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179 results

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Page 1
Exploring shared clinical features and successful therapeutic interventions in CARD14-associated papulosquamous eruption.
Rossel SVJ, Reich A, Baniel A, Wertheim-Tysarowska K, Frommherz LH, Nolberczak D, Lesiak A, Kwiek B, Osipowicz K, Bekkenk MW, Spruijt L, Seyger MMB, Kołt-Kamińska M, Giehl K, Nartbutt J, Vreeburg M, Steijlen PM, Sprecher E, van Geel M, Gostyński AH. Rossel SVJ, et al. Among authors: giehl k. J Eur Acad Dermatol Venereol. 2024 Nov 20. doi: 10.1111/jdv.20420. Online ahead of print. J Eur Acad Dermatol Venereol. 2024. PMID: 39564931 No abstract available.
[Only a wart?-Characteristic skin changes in CHILD syndrome].
Frommherz LH, Kuna AC, Giehl K. Frommherz LH, et al. Among authors: giehl k. Dermatologie (Heidelb). 2024 Oct;75(Suppl 1):9-11. doi: 10.1007/s00105-024-05344-5. Epub 2024 Jun 7. Dermatologie (Heidelb). 2024. PMID: 39278872 German. No abstract available.
Sharing brain imaging data in the Open Science era: how and why?
Giehl K, Mutsaerts HJ, Aarts K, Barkhof F, Caspers S, Chetelat G, Colin ME, Düzel E, Frisoni GB, Ikram MA, Jovicich J, Morbelli S, Oertel W, Paret C, Perani D, Ritter P, Segura B, Wisse LEM, De Witte E, Cappa SF, van Eimeren T. Giehl K, et al. Lancet Digit Health. 2024 Jul;6(7):e526-e535. doi: 10.1016/S2589-7500(24)00069-4. Lancet Digit Health. 2024. PMID: 38906618 Free article. Review.
Association Between Years of Education and Amyloid Burden in Patients With Subjective Cognitive Decline, MCI, and Alzheimer Disease.
Hönig M, Altomare D, Caprioglio C, Collij L, Barkhof F, Van Berckel B, Scheltens P, Farrar G, Battle MR, Theis H, Giehl K, Bischof GN, Garibotto V, Molinuevo JLL, Grau-Rivera O, Delrieu J, Payoux P, Demonet JF, Nordberg AK, Savitcheva I, Walker Z, Edison P, Stephens AW, Gismondi R, Jessen F, Buckley CJ, Gispert JD, Frisoni GB, Drzezga A; AMYPAD Consortium. Hönig M, et al. Among authors: giehl k. Neurology. 2024 Mar 26;102(6):e208053. doi: 10.1212/WNL.0000000000208053. Epub 2024 Feb 20. Neurology. 2024. PMID: 38377442 Free PMC article.
[Skin manifestations as a signpost for rare genetic diseases].
Frommherz L, Giehl K. Frommherz L, et al. Among authors: giehl k. MMW Fortschr Med. 2024 Feb;166(Suppl 1):36-38. doi: 10.1007/s15006-024-3591-2. MMW Fortschr Med. 2024. PMID: 38376681 Review. German. No abstract available.
179 results