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pro vyhledávání: '"M. L. Watson"'
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Autor:
Zickler, Antje M.1,2,3 (AUTHOR) antje.zickler@ki.se, Liang, Xiuming1,2,3,4 (AUTHOR) xiuming.liang@ki.se, Gupta, Dhanu1,2,5 (AUTHOR), Mamand, Doste R.1,2,3,6 (AUTHOR), De Luca, Mariacristina7,8 (AUTHOR), Corso, Giulia1,2,9 (AUTHOR), Errichelli, Lorenzo7 (AUTHOR), Hean, Justin7 (AUTHOR), Sen, Titash7,10 (AUTHOR), Elsharkasy, Omnia M.1,2,3 (AUTHOR), Kamei, Noriyasu1,2,11 (AUTHOR), Niu, Zheyu1,2,12 (AUTHOR), Zhou, Guannan1,2,13 (AUTHOR), Zhou, Houze1,2,3 (AUTHOR), Roudi, Samantha1,2,3 (AUTHOR), Wiklander, Oscar P. B.1,3,6 (AUTHOR), Görgens, André1,2,3,14 (AUTHOR), Nordin, Joel Z.1,3,15 (AUTHOR), Castilla‐Llorente, Virginia7,16 (AUTHOR), EL Andaloussi, Samir1,2,3 (AUTHOR) samir.el-andaloussi@ki.se
Publikováno v:
Advanced Science. 11/13/2024, Vol. 11 Issue 42, p1-16. 16p.
Seven novel mutations of the PKD2 gene in families with autosomal dominant polycystic kidney disease
Autor:
José L. San Millán, M. L. Watson, D Telleria, M Viribay, Peter C. Harris, Celia Badenas, Roser Torra, Alejandro Darnell
Publikováno v:
Kidney International. 56:28-33
Seven novel mutations of the PKD2 gene in families with autosomal dominant polycystic kidney disease. Background Autosomal dominant polycystic kidney disease (ADPKD) is genetically heterogeneous, with at least three chromosomal loci accounting for th
Autor:
S E Pound, Peter C. Harris, M L Watson, Anna Maria Frischauf, S. Thomas, P M Pignatelli, A F Wright, A. Snarey, A M Macnicol
Publikováno v:
Journal of Medical Genetics. 32:208-212
Haplotype analysis was performed in 35 autosomal dominant polycystic kidney disease (ADPKD) families typed with 13 markers close to the PKD1 locus. The identification of recombinants close to the PKD1 gene on chromosome 16p indicates that PKD1 lies b
Autor:
Novacescu, Dorin1,2 (AUTHOR) novacescu.dorin@umft.ro, Latcu, Silviu Constantin3,4,5 (AUTHOR) daminescu75@gmail.com, Raica, Marius1,2 (AUTHOR) marius.raica@umft.ro, Baderca, Flavia1,2 (AUTHOR) baderca.flavia@umft.ro, Dumitru, Cristina-Stefania1,2 (AUTHOR) cristina-stefania.dumitru@umft.ro, Daminescu, Liviu4 (AUTHOR) razvan.bardan@umft.ro, Bardan, Razvan4,5 (AUTHOR) cumpanas.alin@umft.ro, Dema, Vlad3,4,5 (AUTHOR) alexei.croitor@umft.ro, Croitor, Alexei3,4,5 (AUTHOR), Cut, Talida Georgiana6,7 (AUTHOR) talida.cut@umft.ro, Cumpanas, Alin Adrian4,5 (AUTHOR)
Publikováno v:
Journal of Clinical Medicine. Jul2024, Vol. 13 Issue 14, p4188. 25p.
Publikováno v:
Acute medicine. 5(2)
Native renal artery stenosis resulting in hypertensive encephalopathy is exceptionally rare, with only 3 previous case reports in adults. We report such a case in a previously well 20 year old female.
Publikováno v:
Journal of Magnetism and Magnetic Materials. 114:L230-L234
‘Giant’ magnetoresistance ratios have been measured at room temperature in as-deposited, single layer Co-Ag alloy thin films sputtered from a composite target. The effect has been observed over a broad range of Co concentrations (from 0.25 to 0.5
Publikováno v:
Kidney International. 41(1):206-210
Effects of angiotensin converting enzyme inhibition in adult polycystic kidney disease. The pathogenesis of hypertension in autosomal-dominant polycystic kidney disease (ADPKD) is unclear, but increased activity of the renin-angiotensin system may co