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Journal Abstract Search

138 related items for PubMed ID: 24985918

  • 1. A Japanese case of Mal de Meleda with SLURP1 mutation.
    Sakabe J, Kabashima-Kubo R, Kubo A, Sasaki T, Tokura Y.
    J Dermatol; 2014 Aug; 41(8):764-5. PubMed ID: 24985918
    [No Abstract] [Full Text] [Related]

  • 2. Pseudodominant inheritance with the G86R mutation in the ARS gene in Mal de Meleda.
    Chao SC, Huang CY, Lai FJ, Yang MH.
    Int J Dermatol; 2006 Dec; 45(12):1456-8. PubMed ID: 17184264
    [No Abstract] [Full Text] [Related]

  • 3. Mal de Meleda in Indonesia: Mutations in the SLURP1 gene appear to be ubiquitous.
    Taylor JA, Bondavalli D, Monif M, Yap LM, Winship I.
    Australas J Dermatol; 2016 Feb; 57(1):e11-3. PubMed ID: 25557416
    [Abstract] [Full Text] [Related]

  • 4. The first Mal de Meleda case in Libya: identification of a SLURP1 mutation.
    Bchetnia M, Bozgia M, Laroussi N, Ben Brick AS, Charfeddine C, Ben Halim N, Mokni M, Boubaker MS, Abdelhak S.
    Int J Dermatol; 2015 Dec; 54(12):1426-8. PubMed ID: 24738704
    [No Abstract] [Full Text] [Related]

  • 5. Identification of novel homozygous SLURP1 mutation in a Javanese family with Mal de Meleda.
    Radiono S, Pramono ZAD, Oh GGK, Surana U, Widiyani S, Danarti R.
    Int J Dermatol; 2017 Nov; 56(11):1161-1168. PubMed ID: 29023701
    [Abstract] [Full Text] [Related]

  • 6. A novel mutation in SLURP1 in patients with mal de Meleda from the Indian subcontinent.
    Nellen RG, Claessens T, Subramaniam R, Betkerur J, Prashanth A, Steijlen PM, van Geel M.
    J Dermatol Sci; 2015 Oct; 80(1):76-8. PubMed ID: 26254200
    [No Abstract] [Full Text] [Related]

  • 7. Comment on Zhao et al. "Palmoplantar keratoderma of the Gamborg-Nielsen type is caused by mutations in the SLURP1 gene and represents a variant of Mal de Meleda".
    Nellen RG, Steijlen PM, van Geel M, van Steensel MA.
    Acta Derm Venereol; 2015 Nov; 95(8):1034-5. PubMed ID: 26139149
    [No Abstract] [Full Text] [Related]

  • 8. Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene.
    Nellen RG, Steijlen PM, Hennies HC, Fischer J, Munro CS, Jonkman MF, van Steensel MA, van Geel M.
    Br J Dermatol; 2013 Jun; 168(6):1372-4. PubMed ID: 23290002
    [No Abstract] [Full Text] [Related]

  • 9. "Nagashima-type" keratosis as a novel entity in the palmoplantar keratoderma category.
    Kabashima K, Sakabe J, Yamada Y, Tokura Y.
    Arch Dermatol; 2008 Mar; 144(3):375-9. PubMed ID: 18347294
    [Abstract] [Full Text] [Related]

  • 10. Mal de Meleda without mutations in the ARS coding sequence.
    van Steensel MA, van Geel MV, Steijlen PM.
    Eur J Dermatol; 2002 Mar; 12(2):129-32. PubMed ID: 11872406
    [Abstract] [Full Text] [Related]

  • 11. Abnormal keratinization and cutaneous inflammation in Mal de Meleda.
    Kudo M, Ishiura N, Tamura-Nakano M, Shimizu T, Kamata M, Akasaka E, Nakano H, Okuma Y, Tada Y, Okochi H, Tamaki T.
    J Dermatol; 2020 May; 47(5):554-558. PubMed ID: 32157724
    [Abstract] [Full Text] [Related]

  • 12. Identification of a novel compound heterozygous mutation and a homozygous mutation of SLURP1 in Chinese families with Mal de Meleda.
    Wang T, Tang Z, Xiao T, Ren J, He S, Liu Y, Xiao S, Wang X.
    BMC Med Genomics; 2023 Jul 01; 16(1):152. PubMed ID: 37393290
    [Abstract] [Full Text] [Related]

  • 13. Mal de Meleda with homozygous mutation p.G86R in SLURP-1.
    Jia WX, Zhang YY, Wu YD, Li WR, Cheng P, Bu WB, Li CR.
    Int J Dermatol; 2020 Jun 01; 59(6):751-754. PubMed ID: 32048728
    [No Abstract] [Full Text] [Related]

  • 14. Palmoplantar keratoderma of the Gamborg-Nielsen type is caused by mutations in the SLURP1 gene and represents a variant of Mal de Meleda.
    Zhao L, Vahlquist A, Virtanen M, Wennerstrand L, Lind LK, Lundström A, Hellström Pigg M.
    Acta Derm Venereol; 2014 Nov 01; 94(6):707-10. PubMed ID: 24604124
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