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M Hertz

Showing results (331-340 of 392) with videos related to

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Nanomaterials (Basel, Switzerland)|September 28, 2021
Carbon Quantum Dots Conjugated Rhodium Nanoparticles as Hybrid Multimodal Contrast AgentsGiovanni M Saladino, Nuzhet I Kilic, Bertha Brodin, et al.
Hip International : the Journal of Clinical and Experimental Research on Hip Pathology and Therapy|February 7, 2017
The association between gender and familial prevalence of hip dysplasia in Danish patientsRima El Jashi, Maria B Gustafson, Mette B Jakobsen, et al.
Annals of Emergency Medicine|September 11, 1992
Selective aortic arch perfusion during cardiac arrest: a new resuscitation techniqueJ E Manning, C A Murphy, C M Hertz, et al.
Abdominal Imaging|December 17, 2008
Sealed rupture of abdominal aortic aneurysms: CT features in 6 patients and a review of the literatureS Apter, U Rimon, E Konen, et al.
Physics in Medicine and Biology|July 24, 2018
High-spatial-resolution x-ray fluorescence tomography with spectrally matched nanoparticlesJakob C Larsson, Carmen Vogt, William Vågberg, et al.
The British Journal of Dermatology|May 18, 2011
A founder synonymous COL7A1 mutation in three Danish families with dominant dystrophic epidermolysis bullosa pruriginosa identifies exonic regulatory sequences required for exon 87 splicingC Covaciu, F Grosso, E Pisaneschi, et al.
The British Journal of Radiology|December 1, 2011
CT in the clinical and prognostic evaluation of acute graft-vs-host disease of the gastrointestinal tractA Shimoni, U Rimon, M Hertz, et al.
American Journal of Surgery|August 1, 1993
Comparison of magnetic resonance angiography and contrast arteriography in peripheral arterial stenosisS M Hertz, R A Baum, R S Owen, et al.
Kidney International|March 1, 1993
Mutations in the codon for a conserved arginine-1563 in the COL4A5 collagen gene in Alport syndromeJ Zhou, M C Gregory, J M Hertz, et al.
International Journal of Paediatric Dentistry|June 28, 2011
Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutationDorte Haubek, Hans Gjørup, Lillian G Jensen, et al.
Pageof 40

Showing results (331-340 of 392) with videos related to

Sort By:
Pageof 40
Nanomaterials (Basel, Switzerland)|September 28, 2021
Carbon Quantum Dots Conjugated Rhodium Nanoparticles as Hybrid Multimodal Contrast AgentsGiovanni M Saladino, Nuzhet I Kilic, Bertha Brodin, et al.
Hip International : the Journal of Clinical and Experimental Research on Hip Pathology and Therapy|February 7, 2017
The association between gender and familial prevalence of hip dysplasia in Danish patientsRima El Jashi, Maria B Gustafson, Mette B Jakobsen, et al.
Annals of Emergency Medicine|September 11, 1992
Selective aortic arch perfusion during cardiac arrest: a new resuscitation techniqueJ E Manning, C A Murphy, C M Hertz, et al.
Abdominal Imaging|December 17, 2008
Sealed rupture of abdominal aortic aneurysms: CT features in 6 patients and a review of the literatureS Apter, U Rimon, E Konen, et al.
Physics in Medicine and Biology|July 24, 2018
High-spatial-resolution x-ray fluorescence tomography with spectrally matched nanoparticlesJakob C Larsson, Carmen Vogt, William Vågberg, et al.
The British Journal of Dermatology|May 18, 2011
A founder synonymous COL7A1 mutation in three Danish families with dominant dystrophic epidermolysis bullosa pruriginosa identifies exonic regulatory sequences required for exon 87 splicingC Covaciu, F Grosso, E Pisaneschi, et al.
The British Journal of Radiology|December 1, 2011
CT in the clinical and prognostic evaluation of acute graft-vs-host disease of the gastrointestinal tractA Shimoni, U Rimon, M Hertz, et al.
American Journal of Surgery|August 1, 1993
Comparison of magnetic resonance angiography and contrast arteriography in peripheral arterial stenosisS M Hertz, R A Baum, R S Owen, et al.
Kidney International|March 1, 1993
Mutations in the codon for a conserved arginine-1563 in the COL4A5 collagen gene in Alport syndromeJ Zhou, M C Gregory, J M Hertz, et al.
International Journal of Paediatric Dentistry|June 28, 2011
Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutationDorte Haubek, Hans Gjørup, Lillian G Jensen, et al.
Pageof 40