Search Results - "Tsargush, V. A."
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A new mutation in the TYMP-gene: clinical and morphological characteristics of a patient with MNGIE syndrome
Published in Nervno-myshechnye bolezni (13-12-2022)“…Mitochondrial neurogastrointestinal encephalomyopathy is an extremely rare (1–9:1 000 000, Orphanet, 2021) multisystem genetic disease caused by mutations in…”
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Reasons for misdiagnosis of polymyositis in patients with dysferlinopathy: a clinical case
Published in Nervno-myshechnye bolezni (13-12-2022)“…Differential diagnosis of inflammatory myopathies with hereditary muscular dystrophies accompanied by a secondary inflammatory process is a time‑consuming…”
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Therapeutic apheresis in the complex pathogenetic therapy of anti-NMDA encephalitis associated with ovarian teratoma at a late stage of the disease
Published in Nervno-myshechnye bolezni (29-12-2021)“…Anti‑NMDA encephalitis is a rare autoimmune disease of the central nervous system caused by the synthesis of autoantibodies to the NR1/NR2 subunits of the NMDA…”
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The clinical case of limb-girdle muscle dystrophy 2Q associated with myasthenic syndrome and lung damage
Published in Nervno-myshechnye bolezni (20-11-2019)“…Limb-girdle muscle dystrophy 2Q is one of the rarest forms of plectinopathies and is represented by an isolated muscular dystrophic syndrome, according to two…”
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Therapeutic apheresis in the complex pathogenetic therapy of anti-NMDA encephalitis associated with ovarian teratoma at a late stage of the disease
Published in Nervno-myshechnye bolezni (01-01-2021)“…Abstract Anti‑NMDA encephalitis is a rare autoimmune disease of the central nervous system caused by the synthesis of autoantibodies to the NR1/NR2 subunits of…”
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