Hyperammonemia in Russia Due to Carbonic Anhydrase VA Deficiency Caused by Homozygous Mutation p.Lys185Lys (c.555G>A) of the CA5A Gene
Semenova, Natalia, Marakhonov, Andrey, Ampleeva, Maria, Kurkina, Marina, Baydakova, Galina, Skoblov, Mikhail, Taran, Natalia, Babak, Olga, Shchukina, Ekaterina, Strokova, Tatyana
Published in International journal of molecular sciences (01.12.2022)
Published in International journal of molecular sciences (01.12.2022)
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Journal Article
A novel mutation in the PEX26 gene in a family from Dagestan with members affected by Zellweger spectrum disorder
Semenova, Natalia A., Kurkina, Marina V., Marakhonov, Andrey V., Dadali, Elena L., Taran, Natalia N., Strokova, Tatyana V.
Published in Molecular genetics and metabolism reports (01.06.2021)
Published in Molecular genetics and metabolism reports (01.06.2021)
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Lipid profile of children with glycogen storage disease
Strokova, Tatyana Victorovna, Pavlovskaya, Elena Vyacheslavovna, Zubovich, Andrey Igorevich, Varaeva, Yurgita Ruslanovna, Polenova, Natalia Valerievna, Livansova, Elena Nikolaevna, Bagaeva, Madlena Enverovna, Surkov, Alexander Gennadievich, Kosyura, Svetlana Dmitrievna, Starodubova, Antonina Vladimirovna
Published in Vessel Plus (10.05.2019)
Published in Vessel Plus (10.05.2019)
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Journal Article
METHOD FOR NEUROLEPTANALGESIA
KULIEV ISMAIL YA, STROKOVA TATYANA N, SHARIPOV KAJTPAS SH, DZHEL LYUDMILA L
Year of Publication 23.06.1993
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Year of Publication 23.06.1993
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