Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Bart F L, van Nuenen"'
Autor:
Stijn B. J. Teijink, Niels Pesser, Jens Goeteyn, Renée J. Barnhoorn, Marc R. H. M. van Sambeek, Bart F. L. van Nuenen, Hugh A. Gelabert, Joep A. W. Teijink
Publikováno v:
Diagnostics, Vol 13, Iss 9, p 1625 (2023)
Thoracic outlet syndrome is an uncommon and controversial syndrome. Three different diagnoses can be made based on the compressed structure, arterial TOS, venous TOS, and neurogenic TOS, though combinations do exist as well. Diagnosing NTOS is diffic
Externí odkaz:
https://doaj.org/article/3c8401a67d3b46a0b552039a97a414a5
Autor:
Amée F. Wolters, Bart F. L. van Nuenen
Publikováno v:
Neurological Sciences, 41(4), 967-968. Springer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e64aead8d2f1bad22ce58a2364adf4f7
https://cris.maastrichtuniversity.nl/en/publications/7cbb9709-9fae-46d0-9953-98cbc73a2ac8
https://cris.maastrichtuniversity.nl/en/publications/7cbb9709-9fae-46d0-9953-98cbc73a2ac8
Autor:
Michael A, van Es, Jan H, Veldink, Helenius J, Schelhaas, Bastiaan R, Bloem, Peter, Sodaar, Bart F L, van Nuenen, Marcel, Verbeek, Bart P, van de Warrenburg, Leonard H, van den Berg
Publikováno v:
Journal of neurology, neurosurgery, and psychiatry. 85(12)
Autor:
Bart F L, van Nuenen, Thilo, van Eimeren, Joyce P M, van der Vegt, Carsten, Buhmann, Christine, Klein, Bastiaan R, Bloem, Hartwig R, Siebner
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 24
Mutations in the Parkin (PARK2) and PINK1 gene (PARK 6) can cause recessively inherited Parkinson's disease (PD). The presence of a single Parkin or PINK1 mutation is associated with a dopaminergic nigrostriatal dysfunction and conveys an increased r