti T; Hercogová J
Dermatol Ther; 2015; 28(1):10-2. PubMed ID: 25174302
[TBL] [Abstract][Full Text] [Related]
3. A large mutational study in pachyonychia congenita.
Wilson NJ; Leachman SA; Hansen CD; McMullan AC; Milstone LM; Schwartz ME; McLean WH; Hull PR; Smith FJ
J Invest Dermatol; 2011 May; 131(5):1018-24. PubMed ID: 21326300
[TBL] [Abstract][Full Text] [Related]
4. Revisiting pachyonychia congenita: a case-cohort study of 815 patients.
Samuelov L; Smith FJD; Hansen CD; Sprecher E
Br J Dermatol; 2020 Mar; 182(3):738-746. PubMed ID: 31823354
[TBL] [Abstract][Full Text] [Related]
5. Pachyonychia congenita type 2 (Jackson-Lawler syndrome) or PC-17: case report.
Morais P; Peralta L; Loureiro M; Coelho S
Acta Dermatovenerol Croat; 2013; 21(1):48-51. PubMed ID: 23683487
[TBL] [Abstract][Full Text] [Related]
6. Pachyonychia congenita in pediatric patients: natural history, features, and impact.
Shah S; Boen M; Kenner-Bell B; Schwartz M; Rademaker A; Paller AS
JAMA Dermatol; 2014 Feb; 150(2):146-53. PubMed ID: 24132595
[TBL] [Abstract][Full Text] [Related]
7. Generalized bullae in a young girl with KRT6A-related pachyonychia congenita.
Liu J; Zhong W; Yu B; Lin Z; Zheng Y; Hu X
Pediatr Dermatol; 2020 Sep; 37(5):974-976. PubMed ID: 32662074
[TBL] [Abstract][Full Text] [Related]
8. Pachyonychia congenita: a case report.
Kohli N
Cutis; 2009 Nov; 84(5):269-71. PubMed ID: 20099620
[TBL] [Abstract][Full Text] [Related]
9. The histopathological features of the nail plate in pachyonychia congenita.
Stewart CL; Takeshita J; Hansen CD; Rubin AI
J Cutan Pathol; 2020 Apr; 47(4):357-362. PubMed ID: 31845382
[TBL] [Abstract][Full Text] [Related]
10. A case of pachyonychia congenita with unusual manifestations: an unusual type or a new syndrome?
Gönül M; Gül Ü; Kılıç A; Soylu S; Koçak O; Demiriz M
Int J Dermatol; 2015 Mar; 54(3):334-7. PubMed ID: 25713981
[TBL] [Abstract][Full Text] [Related]
11. Pachyonychia congenita: a case report of a successful treatment with rosuvastatin in a patient with a KRT6A mutation.
Abdollahimajd F; Rajabi F; Shahidi-Dadras M; Saket S; Youssefian L; Vahidnezhad H; Uitto J
Br J Dermatol; 2019 Sep; 181(3):584-586. PubMed ID: 30307612
[TBL] [Abstract][Full Text] [Related]
12. The molecular genetic analysis of the expanding pachyonychia congenita case collection.
Wilson NJ; O'Toole EA; Milstone LM; Hansen CD; Shepherd AA; Al-Asadi E; Schwartz ME; McLean WH; Sprecher E; Smith FJ
Br J Dermatol; 2014 Aug; 171(2):343-55. PubMed ID: 24611874
[TBL] [Abstract][Full Text] [Related]
13. Molecular epidemiology of pachyonychia congenita in the Israeli population.
Pavlovsky M; Peled A; Samuelov L; Malki L; Malovitski K; Assaf S; Mohamad J; Meijers O; Eskin-Schwartz M; Sarig O; Sprecher E
Clin Exp Dermatol; 2021 Jun; 46(4):663-668. PubMed ID: 33190296
[TBL] [Abstract][Full Text] [Related]
14. Phenotype and genotype features of Vietnamese children with pachyonychia congenita.
Chu HT; Dinh Duong TA; Le DH; Le TV; Nguyen BB; Dang CV; Vu QV
Pediatr Neonatol; 2023 Jul; 64(4):405-410. PubMed ID: 36658016
[TBL] [Abstract][Full Text] [Related]
15. Pachyonychia congenita patients with mutations in KRT6A have more extensive disease compared with patients who have mutations in KRT16.
Spaunhurst KM; Hogendorf AM; Smith FJ; Lingala B; Schwartz ME; Cywinska-Bernas A; Zeman KJ; Tang JY
Br J Dermatol; 2012 Apr; 166(4):875-8. PubMed ID: 22098151
[TBL] [Abstract][Full Text] [Related]
16. A novel missense mutation L468Q of keratin 6a in pachyonychia congenita type 1.
Zhou HL; Yang S; Gao M; Zhao XY; Zhu YG; Li W; Ren YQ; Liang YH; Du WH; Zhang XJ
J Eur Acad Dermatol Venereol; 2007 Mar; 21(3):351-5. PubMed ID: 17309457
[TBL] [Abstract][Full Text] [Related]
17. Pachyonychia congenita type 2, N92S mutation of keratin 17 gene: clinical features, mutation analysis and pathological view.
Cogulu O; Onay H; Aykut A; Wilson NJ; Smith FJ; Dereli T; Ozkinay F
Eur J Pediatr; 2009 Oct; 168(10):1269-72. PubMed ID: 19107515
[TBL] [Abstract][Full Text] [Related]
18. A KRT6A mutation p.Ile462Asn in a Chinese family with pachyonychia congenita, and identification of maternal mosaicism: a case report.
Li Y; Wang Y; Ming Y; Chaolan P; Jia Z; Cheng N; Qiaoyu C; Li M; Tianyi X
BMC Med Genomics; 2021 Nov; 14(1):259. PubMed ID: 34724947
[TBL] [Abstract][Full Text] [Related]
19. Pachyonychia Congenita: A Spectrum of KRT6a Mutations in Australian Patients.
Forrest CE; Casey G; Mordaunt DA; Thompson EM; Gordon L
Pediatr Dermatol; 2016 May; 33(3):337-42. PubMed ID: 27041546
[TBL] [Abstract][Full Text] [Related]
20. Keratin 17 Mutations in Four Families from India with Pachyonychia Congenita.
Agarwala M; Salphale P; Peter D; Wilson NJ; Pulimood S; Schwartz ME; Smith FJD
Indian J Dermatol; 2017; 62(4):422-426. PubMed ID: 28794556
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
