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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

162 related items for PubMed ID: 25557416

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Identification of recurrent mutations in the ARS (component B) gene encoding SLURP-1 in two families with mal de Meleda.
    Ward KM, Yerebakan O, Yilmaz E, Celebi JT.
    J Invest Dermatol; 2003 Jan; 120(1):96-8. PubMed ID: 12535203
    [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.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. 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; 94(6):707-10. PubMed ID: 24604124
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. 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]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. A novel homozygous mutation disrupting the initiation codon in the SLURP1 gene underlies mal de Meleda in a consanguineous family.
    Shah K, Nasir A, Irfanullah, Shahzad S, Khan S, Ahmad W.
    Clin Exp Dermatol; 2016 Aug; 41(6):675-679. PubMed ID: 29226984
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Compound heterozygosity for ARS component B mutations in a Dutch patient with mal de Meleda.
    Nellen RG, van Geel M, Steijlen PM, van Steensel MA.
    Br J Dermatol; 2009 Apr 01; 160(4):878-80. PubMed ID: 19120323
    [No Abstract] [Full Text] [Related]

  • 16. 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 01; 41(8):764-5. PubMed ID: 24985918
    [No Abstract] [Full Text] [Related]

  • 17. A novel mutation in the ARS (component B) gene encoding SLURP-1 in a Turkish family with mal de Meleda.
    Muslumanoglu MH, Saracoglu N, Cilingir O, Basmaci T, Urer S, Sabuncu I, Demir S, Bademci G, Artan S.
    Br J Dermatol; 2006 Aug 01; 155(2):467-9. PubMed ID: 16882192
    [No Abstract] [Full Text] [Related]

  • 18. 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 01; 168(6):1372-4. PubMed ID: 23290002
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.