Zobrazeno 1 - 10
of 25
pro vyhledávání: '"A. N. Tsygin"'
Autor:
K. V. Savostyanov, A. A. Pushkov, O. A. Shchagina, V. V. Maltseva, E. A. Suleymanov, I. S. Zhanin, N. N. Mazanova, A. P. Fisenko, P. S. Mishakova, A. V. Polyakov, E. V. Balanovska, R. A. Zinchenko, A. N. Tsygin
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Nephropathic cystinosis is a rare autosomal recessive disorder characterized by amino acid cystine accumulation and caused by biallelic mutations in the CTNS gene. The analysis methods are as follows: tandem mass spectrometry to determine the cystine
Externí odkaz:
https://doaj.org/article/667be221ddaa47f189eff65ee120c0c2
Publikováno v:
Вопросы современной педиатрии, Vol 12, Iss 5, Pp 104-107 (2013)
Aim: to investigate sFas-receptor and its ligand, sFas-L, cytochrome C and annexin V as the apoptotic markers in children with CKD to determine the renal cell apoptosis role in the progression of a renal disease. Patients and methods: 68 children wit
Externí odkaz:
https://doaj.org/article/d21788017f0c4e3d9eb7009b8916e896
Autor:
Bella D. Tsintsadze, Klavdiia A. Kazakova, Vladislav V. Chernikov, Andrey P. Fisenko, Anastasiya A. Zhuzhula, Natalia M. Alyabieva, Aleksey N. Tsygin
Publikováno v:
Russian Pediatric Journal. 25:121-127
Introduction. Currently widely adopted benchmarks of normal levels of cystatin in blood and of GFR based on those levels in young children are non-existent. Objective: to determine the content of cystatin C in the blood and the glomerular filtration
Autor:
Anastasiia M. Milovanova, Petr V. Ananin, Tatiana V. Vashurina, Olga I. Zrobok, Alla B. Ryaposova, Alexandr A. Pushkov, Kirill V. Savostyanov, Alexey N. Tsygin
Publikováno v:
Russian Pediatric Journal. 24:381-388
Introduction. Nephrotic syndrome (NS) with an onset in the first year of life is one of the actual problems in pediatric nephrology due to the limited therapeutic options, the ineffectiveness of immunosuppressive therapy, and inevitable progression t
Autor:
Vladislav V. Chernikov, Bella D. Tsintsadze, Andrey P. Fisenko, Klavdiya A. Kazakova, Aleksey N. Tsygin
Publikováno v:
Russian Pediatric Journal. 24:222-230
Introduction. The impact of prematurity on the functional state of the kidneys in infants has not yet been sufficiently studied. Aim. To determine the influence of birth weight and gestational age on the creatinine level in the blood and glomerular f
Autor:
Irina V. Vinyarskaya, Rimma N. Terletskaya, Aleksey N. Tsygin, Andrey P. Fisenko, Elena N. Basargina, Vladislav V Chernikov, Klavdiya A. Kazakova, Elena V. Antonova, Nikolay N. Murashkin, Andrey N. Surkov, Aleksandra M. Chomahidze, Leonid A. Opryatin, Ekkaterina I. Alexeeva
Publikováno v:
Russian Pediatric Journal. 24:106-111
The aim is to identify parents’ (legal representatives’) satisfaction with the quality of medical care provided to their disabled children to improve this type of service further. Materials and methods. A sociological survey was conducted of 506
Autor:
Asmik G. Agaronyan, Olga Komarova, Petr Ananin, T. V. Vashurina, Olga A. Zrobok, Svetlana V. Dmitrienko, Andrey P. Fisenko, Alla B. Ryaposova, Tatyna S. Voznesenskaya, Aleksey N. Tsygin
Publikováno v:
Russian Pediatric Journal. 23:360-364
