BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 24635075)

  • 1. Kindler syndrome with severe mucosal involvement in childhood.
    Krishna CV; Parmar NV; Has C
    Clin Exp Dermatol; 2014 Apr; 39(3):340-3. PubMed ID: 24635075
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Kindler syndrome with severe mucosal involvement in a large Palestinian pedigree.
    El Hachem M; Diociaiuti A; Proto V; Fortugno P; Zambruno G; Castiglia D; Naim M
    Eur J Dermatol; 2015; 25(1):14-9. PubMed ID: 25515598
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel and recurrent FERMT1 gene mutations in Kindler syndrome.
    Techanukul T; Sethuraman G; Zlotogorski A; Horev L; Macarov M; Trainer A; Fong K; Lens M; Medenica L; Ramesh V; McGrath JA; Lai-Cheong JE
    Acta Derm Venereol; 2011 May; 91(3):267-70. PubMed ID: 21336475
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Kindler syndrome.
    Lai-Cheong JE; McGrath JA
    Dermatol Clin; 2010 Jan; 28(1):119-24. PubMed ID: 19945624
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel pathogenic FERMT1 variant in four families with Kindler syndrome in Argentina.
    Valinotto LE; Natale MI; Lusso SB; Cella E; Gutiérrez O; Sebastiani F; Manzur GB
    Pediatr Dermatol; 2020 Mar; 37(2):337-341. PubMed ID: 31957900
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Kindler syndrome: report of two cases.
    Mendes L; Nogueira L; Vilasboas V; Talhari C; Talhari S; Santos M
    An Bras Dermatol; 2012; 87(5):779-81. PubMed ID: 23044576
    [TBL] [Abstract][Full Text] [Related]  

  • 7. First report of the c.1676G>A homozygous variant in a family with Kindler syndrome.
    Yavuz C; Başdemirci M
    Clin Exp Dermatol; 2022 Jul; 47(7):1421-1423. PubMed ID: 35388510
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sporadic Kindler syndrome with a novel mutation.
    Almeida HL; Heckler GT; Fong K; Lai-Cheong J; McGrath J
    An Bras Dermatol; 2013; 88(6 Suppl 1):212-5. PubMed ID: 24346923
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Kindler syndrome: a focal adhesion genodermatosis.
    Lai-Cheong JE; Tanaka A; Hawche G; Emanuel P; Maari C; Taskesen M; Akdeniz S; Liu L; McGrath JA
    Br J Dermatol; 2009 Feb; 160(2):233-42. PubMed ID: 19120339
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Kindler syndrome: report of three cases in a family and a brief review.
    Yazdanfar A; Hashemi B
    Int J Dermatol; 2009 Feb; 48(2):145-9. PubMed ID: 19200189
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Kindler syndrome: extension of FERMT1 mutational spectrum and natural history.
    Has C; Castiglia D; del Rio M; Diez MG; Piccinni E; Kiritsi D; Kohlhase J; Itin P; Martin L; Fischer J; Zambruno G; Bruckner-Tuderman L
    Hum Mutat; 2011 Nov; 32(11):1204-12. PubMed ID: 21936020
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Kindler syndrome: a new mutation and new diagnostic possibilities.
    Burch JM; Fassihi H; Jones CA; Mengshol SC; Fitzpatrick JE; McGrath JA
    Arch Dermatol; 2006 May; 142(5):620-4. PubMed ID: 16702500
    [TBL] [Abstract][Full Text] [Related]  

  • 13. FERMT1 promoter mutations in patients with Kindler syndrome.
    Has C; Chmel N; Levati L; Neri I; Sonnenwald T; Pigors M; Godbole K; Dudhbhate A; Bruckner-Tuderman L; Zambruno G; Castiglia D
    Clin Genet; 2015 Sep; 88(3):248-54. PubMed ID: 25156791
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Oral manifestations in Kindler syndrome: case report and discussion of literature findings.
    Barbosa NM; Visioli F; Martins MD; Martins MA; Munerato MC
    Spec Care Dentist; 2016 Jul; 36(4):223-30. PubMed ID: 26815761
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mild clinical phenotype of Kindler syndrome associated with late diagnosis and skin cancer.
    Has C; Burger B; Volz A; Kohlhase J; Bruckner-Tuderman L; Itin P
    Dermatology; 2010; 221(4):309-12. PubMed ID: 20938162
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Induction of senescence pathways in Kindler syndrome primary keratinocytes.
    Piccinni E; Di Zenzo G; Maurelli R; Dellambra E; Teson M; Has C; Zambruno G; Castiglia D
    Br J Dermatol; 2013 May; 168(5):1019-26. PubMed ID: 23278235
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Kindler syndrome: a case report and proposal for clinical diagnostic criteria.
    Fischer IA; Kazandjieva J; Vassileva S; Dourmishev A
    Acta Dermatovenerol Alp Pannonica Adriat; 2005 Jun; 14(2):61-7. PubMed ID: 16001103
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel large deletion mutation of FERMT1 gene in a Chinese patient with Kindler syndrome.
    Gao Y; Bai JL; Liu XY; Qu YJ; Cao YY; Wang JC; Jin YW; Wang H; Song F
    J Zhejiang Univ Sci B; 2015 Nov; 16(11):957-62. PubMed ID: 26537214
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Kindler syndrome. Clinical and ultrastructural findings.
    Haber RM; Hanna WM
    Arch Dermatol; 1996 Dec; 132(12):1487-90. PubMed ID: 8961879
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Kindler Syndrome: A Multidisciplinary Management Approach.
    Torres-Iberico R; Condori-Fernández Y; Apagüeño-Ruiz C; Andia-Ticona M; Pomar-Morante R
    Actas Dermosifiliogr (Engl Ed); 2020 Nov; 111(9):775-780. PubMed ID: 32861675
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.