Zobrazeno 1 - 10
of 80
pro vyhledávání: '"V L, Emanuel"'
Publikováno v:
Нервно-мышечные болезни, Vol 12, Iss 3, Pp 36-44 (2022)
Background. Proximal spinal muscular atrophy 5q (5q‑SMA) is one of the most common neuromuscular diseases, which is caused by mutations of the SMN1 gene. Despite the fact that most studies consider SMN1 “deletion” as the most common cause of 5q
Externí odkaz:
https://doaj.org/article/256111deb28f4884aebec07f19989666
Autor:
A. A. Musaelyan, A. L. Akopov, S. V. Lapin, V. D. Nazarov, D. I. Fillipov, V. L. Emanuel, S. V. Orlov
Publikováno v:
Успехи молекулярной онкологии, Vol 8, Iss 3, Pp 34-43 (2021)
Immune checkpoint inhibitors (ICIs) alone or in combination with chemotherapy have become one of the key approaches in the treatment of patients with advanced non-small cell lung cancer (NSCLC). Evaluation of level of PD-L1 (ligand of the programmed
Externí odkaz:
https://doaj.org/article/62229f8a1c4346e2b9b5224260d6307e
Publikováno v:
Антибиотики и Химиотерапия, Vol 66, Iss 7-8, Pp 30-37 (2021)
Relevance: The two systems for determining the susceptibility of bacteria to antimicrobial drugs, CLSI and EUCAST, are recommended for use in the global system of epidemiological surveillance of antimicrobial resistance of the World Health Organizati
Externí odkaz:
https://doaj.org/article/20ed5a2a1207497dbb5199f6c993fce9
Publikováno v:
Vestnik Urologii, Vol 9, Iss 3, Pp 44-51 (2021)
Introduction. Urolithiasis is a multifactorial recurrent disease, unevenly spread throughout the world and characterizedby the formation of urinary stones of various chemical compositions, depending on pathogenesis, etiological, and epidemiological r
Externí odkaz:
https://doaj.org/article/83ea79da79e740a39d378da47eb6b4a7
Autor:
A. A. Musaelyan, V. D. Nazarov, A. S. Budnikova, S. V. Lapin, S. L. Vorobyev, V. L. Emanuel, A. A. Zakharenko, S. V. Orlov
Publikováno v:
Успехи молекулярной онкологии, Vol 8, Iss 2, Pp 52-59 (2021)
Background. Microsatellites are short tandem nucleotide repeats, the change in length of which plays a key roles in the pathogenesis of various malignant neoplasms. This change is called microsatellite instability. It is caused by aberrations in the
Externí odkaz:
https://doaj.org/article/15d7de81cc7f44ec97b28e0759d59dc7
Autor:
M. S. Vonsky, A. L. Runov, T. S. Gorjachaya, A. M. Koltsova, E. V. Kurchakova, V. D. Nazarov, S. V. Lapin, A. V. Mazing, V. L. Emanuel
Publikováno v:
Measurement Standards. Reference Materials. 19:5-17
Cancer is the leading cause of death in the world. The development of oncopathology is closely related to various changes in the genetic material that occur in malignantly transformed cells. Medical decision-making requires a clear differentiation be
Autor:
N. A. Verlov, L. S. Gulina, V. S. Burdakov, I. S. Kulakov, S. B. Landa, A. A. Bogdanov, A. V. Yakovleva, V. L. Emanuel
Publikováno v:
Medical alphabet. :18-22
Introduction. Experimental model of intraperitoneal injection of sodium oxalate is one of the most promising and practical models of oxalate urolithiasis in rodents.Purpose of the study. To describe the urolithiasis progression in experimental animal
Autor:
C. C. Cherebillo, V. D. Nazarov, C. V. Lapin, N. A. Totolyan, E. V. Bubnova, G. S. Makshakov, A. V. Mazing, N. V. Shuleshova, Y. M. Kiryanov, V. L. Emanuel
Publikováno v:
Russian neurological journal. 28:13-24
Introduction. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is common variant of small vessel disease. Determination of neuroimaging markers have already contributed at an early stage to the more
Publikováno v:
Medical alphabet. :7-11
In accordance with GOST R ISO 15189–2015 ‘Medical laboratories. Particular requirements for quality and competence’ for the report on the values of the measured value in the patient’s samples, the laboratory must determine and use the measure
Autor:
M. Yu. Pervakova, A. L. Chudinov, S. V. Lapin, I. B. Belyaeva, V. I. Mazurov, T. V. Blinova, E. A. Surkova, V. L. Emanuel, O. V. Inamova
Publikováno v:
Научно-практическая ревматология, Vol 55, Iss 2, Pp 164-168 (2017)
α1-Antitrypsin (α1-AT) deficiency is a common genetic disorder characterized by low serum α1-AT levels and a clinical manifestation of pulmonary emphysema and liver disease. In addition to its classical manifestations, α1-AT deficiency frequently
Externí odkaz:
https://doaj.org/article/89721449a6d24e1ab71aeb3ed5f352c4