Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Katelynn M. Ferranti"'
Autor:
Tessa C. Cattermole, McKenna L. Schimmel, Rachel L. Carpenter, Peter W. Callas, Robert Gramling, Daniel J. Bertges, Katelynn M. Ferranti
Publikováno v:
Journal of Vascular Surgery.
Publikováno v:
Journal of Vascular Surgery Cases and Innovative Techniques, Vol 5, Iss 4, Pp 419-422 (2019)
Journal of Vascular Surgery Cases and Innovative Techniques
Journal of Vascular Surgery Cases and Innovative Techniques
Congenital renal arteriovenous fistula (rAVF) is a rare and often underdiagnosed clinical condition. Here, we present a case of a large congenital rAVF in an 81-year-old woman with a right flank bruit and high-output heart failure. The rAVF was succe
Autor:
Amarilis F. Perez, Damek V Spacek, Thomas R. King, David R. Magnan, Lillya K.-L. Wu, Katelynn M. Ferranti, Daniel M. Moy
Publikováno v:
Experimental Dermatology. 19:527-532
Please cite this paper as: The mouse frizzy (fr) and rat ‘hairless’ (frCR) mutations are natural variants of protease serine S1 family member 8 (Prss8). Experimental Dermatology 2010; 19: 527–532. Abstract: We have previously suggested (based o
Publikováno v:
Journal of vascular surgery. 62(4)
The purpose of this study was to evaluate the association of gender with outcomes of peripheral vascular intervention (PVI) for intermittent claudication and critical limb ischemia (CLI).We reviewed 3338 patients (1316 [39%] women) undergoing PVI for
Autor:
Damek V, Spacek, Amarilis F, Perez, Katelynn M, Ferranti, Lillya K-L, Wu, Daniel M, Moy, David R, Magnan, Thomas R, King
Publikováno v:
Experimental dermatology. 19(6)
Please cite this paper as: The mouse frizzy (fr) and rat 'hairless' (fr(CR)) mutations are natural variants of protease serine S1 family member 8 (Prss8). Experimental Dermatology 2010; 19: 527-532. Abstract: We have previously suggested (based on ge