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 Brunelle

Showing results (201-210 of 244) with videos related to

Pageof 25
Sort By:
Journal of Neurosurgery|February 6, 1998
Hydrocephalus and craniosynostosisG Cinalli, C Sainte-Rose, E M Kollar, et al.
Annales D'Endocrinologie|April 6, 1999
Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasiaJ C Fournet, V Verkarre, P De Lonlay, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 1, 1995
[Chronic septic granulomatosis revealed by neonatal pulmonary aspergillosis]R Mouy, J C Ropert, J Donadieu, et al.
Pediatric Radiology|August 21, 2001
Pancreatic arterial calcium stimulation in the diagnosis and localisation of persistent hyperinsulinemic hypoglycaemia of infancyV Chigot, P De Lonlay, M C Nassogne, et al.
AJNR. American Journal of Neuroradiology|May 30, 2015
Choroid Plexus Neoplasms: Toward a Distinction between Carcinoma and Papilloma Using Arterial Spin-LabelingV Dangouloff-Ros, D Grevent, M Pagès, et al.
Journal of Medical Genetics|May 6, 2014
Brain imaging in mitochondrial respiratory chain deficiency: combination of brain MRI features as a useful tool for genotype/phenotype correlationsM Bricout, D Grévent, A S Lebre, et al.
Pediatric Radiology|December 2, 2000
Intracranial venous anomalies associated with atretic cephalocoelesF Brunelle, J Baraton, D Renier, et al.
Clinical Genetics|September 29, 2009
Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression burstsF Molinari, A Kaminska, G Fiermonte, et al.
Hormone Research|July 15, 2000
Loss of imprinted genes and paternal SUR1 mutations lead to focal form of congenital hyperinsulinismJ C Fournet, C Mayaud, P de Lonlay, et al.
Revue Neurologique|April 29, 2014
[Aspect of brain MRI in mitochondrial respiratory chain deficiency. A diagnostic algorithm of the most common mitochondrial genetic mutations]M Devaux-Bricout, D Grévent, A-S Lebre, et al.
Pageof 25

Showing results (201-210 of 244) with videos related to

Sort By:
Pageof 25
Journal of Neurosurgery|February 6, 1998
Hydrocephalus and craniosynostosisG Cinalli, C Sainte-Rose, E M Kollar, et al.
Annales D'Endocrinologie|April 6, 1999
Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasiaJ C Fournet, V Verkarre, P De Lonlay, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 1, 1995
[Chronic septic granulomatosis revealed by neonatal pulmonary aspergillosis]R Mouy, J C Ropert, J Donadieu, et al.
Pediatric Radiology|August 21, 2001
Pancreatic arterial calcium stimulation in the diagnosis and localisation of persistent hyperinsulinemic hypoglycaemia of infancyV Chigot, P De Lonlay, M C Nassogne, et al.
AJNR. American Journal of Neuroradiology|May 30, 2015
Choroid Plexus Neoplasms: Toward a Distinction between Carcinoma and Papilloma Using Arterial Spin-LabelingV Dangouloff-Ros, D Grevent, M Pagès, et al.
Journal of Medical Genetics|May 6, 2014
Brain imaging in mitochondrial respiratory chain deficiency: combination of brain MRI features as a useful tool for genotype/phenotype correlationsM Bricout, D Grévent, A S Lebre, et al.
Pediatric Radiology|December 2, 2000
Intracranial venous anomalies associated with atretic cephalocoelesF Brunelle, J Baraton, D Renier, et al.
Clinical Genetics|September 29, 2009
Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression burstsF Molinari, A Kaminska, G Fiermonte, et al.
Hormone Research|July 15, 2000
Loss of imprinted genes and paternal SUR1 mutations lead to focal form of congenital hyperinsulinismJ C Fournet, C Mayaud, P de Lonlay, et al.
Revue Neurologique|April 29, 2014
[Aspect of brain MRI in mitochondrial respiratory chain deficiency. A diagnostic algorithm of the most common mitochondrial genetic mutations]M Devaux-Bricout, D Grévent, A-S Lebre, et al.
Pageof 25