Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Ludmila Kuzenkova"'
Autor:
Kirill Savostyanov, Alexander Pushkov, Ilya Zhanin, Natalya Mazanova, Alexander Pakhomov, Elena Trufanova, Alina Alexeeva, Dmitry Sladkov, Ludmila Kuzenkova, Aliy Asanov, Andrey Fisenko
Publikováno v:
Genes, Vol 14, Iss 11, p 2016 (2023)
Background: Fabry disease (FD) is a rare hereditary multisystem disease caused by variants of the GLA gene. Determination of GLA gene variants and identification of genotype–phenotype correlations allow us to explain the features of FD associated w
Externí odkaz:
https://doaj.org/article/6cc5c3a850d24331b3e5e73aab29b6b6
Publikováno v:
L.O. Badalyan Neurological Journal. 2:22-28
Introduction. Autism is a disorder characterized by social interaction disorders, social-emotional reciprocity, responses to other people’s emotions, social use of speech skills, lack of modulations of behavior under the social situation, and limit
Autor:
Alexey Kurenkov, Ludmila Kuzenkova, Sergey Trufanov, Alexey Nikitin, Alexander Pushkov, Kirill Savostyanov, Natalya Zhurkova, Bella Bursagova
Publikováno v:
Abstracts.
Background and objectives Duchenne muscular dystrophy (DMD) is a rare muscle disorder inherited by X-linked recessive type and affecting approximately 1 in 3,500 male births worldwide. Patients and methods The study included 63 boys, aged from 6 mont
Autor:
Olga V. Kozhevnikova, Ludmila Kuzenkova, Alexander A. Buksh, Tatyana Podkletnova, Liliya A. Osipova
Publikováno v:
Molecular Genetics and Metabolism. 129:S124
Autor:
Natalia V. Zhurkova, Lolita Pak, Alexander Pushkov, Ludmila Kuzenkova, Kirill Savostyanov, Tatyana Podkletnova, Andrey P. Fisenko, Alexander Pakhomov, Alina Yu. Alexeeva, Sergey Trufanov
Publikováno v:
Molecular Genetics and Metabolism. 129:S133
Autor:
Ludmila Kuzenkova, Sofya Demura, Nataliya Zhurkova, Anahit Gevorkyan, Nato Vashakmadze, Tatyana Podkletnova, Leyla Namazova-Baranova, Mariia Fadeeva
Publikováno v:
Molecular Genetics and Metabolism. 126:S147-S148
Autor:
Elena Vishneva, Anait K. Gevorkyan, Ludmila Kuzenkova, Liliya Selimzyanova, Nato Vashakmadze, Leyla Namazova-Baranova
Publikováno v:
Paediatric Respiratory Physiology and Sleep.
Background: mucopolysaccharidoses are rare genetic storage diseases with deficient activity of lysosomal enzymes. Patients with mucopolysaccharidoses have multiorgan pathology, including respiratory system impairment. It is important to complex eluci
Autor:
Ludmila Kuzenkova, Tatyana Podkletnova, Liliya A. Osipova, Nato M Vashakmadze, L.S. Namazova-Baranova, Anait K. Gevorkyan, Galina V. Kuznetsova
Publikováno v:
Posters.
Subdural hematomas are most common in infants and elderly adults and result from bridging veins’ tears. Subdural haemorrhage has been described in several neurometabolic diseases with cerebral atrophy, including MPS II and IIIB. Few reports describ
Autor:
Nataliya Zhurkova, Ludmila Kuzenkova, Tatiana Privalova, Anastasia Rykunova, Anahit Gevorkyan, Elena Komarova, Nato Vashakmadze, Leyla Namazova-Baranova, Tatyana Podkletnova
Publikováno v:
Molecular Genetics and Metabolism. 126:S148
Autor:
Ludmila Kuzenkova, Natalia V. Zhurkova, Kirill Savostyanov, Alexandr Andreevich Pushkov, Evgeny Leonidovich Penkov, Nato Vashakmadze, Tatiana V. Podkletnova
Publikováno v:
Molecular Genetics and Metabolism. 126:S156