Search Results - "Currier, R D"

Cutting the Gordian Knot: Standardizing Uncrewed Systems Data Formats by RD, Currier

“…The past several years has seen an explosion in the number of commercially available uncrewed systems. These systems range in size and complexity from the…”
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International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome by TROUILLAS, P, TAKAYANAGI, T, COUTINHO, P, HAMIDA, M. B, CAMPANELLA, G, FILLA, A, SCHUT, L, TIMANN, D, HONNORAT, J, NIGHOGHOSSIAN, N, MANYAM, B, HALLETT, M, CURRIER, R. D, SUBRAMONY, S. H, WESSEL, K, BRYER, A, DIENER, H. C, MASSAQUOI, S, GOMEZ, C. M

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The Big Four: Functional Assessment Research Informs Preventative Behavior Analysis by Ala’i-Rosales, Shahla, Cihon, Joseph H., Currier, Thomas D. R., Ferguson, Julia L., Leaf, Justin B., Leaf, Ron, McEachin, John, Weinkauf, Sara M.

“…Current practice guidelines suggest that the assessment and treatment of challenging behavior should consist of conducting a functional behavior assessment…”
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Familial patterns of prostate cancer: a case-control analysis by Spitz, M R, Currier, R D, Fueger, J J, Babaian, R J, Newell, G R

“…Epidemiological data have not yet enabled physicians to look beyond age and race to identify men at increased risk for prostate cancer. We conducted a…”
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Dominantly inherited cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia-I, Machado-Joseph disease, or Dentato-Rubro-Pallido-Luysian atrophy locus by Subramony, S H, Fratkin, J D, Manyam, B V, Currier, R D

“…The dominantly inherited ataxias are characterized both by phenotypic variability (phenotypic heterogeneity) within the same genotype and overlapping…”
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A medullary syndrome characterized by wild arm ataxia by CURRIER, R. D, BEBIN, J

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Familial progressive subcortical gliosis by LANSKA, D. J, CURRIER, R. D, COHEN, M, GAMBETTI, P, SMITH, E. E, BEBIN, J, JACKSON, J. F, WHITEHOUSE, P. J, MARKESBERY, W. R

“…We report clinical and pathologic findings from two kindreds afflicted with a familial form of progressive subcortical gliosis. The disorder segregated as an…”
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Intrafamilial variability in Machado-Joseph disease by Subramony, S H, Currier, R D

“…Dominantly inherited ataxias resulting from different gene mutations are difficult to distinguish based on clinical phenotypes. We believe the phenotypic…”
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Decreased parvalbumin immunoreactivity in surviving Purkinje cells of patients with spinocerebellar ataxia-1 by VIG, P. J. S, FRATKIN, J. D, DESAIAH, D, CURRIER, R. D, SUBRAMONY, S. H

“…The distribution of two calcium-binding proteins, calbindin D28k (CaBP) and parvalbumin (PV), was investigated by immunohistochemistry in the brains of three…”
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Hereditary adult-onset Alexander's disease with palatal myoclonus, spastic paraparesis, and cerebellar ataxia by Schwankhaus, J.D, Parisi, J.E, Gulledge, W.R, Chin, L, Currier, R.D

“…We describe a progressive neurologic disorder in three sisters characterized clinically by palatal myoclonus, spastic weakness, hyperreflexia, mild cerebellar…”
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Familial progressive subcortical gliosis : presence of prions and linkage to chromosome 17 by PETERSEN, R. B, TABATON, M, AUTILIO-GAMBETTI, L, WILHELMSEN, K. C, GAMBETTI, P, CHEN, S. G, MONARI, L, RICHARDSON, S. L, LYNCHES, T, MANETTO, V, LANSKA, D. J, MARKESBERY, W. R, CURRIER, R. D

“…Progressive subcortical gliosis (PSG) is a sporadic and familial dementing disease characterized pathologically by astrogliosis at the cortex-white matter…”
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Low dose oral methotrexate treatment of multiple sclerosis: a pilot study by Currier, R D, Haerer, A F, Meydrech, E F

“…An 18-month double-blind treatment of multiple sclerosis with low dose oral methotrexate showed it to be well tolerated and suggested effectiveness in…”
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Decreased insulin-like growth factor I-mediated protein tyrosine phosphorylation in human olivopontocerebellar atrophy and lurcher mutant mouse by Vig, P J, Desaiah, D, Joshi, P, Subramony, S H, Fratkin, J D, Currier, R D

“…We examined insulin-like growth factor I (IGF-I)-dependent phosphorylation and protein tyrosine kinase (PTK) activity in cerebellar cortex of normal humans,…”
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Orthostatic tremor in familial-essential tremor by WEE, A. S, SUBRAMONY, S. H, CURRIER, R. D

“…We studied a family with essential tremor of the arms. Some members also had tremor of the trunk and legs on standing, but not on walking, sitting, or…”
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Genotypes and phenotypes by Currier, R D, Subramony, S H

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Inositol 1,4,5-trisphosphate metabolism in the cerebella of Lurcher mutant mice and patients with olivopontocerebellar atrophy by Vig, P J, Subramony, S H, Currier, R D, Desaiah, D

“…We have investigated inositol 1,4,5-trisphosphate (InsP3) metabolism in cerebellar membranes of normal humans and patients with dominant ataxia ('C' kindred),…”
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Bilateral Ptosis due to Mesencephalic Lesions with Relative Preservation of Ocular Motility by Martin, Timothy J, Corbett, James J, Babikian, Paul V, Crawford, Stephen C, Currier, Robert D

“…Three cases of bilateral ptosis with relatively normal ocular motility are presented. In two of the patients, neuroimaging demonstrated lesions in the region…”
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Inositol 1,4,5-trisphosphate receptors and protein kinase C in olivopontocerebellar atrophy by Desaiah, D, Vig, P J, Subramony, S H, Currier, R D

“…We examined protein kinase C (PKC) activity and inositol 1,4,5-trisphosphate (InsP3) binding in frontal cortex (FC) and cerebellar cortex (CC) of normal…”
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A medullary syndrome characterized by wild arm ataxia by Jaster, J H, Smith, T W, Gleckman, A M, Currier, R D, Bebin, J

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Did John Hunter give James Parkinson an idea? by Currier, R D

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