1. A kinetic assay of total lipase activity for detecting lysosomal acid lipase deficiency (LAL‐D) and the molecular characterization of 18 LAL‐D patients from Russia. Issue 1 (3rd June 2019) Authors: Mayanskiy, Nikolay; Brzhozovskaya, Ekaterina; Pushkov, Alexander; Strokova, Tatiana; Vlasov, Nikolay; Surkov, Andrej; Gundobina, Olga; Savostianov, Kirill Journal: JIMD reports Issue: Volume 48:Issue 1(2019) Page Start: 75 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. GP126 Large deletions in DMD gene is the most prevalence mutation in russian children with duchenne muscular dystrophy. (June 2019) Authors: Savostyanov, Kirill; Pushkov, Alexander; Kuzenkova, Ludmila; Zhurkova, Natalya; Nikitin, Alexey; Kurenkov, Alexey; Bursagova, Bella; Trufanov, Sergey Journal: Archives of disease in childhood Issue: Volume 104:(2019)Supplement 3 Page Start: A81 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. GP5 The immunogenetics and risk factors of pollinosis among russian children. case-control study. (June 2019) Authors: Levina, Julia; Namazova-Baranova, Leyla; Savostyanov, Kirill; Pushkov, Alexander; Burdennyy, Alexey; Alekseeva, Anna; Efendieva, Kamilla; Vishneva, Elena Journal: Archives of disease in childhood Issue: Volume 104:(2019)Supplement 3 Page Start: A31 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. GP76 Experience in treatment of bladder exstrophy in newborn girl with apert syndrome. (June 2019) Authors: Gurskaya, Alexandra; Mokrushina, Olga; Nakovkin, Oleg; Sulavko, Maria; Akhmedova, Dinara; Tarzyan, Aram; Zhurkova, Natalya; Savostyanov, Kirill; Pushkov, Alexander; Sladkov, Dmitry Journal: Archives of disease in childhood Issue: Volume 104:(2019)Supplement 3 Page Start: A60 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. P190 Complement system genes mutation spectrum in russian children with atypical hemolytic uremic syndrome. (6th June 2017) Authors: Tsygin, Alexey; Ananin, Petr; Mazo, Alexandra; Komarova, Olga; Vashurina, Tatiana; Zrobok, Olga; Pushkov, Alexander; Savostianov, Kirill Journal: Archives of disease in childhood Issue: Volume 102(2017)Supplement 2 Page Start: A107 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