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D Christmann

Showing results (131-140 of 137) with videos related to

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International Journal of Clinical Practice|May 16, 2008
Value of (18)F-FDG-PET/CT in patients with fever of unknown origin and unexplained prolonged inflammatory syndrome: a single centre analysis experienceL Federici, C Blondet, A Imperiale, et al.
Clinical Genetics|September 10, 2010
Osteosclerotic bone dysplasia in siblings with a Fam20C mutationMelanie Fradin, C Stoetzel, J Muller, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|December 27, 2016
VISLISI trial, a prospective clinical study allowing identification of a new metalloprotease and putative virulence factor from Staphylococcus lugdunensisX Argemi, G Prévost, P Riegel, et al.
Clinical Genetics|April 27, 2011
Hippocampal dysgenesis and variable neuropsychiatric phenotypes in patients with Bardet-Biedl syndrome underline complex CNS impact of primary ciliaV Bennouna-Greene, S Kremer, C Stoetzel, et al.
European Journal of Cancer|January 1, 1980
Adjuvant chemotherapy with chlorambucil and 5-fluorouracil in primary breast cancer (Cooperative Study Heidelberg)M Kaufmann, D V Fournier, H Sievers, et al.
Molecular Syndromology|December 23, 2011
Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent PolydactylyE Schaefer, A Zaloszyc, J Lauer, et al.
Basic Research in Cardiology|August 23, 2025
Calcific aortic valve disease augments vesicular microRNA-145-5p to regulate the calcification of valvular interstitial cells via cellular crosstalkP R Goody, D Christmann, D Goody, et al.
Pageof 14

Showing results (131-140 of 137) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 137 results.
International Journal of Clinical Practice|May 16, 2008
Value of (18)F-FDG-PET/CT in patients with fever of unknown origin and unexplained prolonged inflammatory syndrome: a single centre analysis experienceL Federici, C Blondet, A Imperiale, et al.
Clinical Genetics|September 10, 2010
Osteosclerotic bone dysplasia in siblings with a Fam20C mutationMelanie Fradin, C Stoetzel, J Muller, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|December 27, 2016
VISLISI trial, a prospective clinical study allowing identification of a new metalloprotease and putative virulence factor from Staphylococcus lugdunensisX Argemi, G Prévost, P Riegel, et al.
Clinical Genetics|April 27, 2011
Hippocampal dysgenesis and variable neuropsychiatric phenotypes in patients with Bardet-Biedl syndrome underline complex CNS impact of primary ciliaV Bennouna-Greene, S Kremer, C Stoetzel, et al.
European Journal of Cancer|January 1, 1980
Adjuvant chemotherapy with chlorambucil and 5-fluorouracil in primary breast cancer (Cooperative Study Heidelberg)M Kaufmann, D V Fournier, H Sievers, et al.
Molecular Syndromology|December 23, 2011
Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent PolydactylyE Schaefer, A Zaloszyc, J Lauer, et al.
Basic Research in Cardiology|August 23, 2025
Calcific aortic valve disease augments vesicular microRNA-145-5p to regulate the calcification of valvular interstitial cells via cellular crosstalkP R Goody, D Christmann, D Goody, et al.
Pageof 14