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2014 1
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2020 3
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2022 6
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2024 2

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Page 1
Cross-sectional study on autosomal recessive congenital ichthyoses: association of genotype with disease severity, phenotypic and ultrastructural features in 74 Italian patients.
Diociaiuti A, Corbeddu M, Rossi S, Pisaneschi E, Cesario C, Condorelli AG, Samela T, Giancristoforo S, Angioni A, Zambruno G, Novelli A, Alaggio R, Abeni D, El Hachem M. Diociaiuti A, et al. Among authors: condorelli ag. Dermatology. 2024 Apr 8. doi: 10.1159/000536366. Online ahead of print. Dermatology. 2024. PMID: 38588653
SARS-CoV-2 infection of thymus induces loss of function that correlates with disease severity.
Rosichini M, Bordoni V, Silvestris DA, Mariotti D, Matusali G, Cardinale A, Zambruno G, Condorelli AG, Flamini S, Genah S, Catanoso M, Del Nonno F, Trezzi M, Galletti L, De Stefanis C, Cicolani N, Petrini S, Quintarelli C, Agrati C, Locatelli F, Velardi E. Rosichini M, et al. Among authors: condorelli ag. J Allergy Clin Immunol. 2023 Apr;151(4):911-921. doi: 10.1016/j.jaci.2023.01.022. Epub 2023 Feb 8. J Allergy Clin Immunol. 2023. PMID: 36758836 Free PMC article.
Combination Treatment with Hydroxytyrosol and Vitamin E Improves NAFLD-Related Fibrosis.
Panera N, Braghini MR, Crudele A, Smeriglio A, Bianchi M, Condorelli AG, Nobili R, Conti LA, De Stefanis C, Lioci G, Gurrado F, Comparcola D, Mosca A, Sartorelli MR, Scoppola V, Svegliati-Baroni G, Trombetta D, Alisi A. Panera N, et al. Among authors: condorelli ag. Nutrients. 2022 Sep 14;14(18):3791. doi: 10.3390/nu14183791. Nutrients. 2022. PMID: 36145170 Free PMC article.
IgE Sensitization Profile in Patients with Netherton Syndrome.
Scala E, Condorelli AG, Scala A, Caprini E, Didona B, Paganelli R, Castiglia D. Scala E, et al. Among authors: condorelli ag. Int Arch Allergy Immunol. 2022;183(12):1291-1296. doi: 10.1159/000526409. Epub 2022 Sep 15. Int Arch Allergy Immunol. 2022. PMID: 36108599
RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell-cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development.
Dellambra E, Cordisco S, Delle Monache F, Bondanza S, Teson M, Nicodemi EM, Didona B, Condorelli AG, Camerino G, Castiglia D, Guerra L. Dellambra E, et al. Among authors: condorelli ag. Orphanet J Rare Dis. 2022 Jul 19;17(1):275. doi: 10.1186/s13023-022-02434-2. Orphanet J Rare Dis. 2022. PMID: 35854363 Free PMC article.
Clinical and Molecular Spectrum of Sporadic Vascular Malformations: A Single-Center Study.
Diociaiuti A, Rotunno R, Pisaneschi E, Cesario C, Carnevale C, Condorelli AG, Rollo M, Di Cecca S, Quintarelli C, Novelli A, Zambruno G, El Hachem M. Diociaiuti A, et al. Among authors: condorelli ag. Biomedicines. 2022 Jun 20;10(6):1460. doi: 10.3390/biomedicines10061460. Biomedicines. 2022. PMID: 35740480 Free PMC article.
Proteasome-mediated degradation of keratins 7, 8, 17 and 18 by mutant KLHL24 in a foetal keratinocyte model: Novel insight in congenital skin defects and fragility of epidermolysis bullosa simplex with cardiomyopathy.
Logli E, Marzuolo E, D'Agostino M, Conti LA, Lena AM, Diociaiuti A, Dellambra E, Has C, Cianfanelli V, Zambruno G, El Hachem M, Magenta A, Candi E, Condorelli AG. Logli E, et al. Among authors: condorelli ag. Hum Mol Genet. 2022 Apr 22;31(8):1308-1324. doi: 10.1093/hmg/ddab318. Hum Mol Genet. 2022. PMID: 34740256 Free PMC article.
A Novel Phenotype of Junctional Epidermolysis Bullosa with Transient Skin Fragility and Predominant Ocular Involvement Responsive to Human Amniotic Membrane Eyedrops.
Castiglia D, Fortugno P, Condorelli AG, Barresi S, De Luca N, Pizzi S, Neri I, Graziano C, Trojan D, Ponzin D, Rossi S, Zambruno G, Tartaglia M. Castiglia D, et al. Among authors: condorelli ag. Genes (Basel). 2021 May 11;12(5):716. doi: 10.3390/genes12050716. Genes (Basel). 2021. PMID: 34064633 Free PMC article.
22 results