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1985 2
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2000 1
2002 6
2003 1
2004 1
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2007 4
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112 results

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Page 1
Dupilumab: A Review of Present Indications and Off-Label Uses.
Muñoz-Bellido FJ, Moreno E, Dávila I. Muñoz-Bellido FJ, et al. J Investig Allergol Clin Immunol. 2022 Apr 19;32(2):97-115. doi: 10.18176/jiaci.0682. Epub 2021 Mar 3. J Investig Allergol Clin Immunol. 2022. PMID: 33661102 Free article. Review.
New possible indications are increasingly explored and include skin diseases, such as prurigo nodularis, nummular eczema, allergic contact dermatitis, chronic hand eczema, spontaneous chronic urticaria, bullous pemphigoid, alopecia areata, and Netherton syndrome, as …
New possible indications are increasingly explored and include skin diseases, such as prurigo nodularis, nummular eczema, allergic contact d …
Netherton Syndrome: Case Report and Review of the Literature.
Herz-Ruelas ME, Chavez-Alvarez S, Garza-Chapa JI, Ocampo-Candiani J, Cab-Morales VA, Kubelis-López DE. Herz-Ruelas ME, et al. Skin Appendage Disord. 2021 Aug;7(5):346-350. doi: 10.1159/000514699. Epub 2021 Jun 15. Skin Appendage Disord. 2021. PMID: 34604321 Free PMC article. Review.
Netherton syndrome (NS) is a rare genodermatosis with an autosomal recessive pattern of inheritance caused by pathogenic variants in the SPINK5 gene. ...
Netherton syndrome (NS) is a rare genodermatosis with an autosomal recessive pattern of inheritance caused by pathogenic varia …
Hyper IgE syndromes: clinical and molecular characteristics.
Al-Shaikhly T, Ochs HD. Al-Shaikhly T, et al. Immunol Cell Biol. 2019 Apr;97(4):368-379. doi: 10.1111/imcb.12209. Epub 2018 Nov 19. Immunol Cell Biol. 2019. PMID: 30264496 Review.
Hyper IgE syndromes comprise a group of rare primary immunodeficiency disorders characterized by a triad of atopic dermatitis, recurrent skin and lung infections along with elevated IgE levels. Job syndrome or autosomal dominant hyper IgE syndrome because of heteroz …
Hyper IgE syndromes comprise a group of rare primary immunodeficiency disorders characterized by a triad of atopic dermatitis, recurrent ski …
Dupilumab in Inflammatory Skin Diseases: A Systematic Review.
Olbrich H, Sadik CD, Ludwig RJ, Thaçi D, Boch K. Olbrich H, et al. Biomolecules. 2023 Mar 31;13(4):634. doi: 10.3390/biom13040634. Biomolecules. 2023. PMID: 37189381 Free PMC article. Review.
Given its relatively good safety profile, effective off-label use of dupilumab has been reported for a multitude of dermatologic diseases and several clinical trials for dermatologic skin conditions are currently ongoing. We conducted a systematic review of applications of …
Given its relatively good safety profile, effective off-label use of dupilumab has been reported for a multitude of dermatologic diseases an …
New developments in the molecular treatment of ichthyosis: review of the literature.
Joosten MDW, Clabbers JMK, Jonca N, Mazereeuw-Hautier J, Gostyński AH. Joosten MDW, et al. Orphanet J Rare Dis. 2022 Jul 15;17(1):269. doi: 10.1186/s13023-022-02430-6. Orphanet J Rare Dis. 2022. PMID: 35840979 Free PMC article. Review.
Furthermore, a lot of case series report that biological therapeutics are effective treatment options, mainly for Netherton syndrome and autosomal recessive congenital ichthyosis. It is expected that some of these new therapies will prove their efficacy and will be …
Furthermore, a lot of case series report that biological therapeutics are effective treatment options, mainly for Netherton syndro …
Topical tacrolimus for atopic dermatitis.
