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Akademický článek
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Publikováno v:
Revista Jurídica Portucalense, Iss 26 (2019)
O presente trabalho almeja uma reflexão e análise oportunas em torno da temática dos acordos parassociais sobre o exercício de funções de administração, tal como a mesma é tratada, em especial, na sua relação com a proibição prevista no
Externí odkaz:
https://doaj.org/article/2dc0acc34f584284ac559e5df76025d0
Akademický článek
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Publikováno v:
Revista Jurídica Portucalense, Iss 23 (2018)
O presente trabalho almeja uma reflexão em torno da questão de saber em que medida devemos recear como discriminatório, por contrário à igualdade de género e remissivo para a secundarização e sombra social e histórica das Mulheres, aquilo a
Externí odkaz:
https://doaj.org/article/a2cc439fb59347958bbb0a156fa559fc
Publikováno v:
Revista Jurídica Portucalense, Iss 22 (2018)
O presente trabalho almeja uma reflexão em torno da temática do rapto internacional de crianças, tal como a mesma é abordada em especial na sua relação com os respectivos instrumentos de resolução. Este assunto apresenta, de resto, inquestio
Externí odkaz:
https://doaj.org/article/7bb6db6eab854fdeb53e3240b71d6d8d
Autor:
Vivekanandam, V, Männikkö, R, Skorupinska, I, Germain, L, Gray, B, Wedderburn, S, Kozyra, D, Sud, R, James, N, Holmes, S, Savvatis, K, Fialho, D, Merve, A, Pattni, J, Farrugia, M, Behr, ER, Marini-Bettolo, C, Hanna, MG, Matthews, E
Andersen Tawil Syndrome (ATS) is a neurological channelopathy caused by mutations in the KCNJ2 gene that encodes the ubiquitously expressed Kir2.1 potassium channel. The syndrome is characterised by episodic weakness, cardiac arrythmias and dysmorphi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::669d9a7a88132b38d6ed0a0e62dc137e
https://openaccess.sgul.ac.uk/id/eprint/113976/1/awab445.pdf
https://openaccess.sgul.ac.uk/id/eprint/113976/1/awab445.pdf
Akademický článek
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Autor:
Ribeiro, A, Suetterlin, KJ, Skorupinska, I, Tan, SV, Morrow, JM, Matthews, E, Hanna, MG, Fialho, D
INTRODUCTION/AIMS: The aim of this study was to evaluate the sensitivity of the long exercise test (LET) in the diagnosis of periodic paralysis (PP) and assess correlations with clinical phenotypes and genotypes. METHODS: From an unselected cohort of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::5ba46b38ed4d03ac23e7e6accdf2d6ec
https://openaccess.sgul.ac.uk/id/eprint/113910/1/mus.27465.pdf
https://openaccess.sgul.ac.uk/id/eprint/113910/1/mus.27465.pdf
Autor:
Suetterlin, K, Matthews, E, Sud, R, McCall, S, Fialho, D, Burge, J, Jayaseelan, D, Haworth, A, Sweeney, MG, Kullmann, DM, Schorge, S, Hanna, MG, Männikkö, R
High throughput DNA sequencing is increasingly employed to diagnose single gene neurological and neuromuscular disorders. Large volumes of data present new challenges in data interpretation and its useful translation into clinical and genetic counsel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::3aba0bee89cdf8b62a0959bff6cf2733
https://openaccess.sgul.ac.uk/id/eprint/113743/11/awab344.pdf
https://openaccess.sgul.ac.uk/id/eprint/113743/11/awab344.pdf
Our work aims to reflect on the reasons that guide the enshrining of the rules related to advertising directed to minors, with particular emphasis on the most recent restrictions on advertising directed to minors under 16 years related to foodstuffs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::138491d112fc1f74da56b7421a19ee55
https://doi.org/10.51389/ufbn1959
https://doi.org/10.51389/ufbn1959