Apremilast Pharmacogenomics in Russian Patients with Moderate-to-Severe and Severe Psoriasis

por Verbenko, Dmitry A., Karamova, Arfenya E., Artamonova, Olga G., Deryabin, Dmitry G., Rakitko, Alexander, Chernitsov, Alexandr, Krasnenko, Anna, Elmuratov, Artem, Solomka, Victoria S., Kubanov, Alexey A.
Publicado 2020

Induction of Premature Cell Senescence Stimulated by High Doses of Antioxidants Is Mediated by Endoplasmic Reticulum Stress

por Lyublinskaya, Olga, Kornienko, Julia, Ivanova, Julia, Pugovkina, Natalia, Alekseenko, Larisa, Lyublinskaya, Ekaterina, Tyuryaeva, Irina, Smirnova, Irina, Grinchuk, Tatiana, Shorokhova, Mariia, Krasnenko, Anna, Plotnikov, Nikolay, Nikolsky, Nikolay
Publicado 2021

Compound heterozygous POMGNT1 mutations leading to muscular dystrophy-dystroglycanopathy type A3: a case report

por Borisovna, Kondakova Olga, Yurievna, Krasnenko Anna, Yurievich, Tsukanov Kirill, Igorevna, Klimchuk Olesya, Olegovich, Korostin Dmitriy, Igorevna, Davidova Anna, Timofeevna, Batysheva Tatyana, Vyacheslavovna, Zhurkova Natalia, Ivanovna, Surkova Ekaterina, Alekseevich, Shatalov Peter, Vladimirovich, Ilinsky Valery
Publicado 2019

Liddle syndrome due to a novel mutation in the γ subunit of the epithelial sodium channel (ENaC) in family from Russia: a case report

por Kozina, Anastasiya A., Trofimova, Tatiana A., Okuneva, Elena G., Baryshnikova, Natalia V., Obuhova, Varvara A., Krasnenko, Anna Yu., Tsukanov, Kirill Yu., Klimchuk, Olesya I., Surkova, Ekaterina I., Shatalov, Peter A., Ilinsky, Valery V.
Publicado 2019

A novel MFSD8 mutation in a Russian patient with neuronal ceroid lipofuscinosis type 7: a case report

por Kozina, Anastasiya Aleksandrovna, Okuneva, Elena Grigorievna, Baryshnikova, Natalia Vladimirovna, Krasnenko, Anna Yurievna, Tsukanov, Kirill Yurievich, Klimchuk, Olesya Igorevna, Kondakova, Olga Borisovna, Larionova, Anna Nikolaevna, Batysheva, Tatyana Timofeevna, Surkova, Ekaterina Ivanovna, Shatalov, Peter Alekseevich, Ilinsky, Valery Vladimirovich
Publicado 2018

Two novel PCDH19 mutations in Russian patients with epilepsy with intellectual disability limited to females: a case report

por Kozina, Anastasiya Aleksandrovna, Okuneva, Elena Grigorievna, Baryshnikova, Natalia Vladimirovna, Fedonyuk, Inessa Dmitrievna, Kholin, Alexey Aleksandrovich, Il’ina, Elena Stepanovna, Krasnenko, Anna Yurievna, Stetsenko, Ivan Fedorovich, Plotnikov, Nikolay Alekseevich, Klimchuk, Olesia Igorevna, Surkova, Ekaterina Ivanovna, Ilinsky, Valery Vladimirovich
Publicado 2020

Neuronal ceroid lipofuscinosis in the Russian population: Two novel mutations and the prevalence of heterozygous carriers

por Kozina, Anastasiya A., Okuneva, Elena G., Baryshnikova, Natalia V., Kondakova, Olga B., Nikolaeva, Ekaterina A., Fedoniuk, Inessa D., Mikhailova, Svetlana V., Krasnenko, Anna Y., Stetsenko, Ivan F., Plotnikov, Nikolay A., Klimchuk, Olesia I., Popov, Yaroslav V., Surkova, Ekaterina I., Shatalov, Peter A., Rakitko, Alexander S., Ilinsky, Valery V.
Publicado 2020