Search Results - K. V. Savostyanov

Clinical Cases of Leukoencephalopathy with Predominant Lesion of the Brain Stem, Spinal Cord and High Blood Lactate in the MR Spectroscopy (Mitochondrial Aspartyl-tRNASynthetase De... by Ye. P. Kolesnikova, L. M. Kuzenkova, K. V. Savostyanov, O. V. Globa, T. V. Podkletnova

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Molecular and Genetic Basis of Hereditary Connective-Tissue Diseases Accompanied by Frequent Fractures by G. T. Yakhyaeva, L. S. Namazova-Baranova, T. V. Margieva, N. V. Zhurkova, A. A. Pushkov, K. V. Savostyanov

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CASE OF NON-SEVERE CONGENITAL NEPHROTIC SYNDROME by I. S. Kostushina, T. V. Margieva, T. N. Gusarova, G. T. Yakhyaeva, L. S. Namazova-Baranova, A. A. Pushkov, K. V. Savost'yanov

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Treating TRAPS Syndrome with a Previously Undescribed TNF α Gene Receptor Mutation Successfully with Canakinumab by T. V. Sleptsova, E. I. Alexeeva, K. V. Savostyanov, A. A. Pushkov, T. M. Bzarova, K. B. Isaeva, R. V. Denisova

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Fabry Disease: Symptoms in Children and Teenagers by L. М. Kuzenkova, L. S. Namazova-Baranova, Т. V. Podkletnova, А. K. Gevorkyan, N. D. Vashakmadze, K. V. Savostyanov, V. М. Studenikin, S. А. Pushkov

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CLINICAL CASE OF RARE TYPE V OSTEOGENESIS IMPERFECTA by G. T. Yakhyayeva, T. V. Margieva, L. S. Namazova-Baranova, K. V. Savostyanov, A. A. Pushkov, N. V. Zhurkova, K. V. Zherdev, N. D. Vashakmadze, A. K. Gevorkyan

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Demographic, Clinical and Genetic Characteristics of Child Gaucher Disease Patients in Russia: Pediatric Register Data by G. B. Movsisyan, O. S. Gundobina, L. S. Namazova-Baranova, K. V. Savostyanov, A. N. Pushkov, V. V. Chernikov, N. N. Mazanova, A. M. Romanyuk, V. I. Smirnov

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Managing Children with Gaucher Disease: Modern Clinical Recommendations by A. A. Baranov, L. S. Namazova-Baranova, O. S. Gundobina, E. A. Lukina, A. K. Gevorkyan, K. V. Savostyanov, A. A. Pushkov, E. A. Vishnyova, G. B. Movsisyan

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Experience of the successful treatment with canakinumab of a patient with NLPC4-associated autoinflammatory syndrome with enterocolitis by T. V. Sleptsova, E. I. Alexeeva, K. V. Savost'yanov, A. A. Pushkov, T. M. Bzarova, S. I. Valieva, O. L. Lomakina, R. V. Denisova, K. B. Isaeva, E. G. Chistyakova

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Clinical and Molecular Genetic Features of Autoinflammatory Syndromes in Children by Е. I. Alexeeva, K. V. Savostyanov, Т. V. Sleptsova, А. А. Pushkov, S. I. Valieva, Т. М. Bzarova, K. B. Isaeva, Е. G. Chistyakova, А. М. Chomakhidze, R. V. Denisova, А. G. Nikitin, А. V. Pakhomov

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EXPERIENCE IN APPLICATION OF CANAKINUMAB IN PATIENTS WITH CRYOPYRIN-ASSOCIATED SYNDROME (SYNDROME CINCA/NOMID) by T. V. Sleptsova, E. I. Alexeeva, K. V. Savost'yanov, A. A. Pushkov, A. G. Nikitin, T. M. Bzarova, S. I. Valieva, A. N. Fetisova, A. V. Pakhomov, N. V. Zhurkova, R. V. Denisova, K. B. Isaeva, E. G. Chistyakova

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