Royal Devon & Exeter NHS Foundation Trust


Klinik

Standort der Organisation:
Exeter, Großbritannien (UK)


Publikationen in Kooperation mit FAU-Wissenschaftern


Blok, L.S., Rousseau, J., Twist, J., Ehresmann, S., Takaku, M., Venselaar, H.,... Campeau, P.M. (2018). CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nature Communications, 9(1). https://dx.doi.org/10.1038/s41467-018-06014-6
Azizi, M., Schmieder, R., Mahfoud, F., Weber, M.A., Daemen, J., Davies, J.,... Mauri, L. (2018). Endovascular ultrasound renal denervation to treat hypertension (RADIANCE-HTN SOLO): a multicentre, international, single-blind, randomised, sham-controlled trial. Lancet. https://dx.doi.org/10.1016/S0140-6736(18)31082-1
Townsend, R.R., Mahfoud, F., Kandzari, D.E., Kario, K., Pocock, S., Weber, M.A.,... Böhm, M. (2017). Catheter-based renal denervation in patients with uncontrolled hypertension in the absence of antihypertensive medications (SPYRAL HTN-OFF MED): a randomised, sham-controlled, proof-of-concept trial. Lancet. https://dx.doi.org/10.1016/S0140-6736(17)32281-X
Schmieder, R., Ott, C., Toennes, S.W., Bramlage, P., Gertner, M., Dawood, O.,... Lobo, M.D. (2017). Phase II randomized sham-controlled study of renal denervation for individuals with uncontrolled hypertension - WAVE IV. Journal of Hypertension. https://dx.doi.org/10.1097/HJH.0000000000001584
Meyer, E., Carss, K.J., Rankin, J., Nichols, J.M.E., Grozeva, D., Joseph, A.P.,... Kurian, M.A. (2016). Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia. Nature Genetics. https://dx.doi.org/10.1038/ng.3740

Zuletzt aktualisiert 2017-06-05 um 07:01