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Journal of Inherited Metabolic Disease
|
January 1, 1982
Infantile phytanic acid storage disease, a possible variant of Refsum's disease: three cases, including ultrastructural studies of the liver
J M Scotto, M Hadchouel, M Odievre, et al.
European Journal of Clinical Pharmacology
|
January 1, 1996
Effect of stiripentol on carbamazepine plasma concentration and metabolism in epileptic children
A Tran, F Vauzelle-Kervroedan, E Rey, et al.
British Journal of Clinical Pharmacology
|
August 1, 1990
Pharmacokinetics of the individual enantiomers of vigabatrin (gamma-vinyl GABA) in epileptic children
E Rey, G Pons, M O Richard, et al.
Revue Neurologique
|
September 3, 1999
[Ictal SPECT in the epileptic child. Contribution of subtraction interictal images and superposition of with MRI]
C Chiron, P Véra, A Kaminska, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
May 1, 1992
Changes in regional cerebral blood flow during brain maturation in children and adolescents
C Chiron, C Raynaud, B Mazière, et al.
Neuropediatrics
|
November 19, 2010
Heterotopia associated with hippocampal sclerosis: an under-recognized cause of early onset epilepsy in children operated on for temporal lobe epilepsy
E López H, M Fohlen, A Lelouch-Tubiana, et al.
British Journal of Clinical Pharmacology
|
April 1, 1996
Influence of concurrent antiepileptic medication on the pharmacokinetics of lamotrigine as add-on therapy in epileptic children
F Vauzelle-Kervroëdan, E Rey, C Cieuta, et al.
Revue Neurologique
|
January 1, 1989
[Myasthenia and pregnancy: a clinical and immunologic study of 42 cases (21 neonatal myasthenia cases)]
B Eymard, E Morel, O Dulac, et al.
Human Genetics
|
April 1, 1992
Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20
A Malafosse, M Leboyer, O Dulac, et al.
Journal of Medical Genetics
|
October 1, 1992
De novo t(X;21)(q28;q11) in a girl with phenotypic features of Williams-Beuren syndrome
L Telvi, J M Pinard, R Ion, et al.
Page
of 24
Search research articles
Search
Showing results (191-200 of 233) with videos related to
Sort By:
Page
of 24
Journal of Inherited Metabolic Disease
|
January 1, 1982
Infantile phytanic acid storage disease, a possible variant of Refsum's disease: three cases, including ultrastructural studies of the liver
J M Scotto, M Hadchouel, M Odievre, et al.
European Journal of Clinical Pharmacology
|
January 1, 1996
Effect of stiripentol on carbamazepine plasma concentration and metabolism in epileptic children
A Tran, F Vauzelle-Kervroedan, E Rey, et al.
British Journal of Clinical Pharmacology
|
August 1, 1990
Pharmacokinetics of the individual enantiomers of vigabatrin (gamma-vinyl GABA) in epileptic children
E Rey, G Pons, M O Richard, et al.
Revue Neurologique
|
September 3, 1999
[Ictal SPECT in the epileptic child. Contribution of subtraction interictal images and superposition of with MRI]
C Chiron, P Véra, A Kaminska, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
May 1, 1992
Changes in regional cerebral blood flow during brain maturation in children and adolescents
C Chiron, C Raynaud, B Mazière, et al.
Neuropediatrics
|
November 19, 2010
Heterotopia associated with hippocampal sclerosis: an under-recognized cause of early onset epilepsy in children operated on for temporal lobe epilepsy
E López H, M Fohlen, A Lelouch-Tubiana, et al.
British Journal of Clinical Pharmacology
|
April 1, 1996
Influence of concurrent antiepileptic medication on the pharmacokinetics of lamotrigine as add-on therapy in epileptic children
F Vauzelle-Kervroëdan, E Rey, C Cieuta, et al.
Revue Neurologique
|
January 1, 1989
[Myasthenia and pregnancy: a clinical and immunologic study of 42 cases (21 neonatal myasthenia cases)]
B Eymard, E Morel, O Dulac, et al.
Human Genetics
|
April 1, 1992
Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20
A Malafosse, M Leboyer, O Dulac, et al.
Journal of Medical Genetics
|
October 1, 1992
De novo t(X;21)(q28;q11) in a girl with phenotypic features of Williams-Beuren syndrome
L Telvi, J M Pinard, R Ion, et al.
Page
of 24