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J Julien

Showing results (211-220 of 222) with videos related to

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Science (New York, N.Y.)|October 30, 1992
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphismL G Goldfarb, R B Petersen, M Tabaton, et al.
AJR. American Journal of Roentgenology|December 1, 1986
MR imaging of pulmonary emboli: an experimental study in dogsM G Stein, J V Crues, W G Bradley, et al.
Brain Pathology (Zurich, Switzerland)|July 21, 1998
Clinical features of fatal familial insomnia: phenotypic variability in relation to a polymorphism at codon 129 of the prion protein geneP Montagna, P Cortelli, P Avoni, et al.
JTO Clinical and Research Reports|February 27, 2023
Safety and Efficacy Outcomes From a Single-Center Study of Image-Guided Percutaneous Microwave Ablation for Primary and Metastatic Lung MalignancyStephen M Chan, Peter J Julien, Peter Kaganjo, et al.
Annals of Neurology|April 1, 1996
Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological featuresA Dürr, G Stevanin, G Cancel, et al.
Nature Medicine|September 1, 1997
Allelic origin of the abnormal prion protein isoform in familial prion diseasesS G Chen, P Parchi, P Brown, et al.
Acta Neuropathologica|July 27, 2000
Chronic inflammatory demyelinating polyneuropathy associated with dysglobulinemia: a peripheral nerve biopsy study in 18 casesA Vital, A Lagueny, J Julien, et al.
Ultrastructural Pathology|February 24, 2001
Chronic inflammatory demyelinating polyneuropathy: immunopathological and ultrastructural study of peripheral nerve biopsy in 42 casesC Vital, A Vital, A Lagueny, et al.
Annals of Neurology|August 12, 1999
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjectsP Parchi, A Giese, S Capellari, et al.
American Journal of Human Genetics|January 23, 1999
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxiaA Ducros, C Denier, A Joutel, et al.
Pageof 23

Showing results (211-220 of 222) with videos related to

Sort By:
Pageof 23
Science (New York, N.Y.)|October 30, 1992
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphismL G Goldfarb, R B Petersen, M Tabaton, et al.
AJR. American Journal of Roentgenology|December 1, 1986
MR imaging of pulmonary emboli: an experimental study in dogsM G Stein, J V Crues, W G Bradley, et al.
Brain Pathology (Zurich, Switzerland)|July 21, 1998
Clinical features of fatal familial insomnia: phenotypic variability in relation to a polymorphism at codon 129 of the prion protein geneP Montagna, P Cortelli, P Avoni, et al.
JTO Clinical and Research Reports|February 27, 2023
Safety and Efficacy Outcomes From a Single-Center Study of Image-Guided Percutaneous Microwave Ablation for Primary and Metastatic Lung MalignancyStephen M Chan, Peter J Julien, Peter Kaganjo, et al.
Annals of Neurology|April 1, 1996
Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological featuresA Dürr, G Stevanin, G Cancel, et al.
Nature Medicine|September 1, 1997
Allelic origin of the abnormal prion protein isoform in familial prion diseasesS G Chen, P Parchi, P Brown, et al.
Acta Neuropathologica|July 27, 2000
Chronic inflammatory demyelinating polyneuropathy associated with dysglobulinemia: a peripheral nerve biopsy study in 18 casesA Vital, A Lagueny, J Julien, et al.
Ultrastructural Pathology|February 24, 2001
Chronic inflammatory demyelinating polyneuropathy: immunopathological and ultrastructural study of peripheral nerve biopsy in 42 casesC Vital, A Vital, A Lagueny, et al.
Annals of Neurology|August 12, 1999
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjectsP Parchi, A Giese, S Capellari, et al.
American Journal of Human Genetics|January 23, 1999
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxiaA Ducros, C Denier, A Joutel, et al.
Pageof 23