Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Suetterlin K"'
Autor:
Sütterlin, K. R., Wysocki, A., Ivlev, A. V., Räth, C., Thomas, H. M., Rubin-Zuzic, M., Goedheer, W. J., Fortov, V. E., Lipaev, A. M., Molotkov, V. I., Petrov, O. F., Morfill, G. E., Löwen, H.
The dynamical onset of lane formation is studied in experiments with binary complex plasmas under microgravity conditions. Small microparticles are driven and penetrate into a cloud of big particles, revealing a strong tendency towards lane formation
Externí odkaz:
http://arxiv.org/abs/0812.3091
Akademický článek
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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
Autor:
Suetterlin, K.1,2,3 (AUTHOR), Mannikko, R.2 (AUTHOR), Matthews, E.4 (AUTHOR), Maitland, S.5 (AUTHOR), Greensmith, L.2 (AUTHOR), Hanna, M.2 (AUTHOR), Tan, S.2,6 (AUTHOR)
Publikováno v:
Neuromuscular Disorders. 2024 Supplement 1, Vol. 43, pN.PAG-N.PAG. 1p.
Akademický článek
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Autor:
Suetterlin, K, Männikkö, R, Flossmann, E, Sud, R, Fialho, D, Vivekanandam, V, James, N, Gossios, TD, Hanna, MG, Savvatis, K, Matthews, E
Andersen-Tawil syndrome (ATS) is a rare autosomal dominant neuromuscular disorder due to mutations in the KCNJ2 gene. The classical phenotype of ATS consists of a triad of periodic paralysis, cardiac conduction abnormalities and dysmorphic features.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::552ee95e51f40d797fec831bcb0490df
Autor:
Matthews, E, Neuwirth, C, Jaffer, F, Scalco, RS, Fialho, D, Parton, M, Rayan, D, Suetterlin, K, Sud, R, Spiegel, R, Mein, R, Houlden, H, Schaefer, A, Healy, E, Palace, J, Quinlivan, R, Treves, S, Holton, JL, Jungbluth, H, Hanna, MG
Publikováno v:
Matthews, E, Neuwirth, C, Jaffer, F, Scalco, R S, Fialho, D, Parton, M, Raja Rayan, D, Suetterlin, K, Sud, R, Spiegel, R, Mein, R, Houlden, H, Schaefer, A, Healy, E, Palace, J, Quinlivan, R, Treves, S, Holton, J L, Jungbluth, H & Hanna, M G 2018, ' Atypical periodic paralysis and myalgia : A novel RYR1 phenotype ', Neurology, vol. 90, no. 5, pp. e1-e7 . https://doi.org/10.1212/WNL.0000000000004894
OBJECTIVE: To characterize the phenotype of patients with symptoms of periodic paralysis (PP) and ryanodine receptor (RYR1) gene mutations.METHODS: Cases with a possible diagnosis of PP but additional clinicopathologic findings previously associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::52310ab2fbe85b5f04084c81b7647c3f
http://ora.ox.ac.uk/objects/uuid:
http://ora.ox.ac.uk/objects/uuid:
Autor:
Suetterlin, K., Sud, R., Burge, J., McCall, S., Fialho, D., Haworth, A., Sweeney, M., Houlden, H., Schorge, S., Matthews, E., Hanna, M., Mannikko, R.
Publikováno v:
In Neuromuscular Disorders October 2017 27 Supplement 2:S165-S165
Autor:
Molenaar, J., Verhoeven, J., Voermans, N., Mathieu, J., Vattemi, G., Franques, J., Kuntzer, T., Guyant-Marechal, L., Vicart, S., Behin, A., Erasmus, C., Brandom, B., Matthews, E., Suetterlin, K., van Engelen, B., Sternberg, D., Eymard, B.
Publikováno v:
In Neuromuscular Disorders October 2017 27 Supplement 2:S164-S164
Autor:
Suetterlin, K., Sud, R., Burge, J., McCall, S., Fialho, D., Haworth, A., Sweeney, M.G., Houlden, H., Schorge, S., Matthews, E., Hanna, M.G., Männikkö, R.
Publikováno v:
In Neuromuscular Disorders March 2017 27 Supplement 1:S34-S34