Diffusion Tensor Imaging And Tractography In Autistic, Dysphasic, And Healthy Control Children

Autor: Hrdlicka M, Sanda J, Urbanek T, Kudr M, Dudova I, Kickova S, Pospisilova L, Mohaplova M, Maulisova A, Krsek P, Kyncl M, Blatny M, Komarek V

Publikováno v: Neuropsychiatric Disease and Treatment, Vol Volume 15, Pp 2843-2852 (2019)

Michal Hrdlicka,1 Jan Sanda,2 Tomas Urbanek,3 Martin Kudr,4 Iva Dudova,1 Stepanka Kickova,1 Lenka Pospisilova,1,5 Marketa Mohaplova,1 Alice Maulisova,4 Pavel Krsek,4 Martin Kyncl,2 Marek Blatny,1,6 Vladimir Komarek4 1Department of Child Psychiatry, C

Externí odkaz: https://doaj.org/article/f1579f8421a14a62a1c25852640e1ceb

Distinctive MRI features of the epileptogenic zone in children with tuberous sclerosis

Autor: Jahodova, A., Krsek, P., Kyncl, M., Jezdik, P., Kudr, M., Komarek, V., Jayakar, P., Miller, I., Resnick, T., Duchowny, M.

Publikováno v: In European Journal of Radiology April 2014 83(4):703-709

Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders

Autor: Lal, D., May, P., Perez-Palma, E., Samocha, K. E., Kosmicki, J. A., Robinson, E. B., Moller, R. S., Krause, R., Nurnberg, P., Weckhuysen, S., De Jonghe, P., Guerrini, R., Niestroj, L. M., Du, J., Marini, C., Balling, R., Barisic, N., Baulac, S., Caglayan, H., Craiu, D. C., Depienne, C., Helbig, I., Hjalgrim, H., Hoffman-Zacharska, D., Jahn, J., Klein, K. M., Koeleman, B. P. C., Komarek, V., Leguern, E., Lehesjoki, A. -E., Lemke, J. R., Lerche, H., Linnankivi, T., Muhle, H., Pal, D. K., Palotie, A., Rosenow, F., Schubert-Bast, S., Selmer, K., Serratosa, J. M., Stephani, U., Sterbova, K., Striano, P., Suls, A., Talvik, T., Von Spiczak, S., Weber, Y. G., Zara, F., Ware, J. S., Kurki, M., Gormley, P., Tang, S., Wu, S., Biskup, S., Poduri, A., Neubauer, B. A., Helbig, K. L., Majithia, A. R., Daly, M. J.

Publikováno v: Genome medicine
Genome Medicine, Vol 12, Iss 1, Pp 1-12 (2020)
Genome Medicine
Lal, D, May, P, Perez-Palma, E, Samocha, K E, Kosmicki, J A, Robinson, E B, Møller, R S, Krause, R, Nürnberg, P, Weckhuysen, S, De Jonghe, P, Guerrini, R, Niestroj, L M, Du, J, Marini, C, Ware, J S, Kurki, M, Gormley, P, Tang, S, Wu, S, Biskup, S, Poduri, A, Neubauer, B A, Koeleman, B P C, Helbig, K L, Weber, Y G, Helbig, I, Majithia, A R, Palotie, A, Daly, M J & EuroEPINOMICS RES Consortium 2020, ' Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders ', Genome Medicine, vol. 12, 28 . https://doi.org/10.1186/s13073-020-00725-6

Background Classifying pathogenicity of missense variants represents a major challenge in clinical practice during the diagnoses of rare and genetic heterogeneous neurodevelopmental disorders (NDDs). While orthologous gene conservation is commonly em

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b036557331bdae2c9f0cad2faa39ec2d
https://hdl.handle.net/10067/1686320151162165141

Chapter 37 Evolution of EEG and seizures in childhood

Autor: Komárek, V., Štěrbová, K., Faladová, L.

Publikováno v: In Supplements to Clinical Neurophysiology 2000 53:250-258

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