Poland (PL)

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Journal article
Book chapter / Article in edited volumes
Authored book
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Edited Volume
Conference contribution
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Unpublished / Preprint

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Abstract

Journal

The SCCS Notes of Guidance for the testing of cosmetic ingredients and their safety evaluation, 11th revision, 30–31 March 2021, SCCS/1628/21 (2021) Bernauer U, Bodin L, Chaudhry Q, Coenraads PJ, Dusinska M, Ezendam J, Gaffet E, et al. Journal article Yade Documentation (3rd ed.) (2021) Smilauer V, Angelidakis V, Catalano E, Caulk R, Chareyre B, Chèvremont W, Dorofeenko S, et al. Authored book, Manual COVID-19 vaccination in autoimmune disease (COVAD) survey protocol (2021) Sen P, Gupta L, Lilleker JB, Aggarwal V, Kardes S, Milchert M, Gheita T, et al. Journal article The Puzzle of Punitive Memory Laws: New Insights into the Origins and Scope of Punitive Memory Laws (2021) Bachmann K, Lyubashenko I, Garuka C, Baranowska G, Pavlaković V Journal article Salivary Gland Carcinoma in Children and Adolescents: The Expert/Partner Diagnosis and Treatment Recommendations (2021) Bisogno G, Schneider D, Ferrari A, Stachowicz-Stencel T, Rascon J, Synakiewicz A, Agaimy A, et al. Conference contribution Efficacy and safety of high-dose lanreotide autogel in patients with progressive pancreatic or midgut neuroendocrine tumours: CLARINET FORTE phase 2 study results (2021) Pavel ME, Ćwikła JB, Lombard-Bohas C, Borbath I, Shah T, Pape UF, Capdevila J, et al. Journal article Regulated on Activation, Normal T cell Expressed and Secreted (RANTES) drives the resolution of allergic asthma (2021) Li N, Mirzakhani H, Kiefer A, Kölle J, Vuorinen T, Rauh M, Yang Z, et al. Journal article Algorithmic approach to cosmological coherent state expectation values in loop quantum gravity (2021) Liegener K, Rudnicki L Journal article Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis (2021) Escala-Garcia M, Canisius S, Keeman R, Beesley J, Anton-Culver H, Arndt V, Augustinsson A, et al. Journal article Exome sequencing implicates a novel heterozygous missense variant in DSTYK in autosomal dominant lower urinary tract dysfunction and mild hereditary spastic paraparesis. (2021) Vidic C, Zaniew M, Jurga S, Thiele H, Reutter HM, Hilger AC Journal article