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M Winter

Showing results (731-740 of 1,268) with videos related to

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Lancet (London, England)|July 31, 2001
Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromesX Zhou, H Hampel, H Thiele, et al.
The American Journal of Occupational Therapy : Official Publication of the American Occupational Therapy Association|March 7, 2012
Rater reliability and rater effects of the Safe Driving Behavior MeasureSherrilene Classen, Pey-Shan Wen, Craig A Velozo, et al.
Journal of Applied Clinical Medical Physics|November 28, 2025
Dosimetric evaluation of magnetic resonance imaging based synthetic computed tomography for head and neck photon and proton therapyMarte Kåstad Høiskar, René M Winter, Natalie Hornik, et al.
International Journal of Cardiology|February 25, 2009
Mechanisms for cardiac output augmentation in patients with a systemic right ventricleMichiel M Winter, Mart N van der Plas, Berto J Bouma, et al.
Journal of Medical Genetics|September 1, 1996
A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricansD Wilkes, P Rutland, L J Pulleyn, et al.
Contrast Media & Molecular Imaging|June 30, 2010
Assessment of tumor angiogenesis: dynamic contrast-enhanced MRI with paramagnetic nanoparticles compared with Gd-DTPA in a rabbit Vx-2 tumor modelAndrea Kassner, Rebecca E Thornhill, Fang Liu, et al.
Letters in Applied Microbiology|May 9, 2009
Establishing relative release kinetics of faecal indicator organisms from different faecal matricesC J Hodgson, N Bulmer, D R Chadwick, et al.
Critical Care Medicine|December 1, 1999
Hypoxemia after coronary bypass surgery modeled by resistance to oxygen diffusionS Andreassen, S E Rees, S Kjaergaard, et al.
Current Topics in Medicinal Chemistry|May 29, 2003
The role of absorption, distribution, metabolism, excretion and toxicity in drug discoveryJing Lin, Diana C Sahakian, Sonia M F de Morais, et al.
Human Molecular Genetics|September 4, 2003
Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseasesH Annika Siitonen, Outi Kopra, Helena Kääriäinen, et al.
Pageof 127

Showing results (731-740 of 1,268) with videos related to

Sort By:
Pageof 127
Lancet (London, England)|July 31, 2001
Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromesX Zhou, H Hampel, H Thiele, et al.
The American Journal of Occupational Therapy : Official Publication of the American Occupational Therapy Association|March 7, 2012
Rater reliability and rater effects of the Safe Driving Behavior MeasureSherrilene Classen, Pey-Shan Wen, Craig A Velozo, et al.
Journal of Applied Clinical Medical Physics|November 28, 2025
Dosimetric evaluation of magnetic resonance imaging based synthetic computed tomography for head and neck photon and proton therapyMarte Kåstad Høiskar, René M Winter, Natalie Hornik, et al.
International Journal of Cardiology|February 25, 2009
Mechanisms for cardiac output augmentation in patients with a systemic right ventricleMichiel M Winter, Mart N van der Plas, Berto J Bouma, et al.
Journal of Medical Genetics|September 1, 1996
A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricansD Wilkes, P Rutland, L J Pulleyn, et al.
Contrast Media & Molecular Imaging|June 30, 2010
Assessment of tumor angiogenesis: dynamic contrast-enhanced MRI with paramagnetic nanoparticles compared with Gd-DTPA in a rabbit Vx-2 tumor modelAndrea Kassner, Rebecca E Thornhill, Fang Liu, et al.
Letters in Applied Microbiology|May 9, 2009
Establishing relative release kinetics of faecal indicator organisms from different faecal matricesC J Hodgson, N Bulmer, D R Chadwick, et al.
Critical Care Medicine|December 1, 1999
Hypoxemia after coronary bypass surgery modeled by resistance to oxygen diffusionS Andreassen, S E Rees, S Kjaergaard, et al.
Current Topics in Medicinal Chemistry|May 29, 2003
The role of absorption, distribution, metabolism, excretion and toxicity in drug discoveryJing Lin, Diana C Sahakian, Sonia M F de Morais, et al.
Human Molecular Genetics|September 4, 2003
Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseasesH Annika Siitonen, Outi Kopra, Helena Kääriäinen, et al.
Pageof 127