Zielonka E - Search Results

1

Corneal Abnormalities Are Novel Clinical Feature in Wolfram Syndrome.

Waszczykowska A, Zmysłowska A, Braun M, Zielonka E, Ivask M, Koks S, Jurowski P, Młynarski W. Waszczykowska A, et al. Among authors: zielonka e. Am J Ophthalmol. 2020 Sep;217:140-151. doi: 10.1016/j.ajo.2020.04.012. Epub 2020 Apr 23. Am J Ophthalmol. 2020. PMID: 32335055

2

Electron microscopic and confocal laser microscopy analysis of amyloid plaques in chronic wasting disease transmitted to transgenic mice.

Sikorska B, Gajos A, Bogucki A, Zielonka E, Sigurdson C, Liberski PP. Sikorska B, et al. Among authors: zielonka e. Prion. 2017 Nov 2;11(6):431-439. doi: 10.1080/19336896.2017.1384109. Prion. 2017. PMID: 29105545 Free PMC article.

3

Sclerodermiform Cell Epithelioma of the Palpebromalar Region.

Gerin M, Tooulou M, Zielonka E. Gerin M, et al. Among authors: zielonka e. Plast Reconstr Surg Glob Open. 2024 May 3;12(5):e5796. doi: 10.1097/GOX.0000000000005796. eCollection 2024 May. Plast Reconstr Surg Glob Open. 2024. PMID: 38706470 Free PMC article.

4

Enhanced pro-apoptosis gene signature following the activation of TAp63α in oocytes upon γ irradiation.

Fester N, Zielonka E, Goldmann J, Frombach AS, Müller-Kuller U, Gutfreund N, Riegel K, Smits JGA, Schleiff E, Rajalingam K, Zhou H, Simm S, Dötsch V. Fester N, et al. Among authors: zielonka e. Cell Death Dis. 2022 Mar 4;13(3):204. doi: 10.1038/s41419-022-04659-2. Cell Death Dis. 2022. PMID: 35246516 Free PMC article.

5

The Small Non-coding Vault RNA1-1 Acts as a Riboregulator of Autophagy.

Horos R, Büscher M, Kleinendorst R, Alleaume AM, Tarafder AK, Schwarzl T, Dziuba D, Tischer C, Zielonka EM, Adak A, Castello A, Huber W, Sachse C, Hentze MW. Horos R, et al. Among authors: zielonka em. Cell. 2019 Feb 21;176(5):1054-1067.e12. doi: 10.1016/j.cell.2019.01.030. Epub 2019 Feb 14. Cell. 2019. PMID: 30773316 Free article.

6

Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study.

McNulty P, Pilcher R, Ramesh R, Necuiniate R, Hughes A, Farewell D, Holmans P, Jones L; REGISTRY Investigators of the European Huntington's Disease Network. McNulty P, et al. J Huntingtons Dis. 2018;7(3):209-222. doi: 10.3233/JHD-170263. J Huntingtons Dis. 2018. PMID: 30103338

7

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.

Moss DJH, Pardiñas AF, Langbehn D, Lo K, Leavitt BR, Roos R, Durr A, Mead S; TRACK-HD investigators; REGISTRY investigators; Holmans P, Jones L, Tabrizi SJ. Moss DJH, et al. Lancet Neurol. 2017 Sep;16(9):701-711. doi: 10.1016/S1474-4422(17)30161-8. Epub 2017 Jun 20. Lancet Neurol. 2017. PMID: 28642124

8

Clinical manifestations of intermediate allele carriers in Huntington disease.

Cubo E, Ramos-Arroyo MA, Martinez-Horta S, Martínez-Descalls A, Calvo S, Gil-Polo C; European HD Network. Cubo E, et al. Neurology. 2016 Aug 9;87(6):571-8. doi: 10.1212/WNL.0000000000002944. Epub 2016 Jul 8. Neurology. 2016. PMID: 27402890

9

[Abdominal necrotizing fasciitis after caesarean delivery].

Barant S, Radbata D, Oberweis D, Jacobs D, Marecaux G, Zielonka E, Maréchal M. Barant S, et al. Among authors: zielonka e. Rev Med Brux. 2016;37(3):178-182. Rev Med Brux. 2016. PMID: 28525192 French.

10

The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients.

Metzger S, Walter C, Riess O, Roos RA, Nielsen JE, Craufurd D; REGISTRY Investigators of the European Huntington’s Disease Network; Nguyen HP. Metzger S, et al. PLoS One. 2013 Jul 22;8(7):e68951. doi: 10.1371/journal.pone.0068951. Print 2013. PLoS One. 2013. PMID: 23894380 Free PMC article.

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