Cury Martins J, Martins C, Aoki V, Gois AF, Ishii HA, da Silva EM. Cury Martins J, et al. Cochrane Database Syst Rev. 2015 Jul 1;2015(7):CD009864. doi: 10.1002/14651858.CD009864.pub2. Cochrane Database Syst Rev. 2015. PMID: 26132597 Free PMC article. Review.
Exception is made for diseases with severe barrier defects, such as Netherton's syndrome, lamellar ichthyosis, and a few others, with case reports of a higher absorption. ...The reliability and strength of the evidence was limited by the lack of data; thus, findings …
Exception is made for diseases with severe barrier defects, such as Netherton's syndrome, lamellar ichthyosis, and a few other …
Biological treatments for pediatric Netherton syndrome.
Pontone M, Giovannini M, Filippeschi C, Oranges T, Pedaci FA, Mori F, Barni S, Barbati F, Consonni F, Indolfi G, Lodi L, Azzari C, Ricci S, Hovnanian A. Pontone M, et al. Front Pediatr. 2022 Dec 23;10:1074243. doi: 10.3389/fped.2022.1074243. eCollection 2022. Front Pediatr. 2022. PMID: 36619513 Free PMC article. Review.
Netherton syndrome (NS) is a rare and potentially life-threatening genetic skin disease responsible for skin inflammation and scaling, hair abnormalities and severe allergic manifestations. ...
Netherton syndrome (NS) is a rare and potentially life-threatening genetic skin disease responsible for skin inflammation and …
Dupilumab in the treatment of genodermatosis: A systematic review.
Wu PC, Dai YX, Li CL, Chen CC, Chang YT, Ma SH. Wu PC, et al. J Dtsch Dermatol Ges. 2023 Jan;21(1):7-17. doi: 10.1111/ddg.14924. Epub 2023 Jan 19. J Dtsch Dermatol Ges. 2023. PMID: 36657040 Review.
Dupilumab interferes with the signaling pathways of IL-4 and IL-13 and is effective in treating atopic dermatitis. Specific genodermatoses, including Netherton syndrome, epidermolysis bullosa pruriginosa, and hyper-IgE syndrome, are Th2 skewed diseases with a …
Dupilumab interferes with the signaling pathways of IL-4 and IL-13 and is effective in treating atopic dermatitis. Specific genodermatoses, …
Netherton Syndrome: A Genotype-Phenotype Review.
Sarri CA, Roussaki-Schulze A, Vasilopoulos Y, Zafiriou E, Patsatsi A, Stamatis C, Gidarokosta P, Sotiriadis D, Sarafidou T, Mamuris Z. Sarri CA, et al. Mol Diagn Ther. 2017 Apr;21(2):137-152. doi: 10.1007/s40291-016-0243-y. Mol Diagn Ther. 2017. PMID: 27905021 Review.
Netherton syndrome (OMIM #256500) is a rare but severe autosomal recessive form of ichthyosis that affects the skin, hair, and immune system. The identification of SPINK5, which encodes for the serine protease inhibitor LEKTI, as the gene responsible for Netherto …
Netherton syndrome (OMIM #256500) is a rare but severe autosomal recessive form of ichthyosis that affects the skin, hair, and …
Neonatal erythroderma.
Fraitag S, Bodemer C. Fraitag S, et al. Curr Opin Pediatr. 2010 Aug;22(4):438-44. doi: 10.1097/MOP.0b013e32833bc396. Curr Opin Pediatr. 2010. PMID: 20616730 Review.
PURPOSE OF REVIEW: Neonatal erythroderma is a potentially life-threatening condition in neonates less than 1 month old. ...RECENT FINDINGS: Severe erythroderma, typified by early onset, skin induration, severe alopecia and failure to thrive, is immediately suggestive of im …
PURPOSE OF REVIEW: Neonatal erythroderma is a potentially life-threatening condition in neonates less than 1 month old. ...RECENT FIN …
112 results