Search Results - "Nakamuro, T."
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1
Drop in relapse rate of MS by combination therapy of three different phosphodiesterase inhibitors
Published in Multiple sclerosis (2000)“…Phosphodiesterase inhibitors (PDEIs), when used in combination, synergistically suppress TNFalpha production by various cells and also suppress experimental…”
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2
Hybrid survival motor neuron genes in Japanese patients with spinal muscular atrophy
Published in Acta neurologica Scandinavica (01-06-1999)“…Spinal muscular atrophy (SMA) is a frequently occurring autosomal recessive disease, characterized by the degeneration of spinal cord anterior horn cells,…”
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3
A patient of Charcot-Marie-tooth disease with rigid spine and respiratory failure
Published in Rinshō shinkeigaku (01-05-2000)“…This report describes a case of a 17-year-old girl with Charcot-Marie-Tooth disease (CMT) representing rigid spine and respiratory failure. At age 11, she…”
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4
Recurrent polyradiculoneuropathy with hyperthyroidism
Published in European neurology (1993)“…A 30-year-old woman, who had had two episodes of distal dominant sensorimotor disorders in the extremities, developed again sensorimotor involvement in the…”
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5
A clinicophysiologic study of central and peripheral motor conduction in hereditary demyelinating motor and sensory neuropathy
Published in Electromyography and clinical neurophysiology (01-03-1993)“…Central and peripheral motor nerve conduction were analyzed in 13 patients with hereditary demyelinating motor and sensory neuropathy using central magnetic…”
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6
Randomized, double-blind study of pramipexole with placebo and bromocriptine in advanced Parkinson's disease
Published in Movement disorders (01-10-2003)“…We compared the efficacy and safety of pramipexole (PPX) with placebo in the treatment of advanced Parkinson's disease (PD) as an adjunct to levodopa. A…”
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7
Central motor conduction time (CMCT) in hereditary motor sensory neuropathy type I (HMSN type I)
Published in Rinshō shinkeigaku (01-05-1990)“…The motor system of 13 cases with hereditary motor sensory neuropathy (HMSN) type I were analysed by clinical neurophysiological method. The motor conduction…”
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8
An MRI study of hereditary spinocerebellar degenerations
Published in Rinshō shinkeigaku (01-06-1990)“…We evaluated magnetic resonance image (MRI) in 21 cases of hereditary spinocerebellar degenerations (SCD) of autosomal dominant trait. By the discriminant…”
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9
Screaming during sleep in patients with Parkinson disease
Published in Rinshō shinkeigaku (01-05-1998)“…We studied 12 patients with Parkinson disease who scream while sleeping. All 12 patients showed clinical manifestations and brain images of typical idiopathic…”
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10
A case of Japanese encephalitis demonstrating characteristic changes in MRI
Published in Rinshō shinkeigaku (01-08-1991)“…A 40-year-old woman developed high fever and headache. Five days later, she was admitted because of consciousness disturbance and tremulous movements in upper…”
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11
A report of two siblings with both maternal dentato-rubro-pallido-luysian atrophy and paternal Ehlers-Danlos syndrome type III
Published in Rinshō shinkeigaku (01-03-1998)“…The report deals with the first description of two siblings, a 43-year-old woman and 39-year-old man, who have developed cerebellar ataxia, choreoathetosis,…”
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12
A case report of the compression syndrome due to hypertrophic neuropathy
Published in Rinshō shinkeigaku (01-02-1991)“…We reported a case of hypertrophic neuropathy of adult onset. The pathological change in the sural nerve was decreased axonal population with onion-bulb…”
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13
The kinesiological, chemical and pathological analysis in pulsed magnetic stimulation to the brain
Published in Rinshō shinkeigaku (01-08-1989)“…Pulsed magnetic stimulation of the human brain and spinal region has been reported recently. Unlike electrical stimulation, magnetic stimulation excites the…”
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14
A family with dentato-rubro-pallido-luysian atrophy (DRPLA): an intergenerational contraction of the CAG repeat
Published in Rinshō shinkeigaku (01-02-1997)“…We describe the relation of the CAG repeat length to the genetic anticipation in a Japanese family with dentato-rubro-pallido-luysian atrophy (DRPLA). The…”
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15
A case of juvenile-type distal and segmental muscular atrophy of upper extremities (Hirayama disease) with the isolated cervical fusion at the C3-C4 levels
Published in Rinshō shinkeigaku (01-05-1989)“…The case, 29-year-old male, had suffered from muscular weakness and atrophy of the bilateral forearms and hands with tremor of the bilateral fingers for about…”
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16
Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15q13-15
Published in Annals of neurology (01-07-2000)“…To date, three loci for autosomal recessive hereditary spastic paraplegia (ARHSP) linked to chromosomes 8p12‐q13, 16qter, and 15q13–15 have been characterized…”
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17
Electrophysiological studies in siblings of De Sanctis-Cacchione syndrome
Published in Rinshō shinkeigaku (01-04-1989)“…Multi-modality evoked potentials in two cases, who were siblings, of De Sanctis-Cacchione syndrome were reported. The case 1, who was elder sister of the case…”
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18
MRI study of hemiballism
Published in Rinshō shinkeigaku (01-01-1990)“…MRI findings of four hemiballism cases are described, and pathophysiology, pathogenesis and treatment of hemiballism are discussed. All cases had no family…”
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19
Central motor reorganization after anastomosis of the musculocutaneous and intercostal nerves following cervical root avulsion
Published in Annals of neurology (01-07-1995)“…In 4 patients with a complete upper limb palsy due to traumatic cervical root avulsion, surgical anastomosis of intercostal to musculocutaneous nerves was…”
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20
α-1-Antichymotrypsin gene polymorphism and susceptibility to multiple system atrophy (MSA)
Published in Brain research. Molecular brain research. (18-08-2005)“…We investigated three genotypes (AA, AT, and TT) produced by signal peptide polymorphism of the α-1-antichymotrypsin (ACT) gene in 105 patients with multiple…”
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