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 *

166 related articles for article (PubMed ID: 25865288)

  • 1. A novel mutation in the FERMT1 gene in Turkish siblings with Kindler syndrome.
    Kartal D; Borlu M; Has C; Fölster-Holst R
    J Eur Acad Dermatol Venereol; 2016 Jul; 30(7):1233-5. PubMed ID: 25865288
    [No Abstract]   [Full Text] [Related]  

  • 2. Case of Kindler syndrome resulting from mutation in the FERMT1 gene.
    Wada M; Masuda K; Tsuruta D; Tamai K; Lai-Cheong JE; McGrath JA; Katoh N
    J Dermatol; 2012 Dec; 39(12):1057-8. PubMed ID: 22672060
    [No Abstract]   [Full Text] [Related]  

  • 3. The Kindler syndrome: a spectrum of FERMT1 mutations in Iranian families.
    Youssefian L; Vahidnezhad H; Barzegar M; Li Q; Sotoudeh S; Yazdanfar A; Ehsani AH; Kajbafzadeh AM; Mozafari N; Ebrahimi Daryani N; Agha-Hosseini F; Zeinali S; Uitto J
    J Invest Dermatol; 2015 May; 135(5):1447-1450. PubMed ID: 25599393
    [No Abstract]   [Full Text] [Related]  

  • 4. A Deep-Intronic FERMT1 Mutation Causes Kindler Syndrome: An Explanation for Genetically Unsolved Cases.
    Chmel N; Danescu S; Gruler A; Kiritsi D; Bruckner-Tuderman L; Kreuter A; Kohlhase J; Has C
    J Invest Dermatol; 2015 Nov; 135(11):2876-2879. PubMed ID: 26083552
    [No Abstract]   [Full Text] [Related]  

  • 5. Two novel mutations in KIND1 in Indian patients with Kindler syndrome.
    Kantheti P; Kubba A; Prabhu A; Batrani M; Hiremagalore R
    Clin Exp Dermatol; 2017 Jan; 42(1):95-97. PubMed ID: 27862150
    [No Abstract]   [Full Text] [Related]  

  • 6. Congenital bullous poikiloderma (Kindler syndrome) - new mutation.
    Lennartz L; Has C; Lehmann P
    J Dtsch Dermatol Ges; 2012 Dec; 10(12):919-20. PubMed ID: 23078512
    [No Abstract]   [Full Text] [Related]  

  • 7. What is Kindler syndrome?
    Lai-Cheong JE; McGrath JA
    Skinmed; 2011; 9(3):145-6. PubMed ID: 21675491
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Founder mutation c.676insC in three unrelated Kindler syndrome families belonging to a particular clan from Pakistan.
    Shaiq PA; Klausegger A; Muzaffar F; Bauer JW; Khan MI; Khanum A; Qamar R; Raja GK
    J Dermatol; 2012 Jul; 39(7):640-1. PubMed ID: 22220914
    [No Abstract]   [Full Text] [Related]  

  • 12. Revertant mosaicism in Kindler syndrome.
    Lai-Cheong JE; Moss C; Parsons M; Almaani N; McGrath JA
    J Invest Dermatol; 2012 Mar; 132(3 Pt 1):730-2. PubMed ID: 22089829
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. A novel mutation in the FERMT1 gene in a Spanish family with Kindler's syndrome.
    Mas-Vidal A; Miñones-Suárez L; Toral JF; Mallo S; Pérez-Oliva N
    J Eur Acad Dermatol Venereol; 2010 Aug; 24(8):978-9. PubMed ID: 20028441
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. Kindler syndrome with severe intestinal involvement: a 31-year follow-up.
    Shimizu S; Nishie W; Tsuchiya K; Inokuma D; Koguchi-Yoshioka H; Kikuchi K; Motoya S; Nakamura H; Shimizu H
    Acta Derm Venereol; 2014 May; 94(3):351-2. PubMed ID: 24002169
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. A case of Kindler syndrome in a young Indian female with exon deletion.
    Fukushi R; Tsuboi R; Maeda T; Kanda Y; Sakai N; Suzuki S; Harada K
    Int J Dermatol; 2019 Jan; 58(1):e19-e21. PubMed ID: 30414177
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.