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 *

102 related articles for article (PubMed ID: 25989441)

  • 21. Genotype‒Phenotype Correlation of TRPV3-Related Olmsted Syndrome.
    Zhong W; Hu L; Cao X; Zhao J; Zhang X; Lee M; Wang H; Zhang J; Chen Q; Feng C; Duo L; Wang X; Tang L; Lin Z; Yang Y
    J Invest Dermatol; 2021 Mar; 141(3):545-554. PubMed ID: 32795529
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Olmsted syndrome: exploration of the immunological phenotype.
    Danso-Abeam D; Zhang J; Dooley J; Staats KA; Van Eyck L; Van Brussel T; Zaman S; Hauben E; Van de Velde M; Morren MA; Renard M; Van Geet C; Schaballie H; Lambrechts D; Tao J; Franckaert D; Humblet-Baron S; Meyts I; Liston A
    Orphanet J Rare Dis; 2013 May; 8():79. PubMed ID: 23692804
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mutation L437P in the 2B domain of keratin 1 causes diffuse palmoplantar keratoderma in a Chinese pedigree.
    Liu XP; Ling J; Xiong H; Shi XL; Sun X; Pan Q; Hu ZM; Wu LQ; Liang DS; Long ZG; Dai HP; Xia JH; Xia K
    J Eur Acad Dermatol Venereol; 2009 Sep; 23(9):1079-82. PubMed ID: 19470048
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Novel mutations in desmoglein 1: focal palmoplantar keratoderma in milder phenotypes.
    Zamiri M; Wilson NJ; O'Toole EA; Smith FJD
    Br J Dermatol; 2019 Sep; 181(3):618-620. PubMed ID: 30822367
    [No Abstract]   [Full Text] [Related]  

  • 25. Olmsted syndrome with erythromelalgia caused by recessive transient receptor potential vanilloid 3 mutations.
    Duchatelet S; Guibbal L; de Veer S; Fraitag S; Nitschké P; Zarhrate M; Bodemer C; Hovnanian A
    Br J Dermatol; 2014 Sep; 171(3):675-8. PubMed ID: 24606194
    [No Abstract]   [Full Text] [Related]  

  • 26. Hereditary palmoplantar keratoderma with deafness.
    Fitzgerald DA; Verbov JL
    Br J Dermatol; 1996 May; 134(5):939-42. PubMed ID: 8736341
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel mutation in TRPV3 gene causes atypical familial Olmsted syndrome.
    Ni C; Yan M; Zhang J; Cheng R; Liang J; Deng D; Wang Z; Li M; Yao Z
    Sci Rep; 2016 Feb; 6():21815. PubMed ID: 26902751
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mutation in AQP5, encoding aquaporin 5, causes palmoplantar keratoderma Bothnia type.
    Cao X; Yin J; Wang H; Zhao J; Zhang J; Dai L; Zhang J; Jiang H; Lin Z; Yang Y
    J Invest Dermatol; 2014 Jan; 134(1):284-287. PubMed ID: 23867895
    [No Abstract]   [Full Text] [Related]  

  • 29. Mutation in TRPV3 causes painful focal plantar keratoderma.
    Peters F; Kopp J; Fischer J; Tantcheva-Poór I
    J Eur Acad Dermatol Venereol; 2020 Oct; 34(10):e620-e622. PubMed ID: 32314439
    [No Abstract]   [Full Text] [Related]  

  • 30. Isolated cases of palmoplantar keratoderma, Unna-Thost type.
    Kansky A; Stanimirović A; Basta-Juzbasic A
    Cutis; 1992 Jun; 49(6):406-8. PubMed ID: 1628506
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Palmoplantar keratoderma Bothnia type with acrokeratoelastoidosis-like features due to AQP5 mutations.
    Pan Y; Men Y; Lin Z
    Clin Exp Dermatol; 2019 Jan; 44(1):88-91. PubMed ID: 30221495
    [No Abstract]   [Full Text] [Related]  

  • 32. [RHBDF2 mutations in familial palmoplantar keratoderma associated with tylosis oesophageal cancer].
    Dereure O
    Ann Dermatol Venereol; 2012; 139(8-9):605-6. PubMed ID: 22963978
    [No Abstract]   [Full Text] [Related]  

  • 33. Olmsted syndrome: clinical, molecular and therapeutic aspects.
    Duchatelet S; Hovnanian A
    Orphanet J Rare Dis; 2015 Mar; 10():33. PubMed ID: 25886873
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Transgrediens et progrediens palmoplantar keratoderma (Greither's disease) with particular histopathologic findings.
    Grilli R; Aguilar A; Escalonilla P; Soriano L; Fariña C; Martín L; Requena L
    Cutis; 2000 Mar; 65(3):141-5. PubMed ID: 10738633
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Understanding the phenotypic similarities between IFAP and Olmsted syndrome from a molecular perspective: the interaction of MBTPS2 and TRPV3.
    Nemer G; Safi R; Kreidieh F; Usta J; Bergqvist C; Ballout F; Btadini W; Hamzeh N; Abbas O; Kibbi AG; Shimomura Y; Kurban M
    Arch Dermatol Res; 2017 Oct; 309(8):637-643. PubMed ID: 28717930
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Tylosis oesophageal cancer mapped.
    Risk JM; Field EA; Field JK; Whittaker J; Fryer A; Ellis A; Shaw JM; Friedmann PS; Bishop DT; Bodmer J
    Nat Genet; 1994 Dec; 8(4):319-21. PubMed ID: 7534553
    [No Abstract]   [Full Text] [Related]  

  • 37. Japanese case of Bothnian-type palmoplantar keratoderma with a novel missense mutation of p.Trp35Ser in extracellular loop A of aquaporin-5.
    Wada Y; Kusakabe M; Nagai M; Imai Y; Yamanishi K
    J Dermatol; 2019 Mar; 46(3):e104-e106. PubMed ID: 30144154
    [No Abstract]   [Full Text] [Related]  

  • 38. [Mapping of the dominant gene of hyperkeratosis palmaris et plantaris in man].
    Rogaev EI; Korovaĭtseva GI; Ginter EK; Prytkov AN; Maksudova KhA
    Genetika; 1993 Jul; 29(7):1180-5. PubMed ID: 8370514
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Olmsted syndrome. Successful therapy by treatment with etretinate].
    Hausser I; Frantzmann Y; Anton-Lamprecht I; Estes S; Frosch PJ
    Hautarzt; 1993 Jun; 44(6):394-400. PubMed ID: 8335464
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A spontaneous KRT16 mutation in a dog breed: a model for human focal non-epidermolytic palmoplantar keratoderma (FNEPPK).
    Plassais J; Guaguère E; Lagoutte L; Guillory AS; de Citres CD; Degorce-Rubiales F; Delverdier M; Vaysse A; Quignon P; Bleuart C; Hitte C; Fautrel A; Kaerle C; Bellaud P; Bensignor E; Queney G; Bourrat E; Thomas A; André C
    J Invest Dermatol; 2015 Apr; 135(4):1187-1190. PubMed ID: 25521457
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.