Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Adam Golda"'
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 3, Iss C, Pp 11-17 (2015)
Background: Mucopolysaccharidosis type VI (MPS VI) is an autosomal recessive lysosomal disorder caused by a deficient activity of N-acetylgalactosamine-4-sulfatase (ARSB). Pulmonary hypertension (PH) occurs in MPS VI patients and is a marker of bad p
Externí odkaz:
https://doaj.org/article/556d47f18f794cadb813b56530ebd473
Autor:
Aleksander Sinek, Mateusz Mesek, Marek Rojczyk, Jan Juszczyk, Wojciech P. Adamczyk, Jacob Sturdy, Bartłomiej Melka, Adam Golda, Michał Nowok, Ziemowit Ostrowski, Ryszard Białecki
Publikováno v:
Measurement, 2023, Vol. 216, 112904
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c1400f56f78038d91824567e6465d3c
https://repolis.bg.polsl.pl/dlibra/publication/edition/76031/content
https://repolis.bg.polsl.pl/dlibra/publication/edition/76031/content
Autor:
Bartlomiej Melka, Adam Golda, Marek Rojczyk, Ziemowit Ostrowski, Andrzej J. Nowak, Marcin Nowak, Maria Gracka, Ryszard A. Białecki, Wojciech Adamczyk
Publikováno v:
International Journal of Numerical Methods for Heat & Fluid Flow. 30:228-244
Purpose The purpose of this paper is the application of the computational fluid dynamics model simulating the blood flow within the aorta of an eight-year-old patient with Coarctation of Aorta. Design/methodology/approach The numerical model, based o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3c5137e5a26bf53e2fac9bf0e571bd8
https://doi.org/10.1108/hff-04-2019-0279
https://doi.org/10.1108/hff-04-2019-0279
Autor:
Ziemowit Ostrowski, Adam Golda, Maria Gracka, Marek Rojczyk, Wojciech Adamczyk, Andrzej J. Nowak, Ryszard A. Białecki, Bartlomiej Melka
Publikováno v:
Heat and Mass Transfer. 54:2405-2413
In the research, a numerical Computational Fluid Dynamics (CFD) model of the pulsatile blood flow was created and analysed. A real geometry of aorta and its thoracic branches of an 8-year old patient diagnosed with a congenital heart defect – coarc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd7cf7de23c3dd7fdaa090b955bdd55b
https://doi.org/10.1007/s00231-017-2136-y
https://doi.org/10.1007/s00231-017-2136-y
Autor:
Aleksandra Poterala-Hejmo, Anna Lalik, Marcin Pacholczyk, Adam Golda, Sebastian Student, Anna Tylki-Szymańska
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 4913, p 4913 (2020)
International Journal of Molecular Sciences
Volume 21
Issue 14
International Journal of Molecular Sciences
Volume 21
Issue 14
Perturbations of glycosaminoglycan metabolism lead to mucopolysaccharidoses (MPS)&mdash
lysosomal storage diseases. One type of MPS (type VI) is associated with a deficiency of arylsulfatase B (ARSB), for which we previously established a cellul
lysosomal storage diseases. One type of MPS (type VI) is associated with a deficiency of arylsulfatase B (ARSB), for which we previously established a cellul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b00e92959a0ebb6ad969c7769540fd30
https://doi.org/10.3390/ijms21144913
https://doi.org/10.3390/ijms21144913
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 3, Iss C, Pp 11-17 (2015)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Background: Mucopolysaccharidosis type VI (MPS VI) is an autosomal recessive lysosomal disorder caused by a deficient activity of N-acetylgalactosamine-4-sulfatase (ARSB). Pulmonary hypertension (PH) occurs in MPS VI patients and is a marker of bad p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23fb3f8e4a3a55a5cc5ab477f78be74b
Autor:
Vera Malinova, Adam Golda, Loreta Cimbalistiene, Anna Tylki-Szymańska, Agnieszka Jurecka, Elena Voskoboeva, Ekaterina Zakharova, Gulnara Kaldenovna Abdilova, Anna Kulpanovich, Agnieszka Różdżyńska-Świątkowska, Nina Gusina
Publikováno v:
Pediatrics International. 56:520-525
Background The aim of this study was to describe the natural clinical course, incidence and prevalence of mucopolysaccharidosis type VI (MPS VI) in Russia, Kazakhstan, and Central and Eastern Europe. Methods Patients (n = 49) were identified by retri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8963c72bd464da91b27e797467ceb111
https://doi.org/10.1111/ped.12281
https://doi.org/10.1111/ped.12281
Publikováno v:
Metrology and Measurement Systems. 21:111-120
The paper analyzes the phenomenon of heat transfer and its inertia in solids. The influence of this effect on the operation of an integrated circuit is described. The phenomenon is explained using thermal analogy implemented in the Spice environment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a981472a8e8085e23ab5b338d2f6b954
https://doi.org/10.2478/mms-2014-0011
https://doi.org/10.2478/mms-2014-0011
Autor:
Adam Golda, Andrzej Kos
Publikováno v:
Microelectronics Reliability. 53:582-591
The paper presents a method of optimum control of throughput (OCT) of microprocessor (or other processing machine) with taking into account required efficiency, which is taken from operating system, and internal temperature. The optimum performance o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eff9f390546c232befa2ffbdf4e36002
https://doi.org/10.1016/j.microrel.2012.10.014
https://doi.org/10.1016/j.microrel.2012.10.014
Autor:
Ziemowit Ostrowski, Adam Golda, Marek Rojczyk, Wojciech Adamczyk, Andrzej J. Nowak, Bartlomiej Melka
Publikováno v:
Innovations in Biomedical Engineering ISBN: 9783319471532
The paper presents a numerical method of blood flow simulation in two geometries. The first geometry covered the ascending and descending parts of aorta and its main branches in patient with a congenital heart disease - coarctation of aorta (inborn n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f88e31bcac309fa6bdb55ab31a86430a
https://doi.org/10.1007/978-3-319-47154-9_18
https://doi.org/10.1007/978-3-319-47154-9_18