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Showing results (61-70 of 96) with videos related to

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Neurology|April 1, 1992
Major and minor birth malformations and antiepileptic drugsS Koch, G Lösche, E Jager-Romän, et al.
The Journal of Clinical Investigation|April 20, 1999
Large neutral amino acids block phenylalanine transport into brain tissue in patients with phenylketonuriaJ Pietz, R Kreis, A Rupp, et al.
Pediatric Pharmacology (New York, N.Y.)|January 1, 1983
Carbamazepine and carbamazepine-10,11- epoxide during pregnancy and postnatal period in epileptic mother and their nursed infants: pharmacokinetics and clinical effectsW Kuhnz, E Jäger-Roman, D Rating, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
4-Hydroxybutyric aciduria: a new inborn error of metabolism. III. Enzymology and inheritanceK M Gibson, I Jansen, L Sweetman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1983
Succinic semialdehyde dehydrogenase deficiency: an inborn error of gamma-aminobutyric acid metabolismK M Gibson, L Sweetman, W L Nyhan, et al.
European Journal of Pediatrics|November 11, 1998
Neurological outcome in adult patients with early-treated phenylketonuriaJ Pietz, R Dunckelmann, A Rupp, et al.
British Journal of Cancer|November 16, 2002
Treatment of paediatric pontine glioma with oral trophosphamide and etoposideJ E A Wolff, S Westphal, G Mölenkamp, et al.
European Journal of Pediatrics|January 1, 1994
Neurological manifestations of organic acid disordersG F Hoffmann, K M Gibson, F K Trefz, et al.
Neuropediatrics|November 9, 2000
Nonconvulsive status epilepticus--a possible cause of mental retardation in patients with Lennox-Gastaut syndromeM Hoffmann-Riem, W Diener, C Benninger, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Folinic acid responsive seizures: a new syndrome?K Hyland, N R Buist, B R Powell, et al.
Pageof 10

Showing results (61-70 of 96) with videos related to

Sort By:
Pageof 10
Neurology|April 1, 1992
Major and minor birth malformations and antiepileptic drugsS Koch, G Lösche, E Jager-Romän, et al.
The Journal of Clinical Investigation|April 20, 1999
Large neutral amino acids block phenylalanine transport into brain tissue in patients with phenylketonuriaJ Pietz, R Kreis, A Rupp, et al.
Pediatric Pharmacology (New York, N.Y.)|January 1, 1983
Carbamazepine and carbamazepine-10,11- epoxide during pregnancy and postnatal period in epileptic mother and their nursed infants: pharmacokinetics and clinical effectsW Kuhnz, E Jäger-Roman, D Rating, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
4-Hydroxybutyric aciduria: a new inborn error of metabolism. III. Enzymology and inheritanceK M Gibson, I Jansen, L Sweetman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1983
Succinic semialdehyde dehydrogenase deficiency: an inborn error of gamma-aminobutyric acid metabolismK M Gibson, L Sweetman, W L Nyhan, et al.
European Journal of Pediatrics|November 11, 1998
Neurological outcome in adult patients with early-treated phenylketonuriaJ Pietz, R Dunckelmann, A Rupp, et al.
British Journal of Cancer|November 16, 2002
Treatment of paediatric pontine glioma with oral trophosphamide and etoposideJ E A Wolff, S Westphal, G Mölenkamp, et al.
European Journal of Pediatrics|January 1, 1994
Neurological manifestations of organic acid disordersG F Hoffmann, K M Gibson, F K Trefz, et al.
Neuropediatrics|November 9, 2000
Nonconvulsive status epilepticus--a possible cause of mental retardation in patients with Lennox-Gastaut syndromeM Hoffmann-Riem, W Diener, C Benninger, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Folinic acid responsive seizures: a new syndrome?K Hyland, N R Buist, B R Powell, et al.
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