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Journal Abstract Search

196 related items for PubMed ID: 35421402

  • 1. Transcriptomic Analysis of the Major Orphan Ichthyosis Subtypes Reveals Shared Immune and Barrier Signatures.
    Kim M, Mikhaylov D, Rangel SM, Pavel AB, He H, Renert-Yuval Y, Del Duca E, Malik K, Huynh T, Ibler E, Sun M, Zhang N, Estrada Y, Krueger J, Paller AS, Guttman-Yassky E.
    J Invest Dermatol; 2022 Sep; 142(9):2363-2374.e18. PubMed ID: 35421402
    [Abstract] [Full Text] [Related]

  • 2. Ichthyosis molecular fingerprinting shows profound TH17 skewing and a unique barrier genomic signature.
    Malik K, He H, Huynh TN, Tran G, Mueller K, Doytcheva K, Renert-Yuval Y, Czarnowicki T, Magidi S, Chou M, Estrada YD, Wen HC, Peng X, Xu H, Zheng X, Krueger JG, Paller AS, Guttman-Yassky E.
    J Allergy Clin Immunol; 2019 Feb; 143(2):604-618. PubMed ID: 29803800
    [Abstract] [Full Text] [Related]

  • 3. Distinct skin microbiome community structures in congenital ichthyosis.
    Tham KC, Lefferdink R, Duan K, Lim SS, Wong XFCC, Ibler E, Wu B, Abu-Zayed H, Rangel SM, Del Duca E, Chowdhury M, Chima M, Kim HJ, Lee B, Guttman-Yassky E, Paller AS, Common JEA.
    Br J Dermatol; 2022 Oct; 187(4):557-570. PubMed ID: 35633118
    [Abstract] [Full Text] [Related]

  • 4. An IL-17-dominant immune profile is shared across the major orphan forms of ichthyosis.
    Paller AS, Renert-Yuval Y, Suprun M, Esaki H, Oliva M, Huynh TN, Ungar B, Kunjravia N, Friedland R, Peng X, Zheng X, Estrada YD, Krueger JG, Choate KA, Suárez-Fariñas M, Guttman-Yassky E.
    J Allergy Clin Immunol; 2017 Jan; 139(1):152-165. PubMed ID: 27554821
    [Abstract] [Full Text] [Related]

  • 5. Inherited ichthyosis: Non-syndromic forms.
    Takeichi T, Akiyama M.
    J Dermatol; 2016 Mar; 43(3):242-51. PubMed ID: 26945532
    [Abstract] [Full Text] [Related]

  • 6. Secukinumab responses vary across the spectrum of congenital ichthyosis in adults.
    Lefferdink R, Rangel SM, Chima M, Ibler E, Pavel AB, Kim H, Wu B, Abu-Zayed H, Wu J, Jackson K, Singer G, Choate KA, Guttman-Yassky E, Paller AS.
    Arch Dermatol Res; 2023 Mar; 315(2):305-315. PubMed ID: 35218370
    [Abstract] [Full Text] [Related]

  • 7. The Major Orphan Forms of Ichthyosis Are Characterized by Systemic T-Cell Activation and Th-17/Tc-17/Th-22/Tc-22 Polarization in Blood.
    Czarnowicki T, He H, Leonard A, Malik K, Magidi S, Rangel S, Patel K, Ramsey K, Murphrey M, Song T, Estrada Y, Wen HC, Krueger JG, Guttman-Yassky E, Paller AS.
    J Invest Dermatol; 2018 Oct; 138(10):2157-2167. PubMed ID: 29660300
    [Abstract] [Full Text] [Related]

  • 8. Transepidermal water loss in the orphan forms of ichthyosis.
    Erickson TR, Murphrey MB, Abu-Zayed H, Wu B, Ibler E, Rangel SM, Paller AS.
    Pediatr Dermatol; 2020 Jul; 37(4):771-773. PubMed ID: 32515061
    [Abstract] [Full Text] [Related]

