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| Issue | Title | |
| Vol 7, No 1 (2015) | ALPERS-HUTTENLOCHER SYNDROME | Abstract similar documents |
| T. T. Batysheva, V. M. Trepilets, L. Ya. Akhadova, G. S. Golosnaya | ||
| "... Alpers-Huttenlocher syndrome is a rare mitochondrial disease connected with mutations ..." | ||
| Vol 4, No 2 (2012) | EPILEPSY IN CHILDREN WITH MYTOCHONDRIAL DISEASES: DIAGNOSTICS AND TREATMENT FEATURES | Abstract similar documents |
| N. N. Zavadenko, A. A. Kholin | ||
| "... Mitochondrial diseases (MD) represent a large clinically heterogeneous group of disorders ..." | ||
| Vol 12, No 4 (2020) | Features of brain electrical activity in adult patients with POLG-related disorders | Abstract similar documents |
| P. A. Fedin, E. P. Nuzhnyi, T. Yu. Noskova, Yu. A. Seliverstov, S. A. Klyushnikov, T. D. Krylova, P. G. Tsygankova, E. Yu. Zakharova, S. N. Illarioshkin | ||
| "... Introduction. Epilepsy is a common feature of mitochondrial disorders, including those associated ..." | ||
| Vol 15, No 4 (2023) | Epilepsy and MELAS syndrome: literature review and clinical observation | Abstract similar documents |
| А. М. Teplysheva, М. А. Glazova, R. N. Konovalov | ||
| "... MELAS syndrome (mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes) belongs ..." | ||
| Vol 9, No 4 (2017) | THE OPTIMIZED METHODS FOR DIAGNOSIS OF HEREDITARY FORMS OF EPILEPSY | Abstract similar documents |
| A. G. Malov | ||
| "... ; and in the case of a disease suspected for a mitochondrial mutation – the mitochondrial DNA sequencing. ..." | ||
| Vol 6, No 4 (2014) | МР-СПЕКТРОСКОПИЯ ПРИ МИТОХОНДРИАЛЬНЫХ ЭНЦЕФАЛОМИОПАТИЯХ | Abstract similar documents |
| , , , , , , , , | ||
| Vol 8, No 2 (2016) | PROTECTION OF BRAIN MITOCHONDRIA AGAINST MICRO STROKE-INDUCED INJURY: A STUDY OF ETHYLMETHYLHYDROXYPYRIDINE SUCCINATE IN EXPERIMENTAL MODEL USING TWO PHOTON LASER FLUORESCENT MICROSCOPY | Abstract similar documents |
| R. A. Afzalov, Yu. O. Kolikova, E. G. Pryazhnikov, D. V. Toptunov, L. S. Khirug | ||
| "... Objective. Mitochondrial injury plays a central role in neuronal death following ischemic stroke ..." | ||
| Vol 13, No 1 (2021) | Clinical case of epilepsy, hearing loss and mental retardation syndrome associated with mutations in SPATA5 gene | Abstract similar documents |
| T. V. Kozhanova, S. S. Zhilina, T. I. Meshcheryakova, E. G. Luk’yanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko, N. N. Zavadenko | ||
| "... leading to pathology with clinical manifestations mimicking mitochondrial disease. ..." | ||
| Vol 14, No 1 (2022) | Myoclonic epilepsy with ragged red fibers in childhood | Abstract similar documents |
| Z. G. Tadtaeva, A. N. Galustyan, М. Yu. Krivdina, V. V. Rusanovsky, E. A. Efet, A. Е. Krivoshein, N. A. Kuritsyna, О. A. Gromova | ||
| "... is associated with the most common (90% of cases) point mutation at position 8344 in the mitochondrial lysine ..." | ||
| Vol 16, No 1 (2024) | Postinfectious epilepsy: clinical and diagnostical features | Abstract PDF (Eng) similar documents |
| А. V. Vasilenko, А. Yu. Ulitin, L. S. Onishchenko, N. I. Ananyeva, R. V. Grebenshchikova, О. N. Gaykova, А. V. Ivanenko, S. S. Kolosov, S. А. Turanov, S. N. Chudievich | ||
| "... with earlier described mitochondrial encephalomyopathies (mitochondrial megaconia and pleioconia) as well ..." | ||
| 1 - 10 of 10 Items | ||
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