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I J Butler

Showing results (61-70 of 89) with videos related to

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The Journal of Pediatrics|March 1, 1976
Diencephalic syndrome revisitedI M Burr, A E Slonim, R K Danish, et al.
Annals of Neurology|July 1, 1979
Biogenic amine metabolism in Tourette syndromeI J Butler, S H Koslow, W E Seifert, et al.
Annals of Neurology|October 1, 1982
Dopaminergic dsyfunction in Tourette syndromeH S Singer, I J Butler, L E Tune, et al.
Journal of Child Neurology|July 1, 1993
Proton magnetic resonance imaging and spectroscopic studies of the pathogenesis and treatment of juvenile dermatomyositisJ M Slopis, E F Jackson, P A Narayana, et al.
The New England Journal of Medicine|October 10, 1985
Reduction of biogenic amine levels in the Rett syndromeH Y Zoghbi, A K Percy, D G Glaze, et al.
Neurology|August 1, 1984
Short-latency somatosensory evoked potentials in the management of patients with achondroplasiaF W Nelson, W D Goldie, J T Hecht, et al.
Transactions of the American Neurological Association|January 1, 1975
Dihydropteridine reductase deficiency variant of phenylketonuria: a disorder of neurotransmittersI J Butler, A Krumholz, N A Holtzman, et al.
Archives of Neurology|May 18, 2001
Neurologic and psychiatric manifestations in a family with a mutation in exon 2 of the guanosine triphosphate-cyclohydrolase geneH Hahn, M R Trant, M J Brownstein, et al.
The Journal of Pediatrics|November 1, 1976
Hyperphenylalaninemia due to dihydropteridine reductase deficiency. Assay of the enzyme in fibroblasts from affected infants, heterozygotes, and in normal amniotic fluid cellsS Milstien, N A Holtzman, M E O'Flynn, et al.
The New England Journal of Medicine|July 19, 1984
Progressive neurologic deterioration and renal failure due to storage of glutamyl ribose-5-phosphateJ C Williams, I J Butler, H S Rosenberg, et al.
Pageof 9

Showing results (61-70 of 89) with videos related to

Sort By:
Pageof 9
The Journal of Pediatrics|March 1, 1976
Diencephalic syndrome revisitedI M Burr, A E Slonim, R K Danish, et al.
Annals of Neurology|July 1, 1979
Biogenic amine metabolism in Tourette syndromeI J Butler, S H Koslow, W E Seifert, et al.
Annals of Neurology|October 1, 1982
Dopaminergic dsyfunction in Tourette syndromeH S Singer, I J Butler, L E Tune, et al.
Journal of Child Neurology|July 1, 1993
Proton magnetic resonance imaging and spectroscopic studies of the pathogenesis and treatment of juvenile dermatomyositisJ M Slopis, E F Jackson, P A Narayana, et al.
The New England Journal of Medicine|October 10, 1985
Reduction of biogenic amine levels in the Rett syndromeH Y Zoghbi, A K Percy, D G Glaze, et al.
Neurology|August 1, 1984
Short-latency somatosensory evoked potentials in the management of patients with achondroplasiaF W Nelson, W D Goldie, J T Hecht, et al.
Transactions of the American Neurological Association|January 1, 1975
Dihydropteridine reductase deficiency variant of phenylketonuria: a disorder of neurotransmittersI J Butler, A Krumholz, N A Holtzman, et al.
Archives of Neurology|May 18, 2001
Neurologic and psychiatric manifestations in a family with a mutation in exon 2 of the guanosine triphosphate-cyclohydrolase geneH Hahn, M R Trant, M J Brownstein, et al.
The Journal of Pediatrics|November 1, 1976
Hyperphenylalaninemia due to dihydropteridine reductase deficiency. Assay of the enzyme in fibroblasts from affected infants, heterozygotes, and in normal amniotic fluid cellsS Milstien, N A Holtzman, M E O'Flynn, et al.
The New England Journal of Medicine|July 19, 1984
Progressive neurologic deterioration and renal failure due to storage of glutamyl ribose-5-phosphateJ C Williams, I J Butler, H S Rosenberg, et al.
Pageof 9