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

T de Barsy

Showing results (11-20 of 58) with videos related to

Pageof 6
Sort By:
Biochemical Society Transactions|January 1, 1975
The cellular distribution of lipososmes in the liver of newborn ratsT de Barsy, P Devos, F Van Hoof
Laboratory Investigation; a Journal of Technical Methods and Pathology|March 1, 1976
A morphologic and biochemical study of the fate of antibody-bearing liposomesT de Barsy, P Devos, F Van Hoof
Revue Neurologique|October 17, 1998
[Bradycardia: an unrecognized complication of some epileptic crises]F Saussu, K van Rijckevorsel, T de Barsy
Acta Neuropathologica|August 1, 1979
Uncommon case of type II glycogenosisT de Barsy, G Ferrière, E Fernandez-Alvarez
Seizure|September 1, 1995
Bradycardia, an epileptic ictal manifestationK van Rijckevorsel, F Saussu, T de Barsy
Klinische Padiatrie|September 1, 1981
[Liver fructose-1-phosphate and fructose-1,6-diphosphate aldolase deficiency in hereditary fructose intolerance (author's transl)]R Joosten, M Berzdorf, T de Barsy, et al.
Journal of Neurology|August 6, 1976
Acid maltase deficiency in non-identical adult twins. A morphological and biochemical studyJ J Martin, T de Barsy, W R den Tandt
European Journal of Biochemistry|November 21, 1972
Rodent and human acid -glucosidase. Purification, properties and inhibition by antibodies. Investigation in type II glycogenosisT de Barsy, P Jacquemin, P Devos, et al.
Archives Francaises De Pediatrie|December 1, 1981
[A study of the abnormal polysaccharide in a child with type IV glycogen storage disease (author's transl)]J M Scotto, T de Barsy, M Hadchouel, et al.
Clinical Neurology and Neurosurgery|January 1, 1985
Muscle carnitine deficiency in old age. Case report and therapeutic resultsJ J Martin, A Vercruyssen, T de Barsy, et al.
Pageof 6

Showing results (11-20 of 58) with videos related to

Sort By:
Pageof 6
Biochemical Society Transactions|January 1, 1975
The cellular distribution of lipososmes in the liver of newborn ratsT de Barsy, P Devos, F Van Hoof
Laboratory Investigation; a Journal of Technical Methods and Pathology|March 1, 1976
A morphologic and biochemical study of the fate of antibody-bearing liposomesT de Barsy, P Devos, F Van Hoof
Revue Neurologique|October 17, 1998
[Bradycardia: an unrecognized complication of some epileptic crises]F Saussu, K van Rijckevorsel, T de Barsy
Acta Neuropathologica|August 1, 1979
Uncommon case of type II glycogenosisT de Barsy, G Ferrière, E Fernandez-Alvarez
Seizure|September 1, 1995
Bradycardia, an epileptic ictal manifestationK van Rijckevorsel, F Saussu, T de Barsy
Klinische Padiatrie|September 1, 1981
[Liver fructose-1-phosphate and fructose-1,6-diphosphate aldolase deficiency in hereditary fructose intolerance (author's transl)]R Joosten, M Berzdorf, T de Barsy, et al.
Journal of Neurology|August 6, 1976
Acid maltase deficiency in non-identical adult twins. A morphological and biochemical studyJ J Martin, T de Barsy, W R den Tandt
European Journal of Biochemistry|November 21, 1972
Rodent and human acid -glucosidase. Purification, properties and inhibition by antibodies. Investigation in type II glycogenosisT de Barsy, P Jacquemin, P Devos, et al.
Archives Francaises De Pediatrie|December 1, 1981
[A study of the abnormal polysaccharide in a child with type IV glycogen storage disease (author's transl)]J M Scotto, T de Barsy, M Hadchouel, et al.
Clinical Neurology and Neurosurgery|January 1, 1985
Muscle carnitine deficiency in old age. Case report and therapeutic resultsJ J Martin, A Vercruyssen, T de Barsy, et al.
Pageof 6