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Oct 2026

AUTOSOMAL RECESSIVE AXONAL NEUROPATHY WITH NEUROMYOTONIA CAUSED BY A MUTATION IN THE HINT1 GENE: A REPORT OF TWO CLINICAL CASES

Hereditary sensorimotor neuropathies are characterized by high genetic heterogeneity, which complicates their diagnosis. Autosomal recessive axonal neuropathy with neuromyotonia (ARAN-NM), associated with mutations in the HINT1 gene, is a rare but clinically recognizable disease. Description of clinical cases is import...

I. Komarova, V. Zykov, A. S. Rubtsova et al. · 0 citations
Aug 2026

[Informative value of instrumental methods in assessing the anatomical and functional state of the corticospinal tract in children with severe traumatic brain injury].

OBJECTIVE To compare motor recovery in children with severe traumatic brain injury (TBI) with findings from functional and imaging diagnostic techniques based on the age-dependent theory of motor development. MATERIAL AND METHODS The study included 43 children (26 boys and 17 girls), aged 5 to 17 years, with severe T...

D. S. Kanshina, I. Mel'nikov, M. V. Ublinsky et al. · 0 citations

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