Introduction. More than half of children with idiopathic nephrotic syndrome have relapsed or become steroid-dependent after the disease’s onset. So far they, require long-term therapy with glucocorticosteroids and/or other immunosuppressive treatme
Autor:
Stefania Drovandi, Beata S. Lipska-Ziętkiewicz, Fatih Ozaltin, Francesco Emma, Bora Gulhan, Olivia Boyer, Agnes Trautmann, Szymon Ziętkiewicz, Hong Xu, Qian Shen, Jia Rao, Korbinian M. Riedhammer, Uwe Heemann, Julia Hoefele, Sarah L. Stenton, Alexey N. Tsygin, Kar-Hui Ng, Svitlana Fomina, Elisa Benetti, Manon Aurelle, Larisa Prikhodina, Anne M. Schijvens, Mansoureh Tabatabaeifar, Maciej Jankowski, Sergey Baiko, Jianhua Mao, Chunyue Feng, Fang Deng, Caroline Rousset-Rouviere, Małgorzata Stańczyk, Irena Bałasz-Chmielewska, Marc Fila, Anne M. Durkan, Tanja Kersnik Levart, Ismail Dursun, Nasrin Esfandiar, Dorothea Haas, Anna Bjerre, Ali Anarat, Marcus R. Benz, Saeed Talebi, Nakysa Hooman, Gema Ariceta, Franz Schaefer, Lina Maria Serna Higuita, Alaleh Gheissari, Nazym Nigmatullina, Marcin Tkaczyk, Halina Borzecka, Radovan Bogdanovic, Sevgi Mir, Thomas Klopstock, Holger Prokisch, Cornelia Kornblum, Cui-Hua Liu, Shu-Zhen Sun, Yang Dong, Xiao-Wen Wang, Jiang-Wei Luan
Publikováno v:
Kidney Int. 102, 592-603 (2022)
Scientia
Scientia
Coenzyme Q10; Mitochondria; Steroid-resistant nephrotic syndrome Coenzima Q10; Mitocondrias; Síndrome nefrótico resistente a los esteroides Coenzim Q10; Mitocondris; Síndrome nefròtic resistent als esteroides Primary Coenzyme Q10 deficiency is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4e1e37391fef1cc876f8e121f4381fe
http://hdl.handle.net/10852/99032
http://hdl.handle.net/10852/99032
Autor:
Stefania Drovandi, Beata S. Lipska-Ziętkiewicz, Fatih Ozaltin, Francesco Emma, Bora Gulhan, Olivia Boyer, Agnes Trautmann, Hong Xu, Qian Shen, Jia Rao, Korbinian M. Riedhammer, Uwe Heemann, Julia Hoefele, Sarah L. Stenton, Alexey N. Tsygin, Kar-Hui Ng, Svitlana Fomina, Elisa Benetti, Manon Aurelle, Larisa Prikhodina, Michiel F. Schreuder, Mansoureh Tabatabaeifar, Maciej Jankowski, Sergey Baiko, Jianhua Mao, Chunyue Feng, Cuihua Liu, Shuzhen Sun, Fang Deng, Xiaowen Wang, Stéphanie Clavé, Małgorzata Stańczyk, Irena Bałasz-Chmielewska, Marc Fila, Anne M. Durkan, Tanja Kersnik Levart, Ismail Dursun, Nasrin Esfandiar, Dorothea Haas, Anna Bjerre, Ali Anarat, Marcus R. Benz, Saeed Talebi, Nakysa Hooman, Gema Ariceta, Franz Schaefer, Lina Maria Serna Higuita, Alaleh Gheissari, Nazym Nigmatullina, Marcin Tkaczyk, Halina Borzecka, Radovan Bogdanovic, Sevgi Mir, Thomas Klopstock, Holger Prokisch, Cornelia Kornblum, Cui-Hua Liu, Shu-Zhen Sun, Yang Dong, Xiao-Wen Wang, Jiang-Wei Luan
Publikováno v:
Kidney International, 102, 3, pp. 604-612
Kidney Int. 102, 604-612 (2022)
Kidney International, 102, 604-612
Kidney Int. 102, 604-612 (2022)
Kidney International, 102, 604-612
Contains fulltext : 283144.pdf (Publisher’s version ) (Open Access) Primary Coenzyme Q10 (CoQ(10)) deficiency is an ultra-rare disorder caused by defects in genes involved in CoQ(10) biosynthesis leading to multidrug-resistant nephrotic syndrome as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b84c27b3e90b69a46a805c20918a32ef
http://hdl.handle.net/10852/100389
http://hdl.handle.net/10852/100389
Autor:
O.A. Zrobok, O. V. Komarova, P.V. Ananin, A.P. Fisenko, T. V. Vashurina, A.G. Timofeeva, A.G. Agaronyan, A. N. Tsygin
Publikováno v:
Nephrology and Dialysis. 22:474-489