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Insights Image for "Treatment of severe Kaposiform Lymphangiomatosis positive for NRAS mutation by MEK-inhibition".
Chowers G, Abebe-Campino G, Golan H, Vivante A, Greenberger S, Soudack M, Barkai G, Fox-Fisher I, Li D, March M, Battig MR, Hakonarson H, Adams D, Dori Y, Dagan A. Chowers G, et al. Among authors: dagan a. Pediatr Res. 2023 Dec;94(6):2117. doi: 10.1038/s41390-023-02755-3. Epub 2023 Aug 7. Pediatr Res. 2023. PMID: 37550488 No abstract available.
Whole exome sequencing in childhood-onset lupus frequently detects single gene etiologies.
Tirosh I, Spielman S, Barel O, Ram R, Stauber T, Paret G, Rubinsthein M, Pessach IM, Gerstein M, Anikster Y, Shukrun R, Dagan A, Adler K, Pode-Shakked B, Volkov A, Perelman M, Greenberger S, Somech R, Lahav E, Majmundar AJ, Padeh S, Hildebrandt F, Vivante A. Tirosh I, et al. Among authors: dagan a. Pediatr Rheumatol Online J. 2019 Jul 30;17(1):52. doi: 10.1186/s12969-019-0349-y. Pediatr Rheumatol Online J. 2019. PMID: 31362757 Free PMC article.
Treatment of severe Kaposiform lymphangiomatosis positive for NRAS mutation by MEK inhibition.
Chowers G, Abebe-Campino G, Golan H, Vivante A, Greenberger S, Soudack M, Barkai G, Fox-Fisher I, Li D, March M, Battig MR, Hakonarson H, Adams D, Dori Y, Dagan A. Chowers G, et al. Among authors: dagan a. Pediatr Res. 2023 Dec;94(6):1911-1915. doi: 10.1038/s41390-022-01986-0. Epub 2022 Mar 4. Pediatr Res. 2023. PMID: 35246606 Free PMC article.
Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disorders.
Kagan M, Semo-Oz R, Ben Moshe Y, Atias-Varon D, Tirosh I, Stern-Zimmer M, Eliyahu A, Raas-Rothschild A, Bivas M, Shlomovitz O, Chorin O, Rock R, Tzadok M, Ben-Zeev B, Heimer G, Bolkier Y, Gruber N, Dagan A, Bar Aluma BE, Pessach IM, Rechavi G, Barel O, Pode-Shakked B, Anikster Y, Vivante A. Kagan M, et al. Among authors: dagan a. Front Genet. 2023 Jan 9;13:1018062. doi: 10.3389/fgene.2022.1018062. eCollection 2022. Front Genet. 2023. PMID: 36699461 Free PMC article.
Phenotypic and molecular characteristics of CF patients carrying the I1234V mutation.
El Bar Aluma B, Sarouk I, Senderowitz H, Cohen-Cymberknoh M, Khazanov N, Dagan A, Bezalel Y, Ashkenazi M, Keler S, Efrati O. El Bar Aluma B, et al. Among authors: dagan a. Respir Med. 2020 Aug-Sep;170:106027. doi: 10.1016/j.rmed.2020.106027. Epub 2020 Jun 3. Respir Med. 2020. PMID: 32843167 Free article.
Ivacaftor for the p.Ser549Arg (S549R) gating mutation - The Israeli experience.
Dagan A, Cohen-Cymberknoh M, Shteinberg M, Levine H, Vilozni D, Bezalel Y, Bar Aluma BE, Sarouk I, Ashkenazi M, Lavie M, Tsabari R, Blau H, Kerem E, Bentur L, Efrati O, Livnat G. Dagan A, et al. Respir Med. 2017 Oct;131:225-228. doi: 10.1016/j.rmed.2017.08.026. Epub 2017 Sep 1. Respir Med. 2017. PMID: 28947035 Free article.
229 results