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European Radiology|November 20, 2002
Cerebral arteriovenous malformations: morphologic evaluation by ultrashort 3D gadolinium-enhanced MR angiographyM Duran, S O Schoenberg, W T C Yuh, et al.
Journal of Inherited Metabolic Disease|October 14, 2000
Isolated and contiguous glycerol kinase gene disorders: a reviewD R Sjarif, J K Ploos van Amstel, M Duran, et al.
Journal of Medical Genetics|June 4, 1998
Molecular study of the rhodopsin gene in retinitis pigmentosa patients in the Basque CountryA I Alvarez, E Arostegui, R Martin, et al.
Tijdschrift Voor Kindergeneeskunde|June 1, 1991
[Molecular genetic aspects of phenylketonuria (PKU)]J C Giltay, A M van Hoef, R de Weger, et al.
Biochemistry|August 27, 2016
Documentation of an Imperative To Improve Methods for Predicting Membrane Protein StabilityBrett M Kroncke, Amanda M Duran, Jeffrey L Mendenhall, et al.
Chest|August 1, 1988
Color Doppler diagnosis of left ventricular pseudoaneurysmJ J Olalla, J A Vazquez de Prada, R M Duran, et al.
Journal of Critical Care|January 10, 2012
Reliability of the validated clinical diagnosis of pneumonia on validated outcomes after intracranial hemorrhageAndrew M Naidech, Storm M Liebling, Isis M Duran, et al.
European Journal of Pediatrics|January 1, 1991
Infantile isolated sulphite oxidase deficiency: report of a case with negative sulphite test and normal sulphate excretionJ M van der Klei-van Moorsel, L M Smit, M Brockstedt, et al.
The Annals of Thoracic Surgery|March 1, 1981
Open mitral commissurotomyJ L Vega, M Fleitas, R Martinez, et al.
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