| HINT1 gene pathogenic variants: the most common cause of recessive hereditary motor and sensory neuropathies in Russian patients OA Shchagina, TB Milovidova, AF Murtazina, GE Rudenskaya, SS Nikitin, ... Molecular Biology Reports 47 (2), 1331-1337, 2020 | 19 | 2020 |
| Thoracic outlet syndrome: clinical and diagnostic features AF Murtazina, SS Nikitin, ES Naumova Neuromuscular Diseases 7 (4), 10-19, 2018 | 13* | 2018 |
| Bickerstaff brainstem encephalitis, acute transverse myelitis, and acute motor axonal neuropathy: diagnostic and treatment challenges in patients with concomitant syndromes … AF Murtazina, ES Naumova, SS Nikitin, LM Boriskina, AV Lagutin Neuromuscular Diseases 7 (3), 56-62, 2017 | 11* | 2017 |
| Clinical and genetic characteristics of autosomal recessive axonal neuropathy with neuromyotonia in Russian patients EL Dadali, SS Nikitin, SA Kurbatov, AF Murtazina, IV Sharkova, ... Neuromuscular Diseases 7 (3), 47-55, 2017 | 8* | 2017 |
| The first Russian patient with Native American myopathy A Murtazina, N Demina, P Chausova, O Shchagina, A Borovikov, E Dadali Genes 13 (2), 341, 2022 | 5 | 2022 |
| Conduction block as an electrophysiological phenomenon: a review of the literature SS Nikitin, AF Murtazina, DS Druzhinin Neuromuscular Diseases 9 (1), 12-23, 2019 | 5* | 2019 |
| Electrophysiological techniques for motor unit number estimation AF Murtazina, AI Belyakova-Bodina, AG Brutyan Human Physiology 44, 827-837, 2018 | 5* | 2018 |
| Genetic and clinical spectrum of GNE myopathy in Russia A Murtazina, S Nikitin, G Rudenskaya, I Sharkova, A Borovikov, P Sparber, ... Genes 13 (11), 1991, 2022 | 4 | 2022 |
| A case of hereditary motor and sensory neuropathy type IVA with unusual genealogy SA Kurbatov, TB Milovidova, VP Fedotov, AF Murtazina, GE Rudenskaya, ... Neuromuscular Diseases 8 (2), 75-83, 2018 | 4* | 2018 |
| Clinical and genetic characteristics of Nonaka myopathy (GNE-myopathy) in russian patients EL Dadali, IV Sharkova, GE Rudenskaya, SS Nikitin, AF Murtazina, ... Neuromuscular Diseases 9 (3), 56-66, 2019 | 3* | 2019 |
| Современные клиникогенетические представления об аутосомнорецессивных наследственных периферических нейропатиях АФ Муртазина, ОА Щагина, СС Никитин, ЕЛ Дадали, АВ Поляков Анналы клинической и экспериментальной неврологии 13 (1), 55-69, 2019 | 3 | 2019 |
| Причины ложной диагностики полимиозита у пациентов с дисферлинопатией: клинический случай СН Бардаков, АМ Емелин, СС Никитин, АН Хелковская-Сергеева, ... Нервно-мышечные болезни 12 (4), 73-87, 2022 | 2 | 2022 |
| POLR3A-ассоциированная гипомиелинизированная лейкодистрофия: описание клинического случая и обзор литературы АФ Муртазина, ТВ Маркова, АА Орлова, ОП Рыжкова, ОА Щагина, ... Нервно-мышечные болезни 11 (4), 48-54, 2021 | 2* | 2021 |
| Клинико-генетические характеристики дистальных артрогрипозов, обусловленных мутациями в гене PIEZO2 ТВ Маркова, ЕЛ Дадали, СС Никитин, АФ Муртазина, ОЛ Миронович, ... Нервно-мышечные болезни 11 (2), 48-55, 2021 | 2* | 2021 |
| Surgery for intractable epilepsy in a patient with encephalocele of the temporal lobe: a case report MS Semenov, AI Belyakova-Bodina, AF Murtazina, AG Brutyan, ... Zhurnal Voprosy Neirokhirurgii Imeni NN Burdenko 81 (6), 99-102, 2017 | 2 | 2017 |
| Комплексные геномные перестройки в этиологии «хромосомного фенотипа» МЕ Миньженкова, ЖГ Маркова, ДА Юрченко, АА Тарлычева, ... Медицинская генетика 21 (11), 44-47, 2022 | 1 | 2022 |
| Clinical and genetic characteristics of Charcot–Marie–Tooth disease type 4D (type Lom) in Russia AF Murtazina, OA Shchagina, TB Milovidova, EL Dadali, GE Rudenskaya, ... Neuromuscular Diseases 10 (2), 39-45, 2020 | 1 | 2020 |
| The Missing Piece of the Puzzle: Unveiling the Role of PTPN11 Gene in Multiple Osteochondromas in a Large Cohort Study A Borovikov, N Galeeva, A Marakhonov, A Murtazina, V Kadnikova, ... Human Mutation 2024, 2024 | | 2024 |
| Mild phenotype of CHAT-associated congenital myasthenic syndrome: case series A Murtazina, A Borovikov, A Marakhonov, A Sharkov, I Sharkova, ... Frontiers in Pediatrics 12, 2024 | | 2024 |
| Expanding the Phenotype of Hereditary Congenital Facial Paresis Type 3 A Murtazina, A Borovikov, A Kuchina, O Ovsova, M Bulakh, A Chukhrova, ... International Journal of Molecular Sciences 25 (1), 129, 2023 | | 2023 |
