Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Ritz, Katja"'
Autor:
Denswil, Nerissa P., van der Wal, Allard C., Ritz, Katja, de Boer, Onno J., Aronica, Eleonora, Troost, Dirk, Daemen, Mat J.A.P.
Publikováno v:
In Atherosclerosis August 2016 251:78-84
Autor:
Ritz, Katja1,2, van Schaik, Barbera D. C.3, Jakobs, Marja E.1, van Kampen, Antoine H.3,4, Aronica, Eleonora5, Tijssen, Marina A.2, Baas, Frank1 f.baas@amc.uva.nl
Publikováno v:
European Journal of Human Genetics. Apr2011, Vol. 19 Issue 4, p438-444. 7p. 1 Color Photograph, 1 Diagram, 3 Charts, 1 Graph.
Autor:
Ritz, Katja, Schär, Giuliana
Einleitung: Chronische Lungenerkrankungen führen durch das Verändern des Atemmusters und durch Atemhilfsstellungen zu Nackenschmerzen. Ob eine umgekehrte Verbindung ebenfalls besteht, war bisher nicht bekannt. Ziel: Diese Arbeit soll mögliche Zusa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf25cc3c7f8dd7a186efc204d319ce93
Publikováno v:
In Parkinsonism and Related Disorders July 2014 20(7):782-785
Autor:
Schaefer, Antje, te Riet, Joost, Ritz, Katja, Hoogenboezem, Mark, Anthony, Eloise C., Mul, Frederik P.J., de Vries, Carlie J., Daemen, M. J., Figdor, Carl G., van Buul, Jaap D., Hordijk, Peter L.
Publikováno v:
Journal of Cell Science, 127(22). Company of Biologists Ltd
Schaefer, A, te Riet, J, Ritz, K, Hoogenboezem, M, Anthony, E C, Mul, F P J, de Vries, C J, Daemen, M J, Figdor, C G, van Buul, J D & Hordijk, P L 2014, ' Correction to Actin-binding proteins differentially regulate endothelial cell stiffness, ICAM-1 function and neutrophil transmigration [Journal of Cell Science 127, (2014) 4470-4482] ', Journal of Cell Science, vol. 127, no. 22, pp. 4985 . https://doi.org/10.1242/jcs.164814
Schaefer, A, te Riet, J, Ritz, K, Hoogenboezem, M, Anthony, E C, Mul, F P J, de Vries, C J, Daemen, M J, Figdor, C G, van Buul, J D & Hordijk, P L 2014, ' Correction to Actin-binding proteins differentially regulate endothelial cell stiffness, ICAM-1 function and neutrophil transmigration [Journal of Cell Science 127, (2014) 4470-4482] ', Journal of Cell Science, vol. 127, no. 22, pp. 4985 . https://doi.org/10.1242/jcs.164814
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::974fbf251ac79a850ebf36294750bc2b
https://research.vumc.nl/en/publications/d5b80b01-2fcf-4af8-990e-34fdff4dca88
https://research.vumc.nl/en/publications/d5b80b01-2fcf-4af8-990e-34fdff4dca88
Autor:
Groen, Justus L., Simón-Sánchez, Javier, Ritz, Katja, Bochdanovits, Zoltán, Fang, Yue, van Hilten, Jacobus J., Aramideh, Majid, van de Warrenburg, Bart P., Boon, Agnita J.W., Baas, Frank, Heutink, Peter, Tijssen, Marina A.J.
Publikováno v:
In Parkinsonism and Related Disorders March 2013 19(3):346-349
Autor:
Groen, Justus L., Ritz, Katja, Tanck, Michael W., van de Warrenburg, Bart P., van Hilten, Jacobus J., Aramideh, Majid, Baas, Frank, Tijssen, Marina A. J.
Publikováno v:
Movement disorders, 28(6), 827-831. John Wiley and Sons Inc.
Movement Disorders, 28(6), 827-831. Wiley
Movement Disorders, 28(6), 827-831. Wiley
BACKGROUND: Studies of genetic association between TOR1A and adult-onset primary torsion dystonia have contradictory results. METHODS: The authors genotyped TOR1A single nucleotide polymorphisms rs1801968, rs2296793, rs1182 and rs3842225 in a cohort
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::da82dcdc31e50fc0f512887e3e0b9dda
https://pure.amc.nl/en/publications/is-tor1a-a-risk-factor-in-adultonset-primary-torsion-dystonia(4cd5c1e0-ef42-4848-aa47-1a9971608d4c).html
https://pure.amc.nl/en/publications/is-tor1a-a-risk-factor-in-adultonset-primary-torsion-dystonia(4cd5c1e0-ef42-4848-aa47-1a9971608d4c).html
Autor:
Ritz, Katja, Groen, Justus L., Kruisdijk, Jose J. M., Baas, Frank, Koelman, Johannes H. T. M., Tijssen, Marina A. J.
Publikováno v:
Movement Disorders, 24(9), 1390-1392. Wiley
Movement disorders, 24(9), 1390-1392. John Wiley and Sons Inc.
Movement disorders, 24(9), 1390-1392. John Wiley and Sons Inc.
Task-specific focal upper limb dystonia can be part of the phenotypic spectrum of different types of hereditary dystonia. We investigated whether writer's cramp as presenting symptom is associated with mutations in DYT11, DYT16, or with the DYT1 GAG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::220d33df22d32a312037422264458f7c
https://research.rug.nl/en/publications/3a8bace7-9589-478d-ae46-86dac1adde69
https://research.rug.nl/en/publications/3a8bace7-9589-478d-ae46-86dac1adde69
Autor:
Contarino, Maria Fiorella, Berger-Plantinga, Elles, Foncke, Elisabeth M. J., Ritz, Katja, Mellema, Jonke, Baas, Frank, Speelman, Johannes D., de Koning-Tijssen, Marina
Publikováno v:
Movement disorders, 23(14), 1998-2003. John Wiley and Sons Inc.
Movement Disorders, 23(14), 1998-2003. Wiley
Movement Disorders, 23(14), 1998-2003. Wiley
We describe a large family with a primary focal dystonia from a small Dutch village on a former island. Twenty-four individuals spanning three generations were examined by two movement-disorder neurologists. Two other movement-disorder neurologists e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c95e22fcf9a7c91e8fe68a4caa3d830e
https://pure.amc.nl/en/publications/clinical-and-genetic-characterization-of-a-large-dutch-family-with-primary-focal-dystonia(5c070089-bcfc-4de8-a68c-ddca3a65569b).html
https://pure.amc.nl/en/publications/clinical-and-genetic-characterization-of-a-large-dutch-family-with-primary-focal-dystonia(5c070089-bcfc-4de8-a68c-ddca3a65569b).html