  • 9. Understanding immune profiles in ichthyosis may lead to novel therapeutic targets.
    Akiyama M.
    J Allergy Clin Immunol; 2022 Apr; 149(4):1210-1212. PubMed ID: 35218769
    [No Abstract] [Full Text] [Related]

  • 10. [Clinical presentation and etiology of ichthyoses. Overview of the new nomenclature and classification].
    Oji V.
    Hautarzt; 2010 Oct; 61(10):891-902; quiz 903-4. PubMed ID: 20827455
    [Abstract] [Full Text] [Related]

  • 11. Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis.
    Hotz A, Oji V, Bourrat E, Jonca N, Mazereeuw-Hautier J, Betz RC, Blume-Peytavi U, Stieler K, Morice-Picard F, Schönbuchner I, Markus S, Schlipf N, Fischer J.
    Acta Derm Venereol; 2016 May; 96(4):473-8. PubMed ID: 26581228
    [Abstract] [Full Text] [Related]

  • 12. [Complex syndromes related to ichthyosis].
    Bonardeaux C, de la Brassinne M.
    Rev Med Liege; 1995 Feb; 50(2):57-62. PubMed ID: 7899746
    [No Abstract] [Full Text] [Related]

  • 13. Bullous congenital ichthyosiform erythroderma.
    BARKER LP, SACHS W.
    AMA Arch Derm Syphilol; 1953 May; 67(5):443-55. PubMed ID: 13050146
    [No Abstract] [Full Text] [Related]

  • 14. Generalized blistering and erythroderma in a young girl.
    Juay L, Oon HH.
    Pediatr Dermatol; 2022 May; 39(3):464-466. PubMed ID: 35797215
    [No Abstract] [Full Text] [Related]

  • 15. [Bullous congenital ichthyosiform erythroderma].
    JABLONSKA S, SIDI E, MELKI GR, HINCKY M.
    Bull Soc Fr Dermatol Syphiligr; 1955 May; (3):316-7. PubMed ID: 13270053
    [No Abstract] [Full Text] [Related]

  • 16. Mutational Spectrum of the ABCA12 Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital Ichthyosis.
    Hotz A, Kopp J, Bourrat E, Oji V, Süßmuth K, Komlosi K, Bouadjar B, Tantcheva-Poór I, Hellström Pigg M, Betz RC, Giehl K, Schedel F, Weibel L, Schulz S, Stölzl DV, Tadini G, Demiral E, Berggard K, Zimmer AD, Alter S, Fischer J.
    Genes (Basel); 2023 Mar 15; 14(3):. PubMed ID: 36980989
    [Abstract] [Full Text] [Related]

  • 17. Keratin genes and epidermolytic hyperkeratosis.
    Burton JL.
    Lancet; 1994 Oct 22; 344(8930):1103-4. PubMed ID: 7523811
    [No Abstract] [Full Text] [Related]

  • 18. Clinical and molecular characteristics of autosomal recessive congenital ichthyosis in Thailand.
    Supsrisunjai C, Bunnag T, Chaowalit P, Boonpuen N, Kootiratrakarn T, Wessagowit V.
    Pediatr Dermatol; 2023 Jan 22; 40(1):107-112. PubMed ID: 36262015
    [Abstract] [Full Text] [Related]

  • 19. The clinical spectrum of nonbullous congenital ichthyosiform erythroderma and lamellar ichthyosis.
    Akiyama M, Sawamura D, Shimizu H.
    Clin Exp Dermatol; 2003 May 22; 28(3):235-40. PubMed ID: 12780701
    [Abstract] [Full Text] [Related]

  • 20. Update on autosomal recessive congenital ichthyosis: mRNA analysis using hair samples is a powerful tool for genetic diagnosis.
    Sugiura K, Akiyama M.
    J Dermatol Sci; 2015 Jul 22; 79(1):4-9. PubMed ID: 25982146
    [Abstract] [Full Text] [Related]

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