Search Results - "Hutchison, H T"

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    Subacute sclerosing panencephalitis in the differential diagnosis of encephalitis by HONARMAND, S, GLASER, C. A, CHOW, E, SEJVAR, J. J, PREAS, C. P, COSENTINO, G. C, HUTCHISON, H. T, BELLINI, W. J

    Published in Neurology (26-10-2004)
    “…The authors describe five cases of subacute sclerosing panencephalitis (SSPE) identified through the California Encephalitis Project that emphasize the…”
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    High-affinity transport of glutamate in rat brain microvessels by Hutchison, H T, Eisenberg, H M, Haber, B

    Published in Experimental neurology (01-02-1985)
    “…The maintenance of low extracellular concentrations of glutamate in the brain is a complex process in which the role of capillary transport is poorly…”
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    134 MATERNAL AND CHILD THROMBOPHILIA IN NEONATAL STROKE by Curry, C. J., Bhullar, S., Holmes, J., Hutchison, H. T.

    Published in Journal of investigative medicine (01-01-2005)
    “…Several studies have implicated inherited and acquired thrombophilia as etiologically important in neonatal stroke (NS). In few have both mothers and children…”
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    Differential diagnosis and treatment of conversion disorder and Guillain-Barre syndrome by Wherry, J N, McMillan, S L, Hutchison, H T

    Published in Clinical pediatrics (01-10-1991)
    “…Three cases are presented which illustrate the possible difficulties in differentiating between the diagnoses of Guillain-Barre Syndrome and conversion…”
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    Temperature-sensitive Yeast Mutant Defective in Ribonucleic Acid Production by Hutchison, H T, Hartwell, L H, McLaughlin, C S

    Published in Journal of Bacteriology (01-09-1969)
    “…Article Usage Stats Services JB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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    Endothelial growth factor present in tissue culture of CNS tumors by Kelly, P J, Suddith, R L, Hutchison, H T, Werrbach, K, Haber, B

    Published in Journal of neurosurgery (01-03-1976)
    “…Human endothelial cells obtained from postpartum umbilical veins and placed in primary tissue cultures were treated with media from cultures of human and…”
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    Macromolecule Synthesis in Yeast Spheroplasts by Hutchison, H T, Hartwell, L H

    Published in Journal of Bacteriology (01-11-1967)
    “…Article Usage Stats Services JB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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    HLA antigen frequency in erythema multiforme and in recurrent herpes simplex by Middleton, D, Hutchison, T H, Lynd, J

    Published in Tissue antigens (01-03-1983)
    “…In this study the HLA antigen frequency was determined in a group of patients with erythema multiforme and in a separate group of patients with recurrent…”
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    In vitro Demonstration of an Endothelial Proliferative Factor Produced by Neural Cell Lines by Suddith, R. L., Kelly, P. J., Hutchison, H. T., Murray, E. A., Haber, B.

    “…Cultured endothelial cells exhibit a six- to tenfold increase in thymidine labeling index in response to a soluble factor elaborated by clonal cell lines of…”
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    Ocular, cerebral and cutaneous malformations: confirmation of an association by Ferguson, J W, Hutchison, H T, Rouse, B M

    Published in Clinical genetics (01-05-1984)
    “…A newborn with multiple congenital abnormalities including an orbital cyst, cerebral cysts, skin tags and focal dermal defects is described. This case is…”
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    Uptake of neurotransmitters and precursors by clonal lines of astrocytoma and neuroblastoma: III. Transport of choline by Hutchison, H T, Suddith, R L, Risk, M, Haber, B

    Published in Neurochemical research (01-04-1976)
    “…Clonal lines of glial, neuronal, and nonneural origin accumulate choline via a high-affinity carrier-mediated transport system withK m in the range of 10-14…”
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    Pyruvate carboxylase activity in subacute necrotizing encephalopathy (Leigh's disease) by SANDER, J, PACKMAN, S, BERG, B. O, HUTCHINSON, H. T, CASWELL, N

    Published in Neurology (01-04-1984)
    “…Leigh's disease is a heterogeneous group of disorders, in which clinical and biochemical features suggest abnormal pyruvate metabolism. In two patients with…”
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