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| Issue | Title | |
| Vol 10, No 4 (2018) | Presurgical non-invasive diagnosis of focal cortical dysplasia | Abstract similar documents |
| S. V. Mirkhaydarov | ||
| "... . Focal cortical dysplasia is the most common abnormality of cortical development that is often associated ..." | ||
| Vol 11, No 4 (2019) | The use of intraoperative ultrasound in patients with focal cortical dysplasia: preliminary observations | Abstract similar documents |
| A. A. Sufianov, S. V. Mirhaydarov, Yu. A. Yakimov, O. M. Klimenko, A. A. Skripnikov, S. Z. Stefanov, O. N. Sadykova, R. S. Talybov, R. A. Sufianov | ||
| "... is the main objective of the surgeon. When a neurosurgeon operates focal cortical dysplasia (FCD), he/she ..." | ||
| Vol 4, No 2 (2012) | FOCAL CORTICAL DYSPLASIA: ALGORITHM OF PREOPERATIVE EXAMINATION | Abstract similar documents |
| S. O. Ayvazyan | ||
| "... evaluation and surgical treatment of focal cortical dysplasia in children. Particular attention is paid ..." | ||
| Vol 14, No 3 (2022) | Temporal lobe white matter pathways: clinical and anatomical examination related to surgery of drug-resistant structural focal epilepsy | Abstract similar documents |
| A. A. Sufianov, I. S. Shelyagin, K. Simfukwe, E. S. Markin, S. Zh. Stefanov, Yu. A. Yakimov, P. O. Akimova, R. A. Sufianov | ||
| "... Background. Detected temporal lobe focal cortical dysplasia (FCD) often results in developing drug ..." | ||
| Vol 15, No 4 (2023) | DEPDC5-related familial focal epilepsy | Abstract similar documents |
| T. V. Kozhanova, S. S. Zhilina, L. M. Sushko, E. G. Lukyanova, K. V. Osipova, A. I. Krapivkin, N. N. Zavadenko | ||
| "... in DEPDC5 gene were found in two probands and paired fathers with epilepsy. Focal cortical dysplasia ..." | ||
| Vol 16, No 4 (2024) | DEPDC5 mutations in familial epilepsy syndrome: genetic insights and therapeutic approaches | Abstract PDF (Eng) similar documents |
| M. K.C. Diallo, S. Mukesh, L. Kapil, R. Singla, D. Tar, S. N. Tammineedi, E. Singer, H. Chhayani, K. Arumaithurai, U. K. Patel, R. Arora | ||
| "... спорадическую мутацию в гене DEPDC5 с полиморфизмом p.R389H неизвестного значения. Клинический случай. Девочка ..." | ||
| Vol 11, No 3 (2019) | Recommendations of the Russian League Against Epilepsy (RLAE) on the use of magnetic resonance imaging in the diagnosis of epilepsy | Abstract similar documents |
| G. N. Avakyan, D. V. Blinov, A. A. Alikhanov, E. M. Perepelova, V. A. Perepelov, S. G. Burd, A. V. Lebedeva, G. G. Avakyan | ||
| "... детской популяции. Результаты. Всем пациентам с судорожными приступами вскоре после первого приступа, или ..." | ||
| 1 - 7 of 7 Items | ||
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