Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C Hamel

Showing results (111-120 of 291) with videos related to

Pageof 30
Sort By:
Journal Des Maladies Vasculaires|January 1, 1989
[A comparative study of pulsed Doppler versus continuous Doppler technic without spectral analysis in obstetrics]C Hamel-Desnos, J P Henriet, E Lamy, et al.
Journal of Medical Genetics|November 1, 1992
Intestinal pseudo-obstruction in myotonic dystrophyH G Brunner, B C Hamel, P Rieu, et al.
Phlebologie|April 1, 1990
[The value of velocimetric investigation of the uterine arteries in retro-placental hematoma. 3 cases]C Hamel-Desnos, P Desnos, J P Henriet, et al.
Experimental Eye Research|January 27, 1998
The protein truncation test (PTT) as a method of detection for choroideremia mutationsL Beaufrère, S Tuffery, C Hamel, et al.
Journal Des Maladies Vasculaires|January 23, 2014
[Quality standards for ultrasound assessment of the superficial venous system of the lower limbs. Report of the French Society for Vascular Medicine]J-F Auvert, F Chleir, G Coppé, et al.
The Journal of Biological Chemistry|December 29, 1995
Molecular characterization of Golgin-245, a novel Golgi complex protein containing a granin signatureM J Fritzler, C C Lung, J C Hamel, et al.
Chest|January 1, 1981
Extensive aortic dissection from combined-type cystic medial necrosis in a young man without predisposing factorsC B Loeppky, M A Alpert, P C Hamel, et al.
Journal of Medical Genetics|October 1, 1994
Down-Turner syndrome: case report and reviewG J Van Buggenhout, B C Hamel, J C Trommelen, et al.
BMC Medical Research Methodology|October 16, 2020
An evaluation of DistillerSR's machine learning-based prioritization tool for title/abstract screening - impact on reviewer-relevant outcomesC Hamel, S E Kelly, K Thavorn, et al.
Human Mutation|February 6, 1998
Identification of two PAX3 mutations causing Waardenburg syndrome, one within the paired domain (M62V) and the other downstream of the homeodomain (Q282X)F A Hol, M P Geurds, C W Cremers, et al.
Pageof 30

Showing results (111-120 of 291) with videos related to

Sort By:
Pageof 30
Journal Des Maladies Vasculaires|January 1, 1989
[A comparative study of pulsed Doppler versus continuous Doppler technic without spectral analysis in obstetrics]C Hamel-Desnos, J P Henriet, E Lamy, et al.
Journal of Medical Genetics|November 1, 1992
Intestinal pseudo-obstruction in myotonic dystrophyH G Brunner, B C Hamel, P Rieu, et al.
Phlebologie|April 1, 1990
[The value of velocimetric investigation of the uterine arteries in retro-placental hematoma. 3 cases]C Hamel-Desnos, P Desnos, J P Henriet, et al.
Experimental Eye Research|January 27, 1998
The protein truncation test (PTT) as a method of detection for choroideremia mutationsL Beaufrère, S Tuffery, C Hamel, et al.
Journal Des Maladies Vasculaires|January 23, 2014
[Quality standards for ultrasound assessment of the superficial venous system of the lower limbs. Report of the French Society for Vascular Medicine]J-F Auvert, F Chleir, G Coppé, et al.
The Journal of Biological Chemistry|December 29, 1995
Molecular characterization of Golgin-245, a novel Golgi complex protein containing a granin signatureM J Fritzler, C C Lung, J C Hamel, et al.
Chest|January 1, 1981
Extensive aortic dissection from combined-type cystic medial necrosis in a young man without predisposing factorsC B Loeppky, M A Alpert, P C Hamel, et al.
Journal of Medical Genetics|October 1, 1994
Down-Turner syndrome: case report and reviewG J Van Buggenhout, B C Hamel, J C Trommelen, et al.
BMC Medical Research Methodology|October 16, 2020
An evaluation of DistillerSR's machine learning-based prioritization tool for title/abstract screening - impact on reviewer-relevant outcomesC Hamel, S E Kelly, K Thavorn, et al.
Human Mutation|February 6, 1998
Identification of two PAX3 mutations causing Waardenburg syndrome, one within the paired domain (M62V) and the other downstream of the homeodomain (Q282X)F A Hol, M P Geurds, C W Cremers, et al.
Pageof 30