Items where Author is "Stanescu, H C"

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Mencacci, N E and Rubio-Agusti, I and Zdebik, A and Asmus, F and Ludtmann, M H R and Ryten, M and Plagnol, V and Hauser, A K and Bandres-Ciga, S and Bettencourt, C and Forabosco, P and Hughes, D and Soutar, M M and Peall, K and Morris, H R and Trabzuni, D and Tekman, M and Stanescu, H C and Kleta, R and Carecchio, M and Zorzi, G and Nardocci, N and Garavaglia, B and Lohmann, E and Weissbach, A and Klein, C and Hardy, J and Pittman, A M and Foltynie, T and Abramov, A Y and Gasser, T and Bhatia, K P and Wood, N W (2015) A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia. American Journal of Human Genetics, 96 (6). pp. 938-47.

Zdebik, A A and Mahmood, F and Stanescu, H C and Kleta, R and Bockenhauer, D and Russell, C (2013) Epilepsy in kcnj10 Morphant Zebrafish Assessed with a Novel Method for Long-Term EEG Recordings. PLoS One, 8 (11).

Mahmood, F and Kaminskaite, M and Zdebik, A A and Stanescu, H C and Tobin, J and Beales, P L and Kleta, R and Bockenhauer, D and Russell, C (2013) Generation and validation of a zebrafish model of EAST (Epilepsy, Ataxia, Sensorineural deafness and Tubulopathy) syndrome. Disease Models and Mechanisms, 6 (3). p. 652.

This list was generated on Wed Oct 20 07:23:21 2021 BST.