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

F Rivier

Showing results (61-70 of 68) with videos related to

Pageof 7
Sort By:
You have reached the last page of results.This site can display upto 68 results.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 9, 2022
Rare metabolic disease mimicking COL4A1/COL4A2 fetal brain phenotypeT Coste, C Aloui, F Petit, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 2014
[Mitochondrial neurogastrointestinal encephalopathy disease]A Benureau, P Meyer, O Maillet, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|October 14, 2017
Safety, Biodistribution, and Radiation Dosimetry of <sup>68</sup>Ga-OPS202 in Patients with Gastroenteropancreatic Neuroendocrine Tumors: A Prospective Phase I Imaging StudyGuillaume P Nicolas, Seval Beykan, Hakim Bouterfa, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|June 26, 2014
Comparison of somatostatin receptor agonist and antagonist for peptide receptor radionuclide therapy: a pilot studyDamian Wild, Melpomeni Fani, Richard Fischer, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|March 13, 2014
Partial acute transverse myelitis is a predictor of multiple sclerosis in childrenP Meyer, N Leboucq, N Molinari, et al.
Journal of Medical Genetics|August 30, 2008
Refinement of cortical dysgeneses spectrum associated with TUBA1A mutationsN Bahi-Buisson, K Poirier, N Boddaert, et al.
Revue Neurologique|August 20, 2013
[Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]V Humbertclaude, D Hamroun, M-C Picot, et al.
The Journal of Frailty & Aging|November 25, 2016
MACVIA-LR (Fighting Chronic Diseases for Active and Healthy Ageing in Languedoc-Roussillon): A Success Story of the European Innovation Partnership on Active and Healthy AgeingJ Bousquet, R Bourret, T Camuzat, et al.
Pageof 7

Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 9, 2022
Rare metabolic disease mimicking COL4A1/COL4A2 fetal brain phenotypeT Coste, C Aloui, F Petit, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 2014
[Mitochondrial neurogastrointestinal encephalopathy disease]A Benureau, P Meyer, O Maillet, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|October 14, 2017
Safety, Biodistribution, and Radiation Dosimetry of <sup>68</sup>Ga-OPS202 in Patients with Gastroenteropancreatic Neuroendocrine Tumors: A Prospective Phase I Imaging StudyGuillaume P Nicolas, Seval Beykan, Hakim Bouterfa, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|June 26, 2014
Comparison of somatostatin receptor agonist and antagonist for peptide receptor radionuclide therapy: a pilot studyDamian Wild, Melpomeni Fani, Richard Fischer, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|March 13, 2014
Partial acute transverse myelitis is a predictor of multiple sclerosis in childrenP Meyer, N Leboucq, N Molinari, et al.
Journal of Medical Genetics|August 30, 2008
Refinement of cortical dysgeneses spectrum associated with TUBA1A mutationsN Bahi-Buisson, K Poirier, N Boddaert, et al.
Revue Neurologique|August 20, 2013
[Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]V Humbertclaude, D Hamroun, M-C Picot, et al.
The Journal of Frailty & Aging|November 25, 2016
MACVIA-LR (Fighting Chronic Diseases for Active and Healthy Ageing in Languedoc-Roussillon): A Success Story of the European Innovation Partnership on Active and Healthy AgeingJ Bousquet, R Bourret, T Camuzat, et al.
Pageof 7