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SIGLEC1 (CD169) as a potential diagnostical screening marker for monogenic interferonopathies.
Orak B, Ngoumou G, Ebstein F, Zieba B, Goetzke CC, Knierim E, Kaindl AM, Panzer A, Theophil M, Berns M, Krüger E, Meisel C, Unterwalder N, Kallinich T. Orak B, et al. Among authors: kaindl am. Pediatr Allergy Immunol. 2021 Apr;32(3):621-625. doi: 10.1111/pai.13400. Epub 2020 Nov 9. Pediatr Allergy Immunol. 2021. PMID: 33099809 No abstract available.
Atypical NMDA receptor expression in a diffuse astrocytoma, MYB- or MYBL1-altered as a trigger for autoimmune encephalitis.
Nikolaus M, Koch A, Stenzel W, Elezkurtaj S, Sahm F, Tietze A, Stöffler L, Kreye J, Hernáiz Driever P, Thomale UW, Kaindl AM, Schuelke M, Knierim E. Nikolaus M, et al. Among authors: kaindl am. Acta Neuropathol. 2022 Aug;144(2):385-389. doi: 10.1007/s00401-022-02447-y. Epub 2022 Jun 21. Acta Neuropathol. 2022. PMID: 35727368 Free PMC article. No abstract available.
Pediatric de novo movement disorders and ataxia in the context of SARS-CoV-2.
Wilpert NM, de Almeida Marcelino AL, Knierim E, Incoronato P, Sanchez-Sendin E, Staudacher O, Drenckhahn A, Bittigau P, Kreye J, Prüss H, Schuelke M, Kühn AA, Kaindl AM, Nikolaus M. Wilpert NM, et al. Among authors: kaindl am. J Neurol. 2023 Oct;270(10):4593-4607. doi: 10.1007/s00415-023-11853-5. Epub 2023 Jul 29. J Neurol. 2023. PMID: 37515734 Free PMC article. Review.
Cerebral Abnormalities in Spina Bifida: A Neuropathological Study.
Paschereit F, Schindelmann KH, Hummel M, Schneider J, Stoltenburg-Didinger G, Kaindl AM. Paschereit F, et al. Among authors: kaindl am. Pediatr Dev Pathol. 2022 Mar-Apr;25(2):107-123. doi: 10.1177/10935266211040500. Epub 2021 Oct 6. Pediatr Dev Pathol. 2022. PMID: 34614376 Free PMC article.
176 results