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T de Barsy

Showing results (21-30 of 58) with videos related to

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Neurology|December 1, 1983
Idiopathic recurrent myoglobinuria and persistent weaknessC Bermils, S Tassin, J M Brucher, et al.
Revue Neurologique|January 1, 1990
[Intolerance to exercise caused by carnitine palmitoyltransferase deficiency]C Desnuelle, J F Pellissier, T de Barsy, et al.
Muscle & Nerve|March 1, 1979
Type III glycogenosis with multicore structuresJ F Pellissier, T de Barsy, M C Faugere, et al.
Clinical EEG (Electroencephalography)|April 1, 1990
Event-related potentials and cognitive functions in epileptic treated patientsK van Rijckevorsel-Harmant, D Flahaut, J Harman, et al.
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|October 1, 1974
Proceedings: Glycogen phosphorylase and its converter enzymes in cultured human fibroblastsB Lederer, T de Barsy, J G Leroy, et al.
Lancet (London, England)|August 11, 1990
Fluvoxamine: an antidepressant with low (or no) epileptogenic effectJ Harmant, K van Rijckevorsel-Harmant, T de Barsy, et al.
European Neurology|January 1, 1991
Bilateral tonic pupils and polyneuropathy in Sjögren's syndrome: a common pathophysiological mechanism?M P Waterschoot, J M Guerit, M Lambert, et al.
Journal of Computer Assisted Tomography|September 1, 1988
Brain metabolism in mitochondrial encephalomyopathy: a PET studyA De Volder, S Ghilain, T de Barsy, et al.
Birth Defects Original Article Series|March 1, 1973
Enzyme replacement in Pompe disease: an attempt with purified human acid alpha-glucosidaseT de Barsy, P Jacquemin, F Van Hoof, et al.
Acta Neuropathologica|February 19, 1973
Pompe's disease: an inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscleJ J Martin, T de Barsy, F van Hoof, et al.
Pageof 6

Showing results (21-30 of 58) with videos related to

Sort By:
Pageof 6
Neurology|December 1, 1983
Idiopathic recurrent myoglobinuria and persistent weaknessC Bermils, S Tassin, J M Brucher, et al.
Revue Neurologique|January 1, 1990
[Intolerance to exercise caused by carnitine palmitoyltransferase deficiency]C Desnuelle, J F Pellissier, T de Barsy, et al.
Muscle & Nerve|March 1, 1979
Type III glycogenosis with multicore structuresJ F Pellissier, T de Barsy, M C Faugere, et al.
Clinical EEG (Electroencephalography)|April 1, 1990
Event-related potentials and cognitive functions in epileptic treated patientsK van Rijckevorsel-Harmant, D Flahaut, J Harman, et al.
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|October 1, 1974
Proceedings: Glycogen phosphorylase and its converter enzymes in cultured human fibroblastsB Lederer, T de Barsy, J G Leroy, et al.
Lancet (London, England)|August 11, 1990
Fluvoxamine: an antidepressant with low (or no) epileptogenic effectJ Harmant, K van Rijckevorsel-Harmant, T de Barsy, et al.
European Neurology|January 1, 1991
Bilateral tonic pupils and polyneuropathy in Sjögren's syndrome: a common pathophysiological mechanism?M P Waterschoot, J M Guerit, M Lambert, et al.
Journal of Computer Assisted Tomography|September 1, 1988
Brain metabolism in mitochondrial encephalomyopathy: a PET studyA De Volder, S Ghilain, T de Barsy, et al.
Birth Defects Original Article Series|March 1, 1973
Enzyme replacement in Pompe disease: an attempt with purified human acid alpha-glucosidaseT de Barsy, P Jacquemin, F Van Hoof, et al.
Acta Neuropathologica|February 19, 1973
Pompe's disease: an inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscleJ J Martin, T de Barsy, F van Hoof, et al.
Pageof 6