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Drop in relapse rate of MS by combination therapy of three different phosphodiesterase inhibitors

Multiple sclerosis, 2000, Vol.6 (1), p.56-58

2000

Volltextzugriff (PDF)

A patient of Charcot-Marie-tooth disease with rigid spine and respiratory failure

Rinshō shinkeigaku, 2000-05, Vol.40 (5), p.433

2000

Volltextzugriff (PDF)

Hybrid survival motor neuron genes in Japanese patients with spinal muscular atrophy

Acta neurologica Scandinavica, 1999-06, Vol.99 (6), p.374-380

1999

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Randomized, double-blind study of pramipexole with placebo and bromocriptine in advanced Parkinson's disease

Movement disorders, 2003-10, Vol.18 (10), p.1149-1156

2003

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Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15q13-15

Annals of neurology, 2000-07, Vol.48 (1), p.108-112

2000

Volltextzugriff (PDF)

Recurrent polyradiculoneuropathy with hyperthyroidism

European neurology, 1993, Vol.33 (3), p.238

1993

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Central motor reorganization after anastomosis of the musculocutaneous and intercostal nerves following cervical root avulsion

Annals of neurology, 1995-07, Vol.38 (1), p.15-20

1995

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Central motor conduction time (CMCT) in hereditary motor sensory neuropathy type I (HMSN type I)

Rinshō shinkeigaku, 1990-05, Vol.30 (5), p.487

1990

Volltextzugriff (PDF)

α-1-Antichymotrypsin gene polymorphism and susceptibility to multiple system atrophy (MSA)

Brain research. Molecular brain research., 2005-08, Vol.138 (2), p.178-181

2005

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An MRI study of hereditary spinocerebellar degenerations

Rinshō shinkeigaku, 1990-06, Vol.30 (6), p.610

1990

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A case of Japanese encephalitis demonstrating characteristic changes in MRI

Rinshō shinkeigaku, 1991-08, Vol.31 (8), p.869

1991

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A clinicophysiologic study of central and peripheral motor conduction in hereditary demyelinating motor and sensory neuropathy

Electromyography and clinical neurophysiology, 1993-03, Vol.33 (2), p.101

1993

Volltextzugriff (PDF)

A case report of the compression syndrome due to hypertrophic neuropathy

Rinshō shinkeigaku, 1991-02, Vol.31 (2), p.213

1991

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The kinesiological, chemical and pathological analysis in pulsed magnetic stimulation to the brain

Rinshō shinkeigaku, 1989-08, Vol.29 (8), p.982

1989

Volltextzugriff (PDF)

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

Rinshō shinkeigaku, 1989-05, Vol.29 (5), p.639

1989

Volltextzugriff (PDF)

Electrophysiological studies in siblings of De Sanctis-Cacchione syndrome

Rinshō shinkeigaku, 1989-04, Vol.29 (4), p.497

1989

Volltextzugriff (PDF)

Drop in relapse rate of MS by combination therapy of three different phosphodiesterase inhibitors

Multiple sclerosis, 2000-02, Vol.6 (1), p.56-58

2000

Volltextzugriff (PDF)

Sweat function in Parkinson's disease

Journal of neurology, 1994-10, Vol.241 (10), p.573-576

1994

Volltextzugriff (PDF)

Screaming during sleep in patients with Parkinson disease

Rinshō shinkeigaku, 1998-05, Vol.38 (5), p.457

1998

Volltextzugriff (PDF)

A new model system for studying lacrimal physiology using cultured lacrimal gland acinar cells on Matrigel rafts

Advances in experimental medicine and biology, 2002, Vol.506 (Pt A), p.159

2002

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A report of two siblings with both maternal dentato-rubro-pallido-luysian atrophy and paternal Ehlers-Danlos syndrome type III

Rinshō shinkeigaku, 1998-03, Vol.38 (3), p.233

1998

Volltextzugriff (PDF)

A family with dentato-rubro-pallido-luysian atrophy (DRPLA): an intergenerational contraction of the CAG repeat

Rinshō shinkeigaku, 1997-02, Vol.37 (2), p.127

1997

Volltextzugriff (PDF)

Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15

Annals of neurology, 2000-07, Vol.48 (1), p.108-112

2000

Volltextzugriff (PDF)

Ceruletide therapy in action tremor following thalamic hemorrhage

Journal of neurology, 1993, Vol.240 (3), p.144-148

1993

Volltextzugriff (PDF)

MRI study of hemiballism

Rinshō shinkeigaku, 1990-01, Vol.30 (1), p.17

1990

Volltextzugriff (PDF)

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Drop in relapse rate of MS by combination therapy of three different phosphodiesterase inhibitors

A patient of Charcot-Marie-tooth disease with rigid spine and respiratory failure

Hybrid survival motor neuron genes in Japanese patients with spinal muscular atrophy

Randomized, double-blind study of pramipexole with placebo and bromocriptine in advanced Parkinson's disease

Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15q13-15

Recurrent polyradiculoneuropathy with hyperthyroidism

Central motor reorganization after anastomosis of the musculocutaneous and intercostal nerves following cervical root avulsion

Central motor conduction time (CMCT) in hereditary motor sensory neuropathy type I (HMSN type I)

α-1-Antichymotrypsin gene polymorphism and susceptibility to multiple system atrophy (MSA)

An MRI study of hereditary spinocerebellar degenerations

A case of Japanese encephalitis demonstrating characteristic changes in MRI

A clinicophysiologic study of central and peripheral motor conduction in hereditary demyelinating motor and sensory neuropathy

A case report of the compression syndrome due to hypertrophic neuropathy

The kinesiological, chemical and pathological analysis in pulsed magnetic stimulation to the brain

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

Electrophysiological studies in siblings of De Sanctis-Cacchione syndrome

Drop in relapse rate of MS by combination therapy of three different phosphodiesterase inhibitors

Sweat function in Parkinson's disease

Screaming during sleep in patients with Parkinson disease

A new model system for studying lacrimal physiology using cultured lacrimal gland acinar cells on Matrigel rafts

A report of two siblings with both maternal dentato-rubro-pallido-luysian atrophy and paternal Ehlers-Danlos syndrome type III

A family with dentato-rubro-pallido-luysian atrophy (DRPLA): an intergenerational contraction of the CAG repeat

Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15

Ceruletide therapy in action tremor following thalamic hemorrhage

MRI study of hemiballism

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