Showing 1 - 20 results of 20 for search 'E.N. Basargina', query time: 0.03s
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DYSPLASIA OF THE HEART CONNECTIVE TISSUE AMONG CHILDREN by E.N. Basargina
Published 2008-01-01
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ALGLUCOSIDASE ALFA — A NEW STAGE IN THE THERAPY OF INFANTILE POMPE DISEASE by E. N. Basargina, E. N. Arkhipova, V. S. Ermolenko
Published 2014-09-01
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INFLUENCE OF THE POLYMORPHISM OF THE RENIN-ANGIOTENSIN SYSTEM GENES ON THE CARDIAC ARRHYTHMIAS IN CHILDREN WITH HYPERTROPHIC CARDIOMYOPATHY by N. A. Berezneva, S. Yu. Nemtseva, O. E. Gromyko, N. S. Aver'yanova, N. D. Vashakhmadze, E. N. Basargina, V. G. Pinelis
Published 2013-05-01
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Clinical Practice Guidelines for delivery of healthcare to patients with Pompe disease by S. S. Nikitin, S. I. Kutsev, E. N. Basargina, S. V. Mikhaylova, E. Yu. Zakharova, V. I. Larionova, S. I. Polyakova, N. P. Kotlukova, E. N. Arkhipova, M. O. Kovalchuk, N. V. Buchinskaya
Published 2016-03-01
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Molecular genetic features of the development of restrictive cardiomyopathy in Russian children by K. V. Savostyanov, E. N. Basargina, E. E. Ryabova, A. A. Pushkov, I. S. Zhanin, E. Yu. Basargina, A. Yu. Alekseeva, L. V. Muraveva, L. A. Gandaeva, A. P. Fisenko
Published 2021-11-01
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EFFECTIVENESS OF MODERN METHODS OF TREATING TYPE I MUCOPOLYSACCHARIDOSIS PATIENTS by L. S. Namazova-Baranova, N. D. Vashakmadze, M. A. Babaikina, E. N. Basargina, N. V. Zhurkova, A. K. Gevorkyan, L. M. Kuzenkova, T. V. Podkletnova, K. V. Zherdev, O. B. Chelpachenko, T. D. Degtyareva
Published 2014-11-01
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Nucleotide sequence variant of the TPM1 gene in a family with different phenotypes of left ventricular non-compaction by M. M. Kudryavtseva, A. V. Kiseleva, R. P. Myasnikov, O. V. Kulikova, A. N. Meshkov, E. A. Mershina, R. K. Angarsky, Е. A. Sotnikova, M. G. Divashuk, A. A. Zharikova, S. N. Koretsky, D. A. Filatova, V. E. Sinitsyn, N. A. Sdvigova, V. I. Barsky, E. N. Basargina, O. M. Drapkina
Published 2023-01-01
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The combination of left ventricular non-compaction and hypertrophic cardiomyopathy in one family with a pathogenic variant in the MYBPC3 gene (rs397516037) by R. P. Myasnikov, A. V. Kulikova, A. N. Meshkov, E. A. Mershina, A. V. Kiseleva, M. V. Klimushina, M. G. Divashuk, O. V. Kurilova, P. S. Pilyus, M. S. Kharlap, S. N. Koretsky, O. M. Larina, V. E. Sinitsyn, L. A. Gandaeva, V. I. Barsky, E. N. Basargina, S. A. Boytsov, O. M. Drapkina
Published 2020-11-01
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Use of Implantable Venous Port Systems in the Treatment of Children with Orphan Diseases (Mucopolysaccharidosis and Pompe Disease): Case Series by M. Yu. Rykov, I. V. Filinov, E. I. Petrov, N. D. Vashakmadze, A. K. Gevorkyan, E. N. Arkhipova, I. V. Sil’nova, E. N. Basargina, N. V. Buchinskaya, A. I. Ivanov, E. A. Isupova, M. M. Kostik, N. A. Abramova, O. V. Kalashnikova, V. G. Chasnyk, A. E. Aleksandrov, D. A. Morozov, V. G. Polyakov
Published 2015-09-01
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New variant of PRDM16 gene nucleotide sequence in a family with various phenotypic manifestations of the non-compacted myocardium by R. P. Myasnikov, A. A. Bukaeva, O. V. Kulikova, A. I. Ershova, A. V. Petukhova, E. D. Zotova, A. N. Meshkov, E. A. Mershina, A. V. Kiseleva, M. G. Divashuk, P. S. Pilyus, M. S. Kharlap, V. M. Mikova, S. N. Koretsky, L. A. Gandaeva, V. E. Sinitsyn, E.. N. Basargina, S. A. Boytsov, E. A. Snigir, A. I. Akinshina, D. A. Kashtanova, V. V. Makarov, V. S. Yudin, O. M. Drapkina
Published 2021-04-01
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