N. Zhurkova

AUTOSOMAL RECESSIVE PERIPHERAL NEUROPATHY WITH NEUROMYOTONIA (ARAN-NM): DESCRIPTION OF A CLINICAL CASE CONFIRMED BY A MUTATION IN THE HINT1 GENE

A. Kurenkov, O. Klochkova, K. Savostyanov, 2017 .

Diagnosis and treatment of the long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHAD) in a 8 months old infant

O. Usoltseva, L. Gandaeva, E. Kulebina, 2020 .