Zobrazeno 1 - 10
of 28
pro vyhledávání: '"M. Pasierb"'
Publikováno v:
Atmospheric Measurement Techniques, Vol 16, Pp 4067-4079 (2023)
This paper explores the possibility of using multi-source precipitation estimates for climatological applications. A data-processing algorithm (RainGRS Clim) has been developed to work on precipitation accumulations such as daily or monthly totals, w
Externí odkaz:
https://doaj.org/article/dd8249f0fe07496c8ecc6b23a9420067
Autor:
Job A. J. Verdonschot, Emma L. Robinson, Kiely N. James, Mohamed W. Mohamed, Godelieve R. F. Claes, Kari Casas, Els K. Vanhoutte, Mark R. Hazebroek, Gabriel Kringlen, Michele M. Pasierb, Arthur van denWijngaard, Jan F. C. Glatz, Stephane R. B. Heymans, Ingrid P. C. Krapels, Shareef Nahas, Han G. Brunner, Radek Szklarczyk
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 2, Pp n/a-n/a (2020)
Abstract Background A causal genetic mutation is found in 40% of families with dilated cardiomyopathy (DCM), leaving a large percentage of families genetically unsolved. This prevents adequate counseling and clear recommendations in these families. W
Externí odkaz:
https://doaj.org/article/4c768b28545c4e9c80d7adf8d44f46ec
Akademický článek
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Publikováno v:
Scientific Letters of Rzeszow University of Technology - Mechanics. :401-408
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb1e6b4ede4d310e16d2112b72611701
https://doi.org/10.7862/rm.2017.37
https://doi.org/10.7862/rm.2017.37
Publikováno v:
Echocardiography. 35:1695-1697
Absent pulmonary valve syndrome is a congenital heart defect usually associated with tetralogy of Fallot. Rarely, absent pulmonary valve syndrome can occur independently of tetralogy of Fallot and presents with an intact ventricular septum and a pate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebca53f90d8d941162eeaae5cce0742f
https://doi.org/10.1111/echo.14121
https://doi.org/10.1111/echo.14121
Mutations inPDLIM5are rare in dilated cardiomyopathy but are emerging as potential disease modifiers
Autor:
Kari Casas, Emma L. Robinson, Radek Szklarczyk, Ingrid P.C. Krapels, Gabriel Kringlen, Mohamed W. Mohamed, Kiely N. James, Godelieve R.F. Claes, Shareef Nahas, Jan F. C. Glatz, Els K. Vanhoutte, Michele M. Pasierb, Arthur van den Wijngaard, Stephane Heymans, Job Verdonschot, Han G. Brunner, Mark R. Hazebroek
Publikováno v:
Molecular Genetics & Genomic Medicine, 8, 2
Molecular genetics & genomic medicine, 8(2):e1049. Wiley
Molecular Genetics & Genomic Medicine, 8
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 2, Pp n/a-n/a (2020)
Molecular genetics & genomic medicine, 8(2):e1049. Wiley
Molecular Genetics & Genomic Medicine, 8
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 2, Pp n/a-n/a (2020)
Background A causal genetic mutation is found in 40% of families with dilated cardiomyopathy (DCM), leaving a large percentage of families genetically unsolved. This prevents adequate counseling and clear recommendations in these families. We aim to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4956e352d9f41f1869c143a1c16a309e
https://doi.org/10.1002/mgg3.1049
https://doi.org/10.1002/mgg3.1049
Akademický článek
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Akademický článek
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Publikováno v:
Congenital heart disease. 13(4)
Background Accurate prenatal diagnosis of congenital heart disease (CHD) allows for appropriate delivery and postnatal management. Geographic constraints limit access to fetal cardiology subspecialists. In our approach, general pediatric cardiologist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7bbed93730c45246a4d0379750f50c1
https://pubmed.ncbi.nlm.nih.gov/29938909
https://pubmed.ncbi.nlm.nih.gov/29938909
Autor:
Michele M. Pasierb, Stephen P. Seslar
Publikováno v:
Cardiology in the young. 27(9)
In critically ill children, multi-organ-system disease can influence the choice of antiarrhythmic medication. Intravenous therapy is often necessary. There is a scarcity of paediatric critical-care cases demonstrating the dosing, monitoring, and effi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::877f985bcb904bc510479ac8770a250d
https://pubmed.ncbi.nlm.nih.gov/28797314
https://pubmed.ncbi.nlm.nih.gov/28797314