Search Results - "Hudson, Arthur J."

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    Consciousness: physiological dependence on rapid memory access by Hudson, Arthur J

    Published in Frontiers in bioscience (01-01-2009)
    “…Consciousness develops from birth during the early months as the senses and other nervous system functions mature sufficiently to receive, process and store…”
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    Changes in sizes of cortical and lower motor neurons in amyotrophic lateral sclerosis by Kiernan, J A, Hudson, A J

    Published in Brain (London, England : 1878) (01-04-1991)
    “…It has been suggested that the degeneration of lower motor neurons in amyotrophic lateral sclerosis (ALS) is a transneuronal event, secondary to the loss of…”
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    Consciousness and cell memory: a dynamic epigenetic interrelationship by Hudson, Arthur J

    Published in Canadian journal of neurological sciences (01-09-2011)
    “…There have been great advances in the neurological sciences in recent years including some in the higher functions of the brain such as memory but one of the…”
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    Misidentification syndromes related to face specific area in the fusiform gyrus by Hudson, Arthur J, Grace, Gloria M

    “…The “delusional misidentification syndromes” are a group of uncommon and varied disorders in which, in typical form, the patient thinks that a particular…”
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    Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita) by George, Alfred L, Crackower, Michael A, Abdalla, Judith A, Hudson, Arthur J, Ebers, George C

    Published in Nature genetics (01-04-1993)
    “…Thomsen's disease (autosomal dominant myotonia congenita) has recently been linked to chromosome 7q35 in the region of the human skeletal muscle chloride…”
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    Pain perception and response: central nervous system mechanisms by Hudson, A J

    Published in Canadian journal of neurological sciences (01-02-2000)
    “…Although several decades of studies have detailed peripheral and ascending nociceptive pathways to the thalamus and cerebral cortex, pain is a symptom that has…”
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    Amyotrophic lateral sclerosis/parkinsonism/dementia: clinico-pathological correlations relevant to Guamanian ALS/PD by Hudson, A J

    Published in Canadian journal of neurological sciences (01-08-1991)
    “…In a recent report on the clinical and pathological features of Guamanian ALS/PD and post-encephalitic parkinsonism/ALS a number of similarities were…”
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    Anti-neurone antibodies are not characteristic of amyotrophic lateral sclerosis by Kiernan, J A, Hudson, A J

    Published in Neuroreport (01-04-1993)
    “…Autoantibodies, a suggested cause of motor neurone degeneration in amyotrophic lateral sclerosis (ALS), were sought immunohistochemically after applying…”
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    The incidence of amyotrophic lateral sclerosis in southwestern Ontario, Canada by HUDSON, A. J, DAVENPORT, A, HADER, W. J

    Published in Neurology (01-11-1986)
    “…The incidence, prevalence, and mortality rates of amyotrophic lateral sclerosis in southwestern Ontario, Canada, were determined for the years 1978 through…”
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    Insulin binding to myotonic dystrophy fibroblasts by Lam, L, Hudson, A J, Strickland, K P, Tevaarwerk, G J

    Published in Journal of the neurological sciences (01-02-1983)
    “…Insulin receptor binding was examined in cultured skin fibroblasts from 10 myotonic dystrophy patients and 10 age- and sex-matched control subjects. The…”
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    Chronic whiplash by Hudson, A J

    Published in Neurology (01-08-1996)
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    A familial syndrome of congenital cataract, mental impairment, and dentate gyrus atrophy by Hudson, A J, Munoz, D G

    Published in Annals of neurology (01-04-1997)
    “…We present a family with congenital cataract with, in some cases, mental retardation and emotional instability, but intellectual deterioration in all affected…”
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    Changes in shapes of surviving motor neurons in amyotrophic lateral sclerosis by Kiernan, J A, Hudson, A J

    Published in Brain (London, England : 1878) (01-02-1993)
    “…In amyotrophic lateral sclerosis, motor neurons in the spinal cord and brainstem shrink before they die. In 12 cases of sporadic amyotrophic lateral sclerosis,…”
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    Clinicopathological features of primary lateral sclerosis are different from amyotrophic lateral sclerosis by Hudson, A J, Kiernan, J A, Munoz, D G, Pringle, C E, Brown, W F, Ebers, G C

    Published in Brain research bulletin (1993)
    “…Primary lateral sclerosis (PLS) bears close resemblance to cases of amyotrophic lateral sclerosis (ALS) presenting with spasticity, but histopathological…”
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