Search research articles
Contact Us
Filters
Showing results (21-30 of 58) with videos related to
Page
of 6
Sort By:
Neurology
|
December 1, 1983
Idiopathic recurrent myoglobinuria and persistent weakness
C 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 structures
J 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 patients
K 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 fibroblasts
B Lederer, T de Barsy, J G Leroy, et al.
Lancet (London, England)
|
August 11, 1990
Fluvoxamine: an antidepressant with low (or no) epileptogenic effect
J 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 study
A 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-glucosidase
T 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 muscle
J J Martin, T de Barsy, F van Hoof, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 58) with videos related to
Sort By:
Page
of 6
Neurology
|
December 1, 1983
Idiopathic recurrent myoglobinuria and persistent weakness
C 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 structures
J 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 patients
K 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 fibroblasts
B Lederer, T de Barsy, J G Leroy, et al.
Lancet (London, England)
|
August 11, 1990
Fluvoxamine: an antidepressant with low (or no) epileptogenic effect
J 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 study
A 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-glucosidase
T 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 muscle
J J Martin, T de Barsy, F van Hoof, et al.
Page
of 6