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M Kirchhoff

Showing results (51-60 of 79) with videos related to

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Clinical Genetics|December 5, 2008
Chromosomal deletion unmasking a recessive disease: 22q13 deletion syndrome and metachromatic leukodystrophyA-M Bisgaard, M Kirchhoff, J E Nielsen, et al.
Thrombosis and Haemostasis|November 8, 2005
Acquired Glanzmann's thrombasthenia variant and immune thrombocytopenia in a renal transplant recipient receiving tacrolimusChristian Morath, Till Hoffmann, Elisabeth M Kirchhoff, et al.
European Journal of Medical Genetics|June 12, 2012
Duplication of 7q36.3 encompassing the Sonic Hedgehog (SHH) gene is associated with congenital muscular hypertrophyL Kroeldrup, S Kjaergaard, M Kirchhoff, et al.
Genes and Immunity|January 29, 2011
Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutationL Schejbel, I M Schmidt, M Kirchhoff, et al.
International Journal of Legal Medicine|July 10, 2015
Postmortem computed tomography (PMCT) and autopsy in deadly gunshot wounds--a comparative studyS M Kirchhoff, E F Scaparra, J Grimm, et al.
International Urology and Nephrology|December 25, 2014
The extent of changes in the membranous urethra angle is associated with the outcome of retrourethral transobturator sling procedureIrina Soljanik, Olga Solyanik, Christian G Stief, et al.
World Journal of Urology|June 20, 2012
Morphology and dynamics of the male pelvic floor before and after retrourethral transobturator sling placement: first insight using MRIIrina Soljanik, Ricarda M Bauer, Armin J Becker, et al.
Analytical Biochemistry|October 10, 2012
Quantitative LC-MS/MS analysis of arachidonoyl amino acids in mouse brain with treatment of FAAH inhibitorBingnan Han, Rachel Wright, Aaron M Kirchhoff, et al.
International Journal of Epidemiology|May 26, 1999
Incidence of myocardial infarction in the Danish MONICA population 1982-1991M Kirchhoff, M Davidsen, H Brønnum-Hansen, et al.
Journal of Medical Genetics|June 13, 2009
A new microduplication syndrome encompassing the region of the Miller-Dieker (17p13 deletion) syndromeL Roos, A E Jønch, S Kjaergaard, et al.
Pageof 8

Showing results (51-60 of 79) with videos related to

Sort By:
Pageof 8
Clinical Genetics|December 5, 2008
Chromosomal deletion unmasking a recessive disease: 22q13 deletion syndrome and metachromatic leukodystrophyA-M Bisgaard, M Kirchhoff, J E Nielsen, et al.
Thrombosis and Haemostasis|November 8, 2005
Acquired Glanzmann's thrombasthenia variant and immune thrombocytopenia in a renal transplant recipient receiving tacrolimusChristian Morath, Till Hoffmann, Elisabeth M Kirchhoff, et al.
European Journal of Medical Genetics|June 12, 2012
Duplication of 7q36.3 encompassing the Sonic Hedgehog (SHH) gene is associated with congenital muscular hypertrophyL Kroeldrup, S Kjaergaard, M Kirchhoff, et al.
Genes and Immunity|January 29, 2011
Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutationL Schejbel, I M Schmidt, M Kirchhoff, et al.
International Journal of Legal Medicine|July 10, 2015
Postmortem computed tomography (PMCT) and autopsy in deadly gunshot wounds--a comparative studyS M Kirchhoff, E F Scaparra, J Grimm, et al.
International Urology and Nephrology|December 25, 2014
The extent of changes in the membranous urethra angle is associated with the outcome of retrourethral transobturator sling procedureIrina Soljanik, Olga Solyanik, Christian G Stief, et al.
World Journal of Urology|June 20, 2012
Morphology and dynamics of the male pelvic floor before and after retrourethral transobturator sling placement: first insight using MRIIrina Soljanik, Ricarda M Bauer, Armin J Becker, et al.
Analytical Biochemistry|October 10, 2012
Quantitative LC-MS/MS analysis of arachidonoyl amino acids in mouse brain with treatment of FAAH inhibitorBingnan Han, Rachel Wright, Aaron M Kirchhoff, et al.
International Journal of Epidemiology|May 26, 1999
Incidence of myocardial infarction in the Danish MONICA population 1982-1991M Kirchhoff, M Davidsen, H Brønnum-Hansen, et al.
Journal of Medical Genetics|June 13, 2009
A new microduplication syndrome encompassing the region of the Miller-Dieker (17p13 deletion) syndromeL Roos, A E Jønch, S Kjaergaard, et al.
Pageof 8