Zobrazeno 1 - 5
of 5
pro vyhledávání: '"S. A. Klushnikov"'
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 6, Iss 3, Pp 47-52 (2017)
Cerebrovascular diseases are the major cause of morbidity and mortalityamong adults. The extensive development of various diagnosticmethods and their introduction into routine practice increasedthe detection of previously underappreciated and unknown
Externí odkaz:
https://doaj.org/article/65d7066f096c4ff1b52b4018f6678fea
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 8, Iss 4, Pp 9-14 (2017)
The article presents the results of ultrasound studies inpatients with hereditary motor and sensory neuropathy, orCharcot-Marie-Tooth disease (CMT). Based on standardelectroneuromiography, the patients were divided into two groupswith demyelinating (
Externí odkaz:
https://doaj.org/article/5fc76886d4f142aea4ef67987b1bfd26
Autor:
N. G. Savitskaya, S. S. Nikitin, S. N. Illarioshkin, S. A. Klushnikov, I. A. Ivanova-Smolenskaya, A. V. Ostaphyichuk
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 5, Iss 4, Pp 29-32 (2017)
We present results of clinical and electrophysological analysis of34 patients with recurrent facial neuropathy (rFN). Its frequency(10.9%) among all forms of facial neuropathies was determined,and clinical and EMG characteristics, as well as possible
Externí odkaz:
https://doaj.org/article/6c0c583769934d22ab52b042840ca63e
Autor:
M. V. Ershova, S. N. Illarioshkin, V. S. Sukhorukov, S. A. Klushnikov, T. N. Phedorova, I. A. Ivanova-Smolenskaya
Publikováno v:
Neurology Bulletin. :5-11
Some lesions were revealed in the system of oxidation mitochondrial phosphorylation in Fredreich disease, as well as their correlation with the disease course at its different clinical variants. A vivid tendency has been traced to normalization of th
Autor:
I. A. Ivanova-Smolenskaja, V. P. Phedotov, S. S. Nikitin, S. N. Illarioshkin, N. G. Savitskaja, S. A. Klushnikov
Publikováno v:
Neurology Bulletin. :5-9
Clinico-electrophysiological analysis of the most common in Russia family selection, having a particular form of demyelinization neuropathy hereditary neuropathy with predisposition to compression paralyses (HNPCP) has been presented. In all the fami