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Izzet Yavuz

Showing results (21-30 of 31) with videos related to

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Archivos Argentinos De Pediatria|March 21, 2018
[Isotretinoin embryopathy: An entity that can be avoided]Francisco Cammarata-Scalisi, Dairelis Nieves, Andrea Avendaño, et al.
Journal of Clinical and Experimental Dentistry|April 20, 2018
The Evaluation of Root Fracture with Cone Beam Computed Tomography (CBCT): An Epidemiological StudyMehmet-Sinan Doğan, Michele Callea, Lindawati S Kusdhany, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|January 21, 2004
Increased P wave dispersion and maximum P wave duration after hemodialysisUgur K Tezcan, Basri Amasyali, Ilknur Can, et al.
Nephrology (Carlton, Vic.)|March 21, 2007
Effect of antihypertensive agents on plasma adiponectin levels in hypertensive patients with metabolic syndromeMahmut I Yilmaz, Alper Sonmez, Kayser Caglar, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 29, 2002
Cumulative prior dose of cisplatin as a cause of the nephrotoxicity of high-dose chemotherapy followed by autologous stem-cell transplantationKayser Caglar, Can Kinalp, Fikret Arpaci, et al.
Journal of Nephrology|March 30, 2010
Differences in ischemia-modified albumin levels between end stage renal disease patients and the normal populationSuleyman Turedi, Orhan Cinar, Izzet Yavuz, et al.
Archivos Argentinos De Pediatria|November 1, 2017
[Clinical and molecular study in a family with cleidocranial dysplasia]Michele Callea, Fabiana Fattori, Enrico S Bertini, et al.
Archivos Argentinos De Pediatria|January 19, 2017
[Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia]Michele Callea, Francisco Cammarata-Scalisi, Colin E Willoughby, et al.
Investigacion Clinica|June 26, 2018
A c.3037G>A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotypeMichele Callea, Colin Eric Willoughby, Francisco Camarata-Scalisi, et al.
Life (Basel, Switzerland)|June 24, 2022
Anti-Inflammatory, Antioxidant, and Anti-Atherosclerotic Effects of Natural Supplements on Patients with FMF-Related AA Amyloidosis: A Non-Randomized 24-Week Open-Label Interventional StudyMicol Romano, Facundo Garcia-Bournissen, David Piskin, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Archivos Argentinos De Pediatria|March 21, 2018
[Isotretinoin embryopathy: An entity that can be avoided]Francisco Cammarata-Scalisi, Dairelis Nieves, Andrea Avendaño, et al.
Journal of Clinical and Experimental Dentistry|April 20, 2018
The Evaluation of Root Fracture with Cone Beam Computed Tomography (CBCT): An Epidemiological StudyMehmet-Sinan Doğan, Michele Callea, Lindawati S Kusdhany, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|January 21, 2004
Increased P wave dispersion and maximum P wave duration after hemodialysisUgur K Tezcan, Basri Amasyali, Ilknur Can, et al.
Nephrology (Carlton, Vic.)|March 21, 2007
Effect of antihypertensive agents on plasma adiponectin levels in hypertensive patients with metabolic syndromeMahmut I Yilmaz, Alper Sonmez, Kayser Caglar, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 29, 2002
Cumulative prior dose of cisplatin as a cause of the nephrotoxicity of high-dose chemotherapy followed by autologous stem-cell transplantationKayser Caglar, Can Kinalp, Fikret Arpaci, et al.
Journal of Nephrology|March 30, 2010
Differences in ischemia-modified albumin levels between end stage renal disease patients and the normal populationSuleyman Turedi, Orhan Cinar, Izzet Yavuz, et al.
Archivos Argentinos De Pediatria|November 1, 2017
[Clinical and molecular study in a family with cleidocranial dysplasia]Michele Callea, Fabiana Fattori, Enrico S Bertini, et al.
Archivos Argentinos De Pediatria|January 19, 2017
[Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia]Michele Callea, Francisco Cammarata-Scalisi, Colin E Willoughby, et al.
Investigacion Clinica|June 26, 2018
A c.3037G>A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotypeMichele Callea, Colin Eric Willoughby, Francisco Camarata-Scalisi, et al.
Life (Basel, Switzerland)|June 24, 2022
Anti-Inflammatory, Antioxidant, and Anti-Atherosclerotic Effects of Natural Supplements on Patients with FMF-Related AA Amyloidosis: A Non-Randomized 24-Week Open-Label Interventional StudyMicol Romano, Facundo Garcia-Bournissen, David Piskin, et al.
Pageof 4