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J T Pelekanos

Showing results (1-10 of 6) with videos related to

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Pediatric Neurology|January 1, 1989
Melioidosis with multiple cerebral abscessesJ T Pelekanos, D B Appleton
Australian and New Zealand Journal of Ophthalmology|November 1, 1996
Coexistent orbital and cerebellar venous anomalies in linear sebaceous naevus syndromeA A Seawright, T J Sullivan, J T Pelekanos, et al.
Neurology|April 1, 1990
Stretch syncope in adolescenceJ T Pelekanos, J M Dooley, P R Camfield, et al.
Journal of Pediatric Gastroenterology and Nutrition|April 1, 1990
Protein turnover in malnourished patients with cystic fibrosis: effects of elemental and nonelemental nutritional supplementsJ T Pelekanos, T L Holt, L C Ward, et al.
Neurology|September 29, 2004
Failure to confirm association of a polymorphism in ABCB1 with multidrug-resistant epilepsyN C K Tan, S E Heron, I E Scheffer, et al.
Journal of Paediatrics and Child Health|May 23, 2006
Seizures, ataxia, developmental delay and the general paediatrician: glucose transporter 1 deficiency syndromeDavid J Coman, K G Sinclair, C J Burke, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Pediatric Neurology|January 1, 1989
Melioidosis with multiple cerebral abscessesJ T Pelekanos, D B Appleton
Australian and New Zealand Journal of Ophthalmology|November 1, 1996
Coexistent orbital and cerebellar venous anomalies in linear sebaceous naevus syndromeA A Seawright, T J Sullivan, J T Pelekanos, et al.
Neurology|April 1, 1990
Stretch syncope in adolescenceJ T Pelekanos, J M Dooley, P R Camfield, et al.
Journal of Pediatric Gastroenterology and Nutrition|April 1, 1990
Protein turnover in malnourished patients with cystic fibrosis: effects of elemental and nonelemental nutritional supplementsJ T Pelekanos, T L Holt, L C Ward, et al.
Neurology|September 29, 2004
Failure to confirm association of a polymorphism in ABCB1 with multidrug-resistant epilepsyN C K Tan, S E Heron, I E Scheffer, et al.
Journal of Paediatrics and Child Health|May 23, 2006
Seizures, ataxia, developmental delay and the general paediatrician: glucose transporter 1 deficiency syndromeDavid J Coman, K G Sinclair, C J Burke, et al.
Pageof 1