User profiles for I.J. Namer
 | IJ NAMERUniversité de Strasbourg, Institut de Cancérologie Strasbourg Europe, CHU de Strasbourg Verified email at unistra.fr Cited by 6094 |
Magnetic resonance imaging in the study of the lithium–pilocarpine model of temporal lobe epilepsy in adult rats
Purpose: In temporal lobe epilepsy, it remains to be clarified whether hippocampal sclerosis
is the cause or the consequence of epilepsy. We studied the temporal evolution of the …
is the cause or the consequence of epilepsy. We studied the temporal evolution of the …
Predictive value of cortical injury for the development of temporal lobe epilepsy in 21‐day‐old rats: an MRI approach using the lithium‐pilocarpine model
Purpose: Patients with temporal lobe epilepsy (TLE) usually had an initial precipitating
injury in early childhood. However, epilepsy does not develop in all children who have …
injury in early childhood. However, epilepsy does not develop in all children who have …
Enhanced-reality video fluorescence: a real-time assessment of intestinal viability
Objective: Our aim was to evaluate a fluorescence-based enhanced-reality system to assess
intestinal viability in a laparoscopic mesenteric ischemia model. Materials and Methods: A …
intestinal viability in a laparoscopic mesenteric ischemia model. Materials and Methods: A …
PET/CT-guided interventions: Indications, advantages, disadvantages and the state of the art
…, P Addeo, P Bachellier, IJ Namer… - … Invasive Therapy & …, 2018 - Taylor & Francis
Positron emission tomography/computed tomography (PET/CT) represents an emerging
imaging guidance modality that has been applied to successfully guide percutaneous …
imaging guidance modality that has been applied to successfully guide percutaneous …
Neuroimaging in Cockayne syndrome
…, F Sauvanaud, H Dollfus, IJ Namer… - American journal …, 2010 - Am Soc Neuroradiology
CS is an autosomal recessive multisystem disorder, which is mainly characterized by
neurologic and sensory impairment, cachectic dwarfism, and photosensitivity. We describe the …
neurologic and sensory impairment, cachectic dwarfism, and photosensitivity. We describe the …
Natural History and Phenotypic Spectrum of GAA‐FGF14 Sporadic Late‐Onset Cerebellar Ataxia (SCA27B)
Background Heterozygous GAA expansions in the FGF14 gene have been related to autosomal
dominant cerebellar ataxia (SCA27B‐MIM:620174). Whether they represent a common …
dominant cerebellar ataxia (SCA27B‐MIM:620174). Whether they represent a common …
SPG11 spastic paraplegia: a new cause of juvenile parkinsonism
Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC)
is a rare neurodegenerative disorder often caused by mutations in the gene encoding for …
is a rare neurodegenerative disorder often caused by mutations in the gene encoding for …
Pathogenesis and Pharmacology of Epilepsy in the Lithium‐pilocarpine Model
To try to identify the critical structures during epileptogenesis, we used the lithium‐pilocarpine
model that reproduces most clinical and neuropathological features of temporal lobe …
model that reproduces most clinical and neuropathological features of temporal lobe …
[HTML][HTML] Metabolome profiling by HRMAS NMR spectroscopy of pheochromocytomas and paragangliomas detects SDH deficiency: clinical and pathophysiological …
Succinate dehydrogenase gene (SDHx) mutations increase susceptibility to develop
pheochromocytomas/paragangliomas (PHEOs/PGLs). In the present study, we evaluate the …
pheochromocytomas/paragangliomas (PHEOs/PGLs). In the present study, we evaluate the …
18F-FDOPA PET/CT imaging of insulinoma revisited
…, F Moreau, P Bachellier, B Guillet, IJ Namer… - European journal of …, 2015 - Springer
Purpose 18 F-FDOPA PET imaging is increasingly used in the work-up of patients with
neuroendocrine tumours. It has been shown to be of limited value in localizing pancreatic insulin-…
neuroendocrine tumours. It has been shown to be of limited value in localizing pancreatic insulin-…