UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 383

Sortiert nach

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

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

2000

Link zum Volltext

Verfügbarkeit prüfen

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

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

1999

Link zum Volltext

Verfügbarkeit prüfen

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

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

2000

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

Recurrent polyradiculoneuropathy with hyperthyroidism

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

1993

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

An MRI study of hereditary spinocerebellar degenerations

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

1990

Link zum Volltext

Verfügbarkeit prüfen

A case of Japanese encephalitis demonstrating characteristic changes in MRI

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

1991

Link zum Volltext

Verfügbarkeit prüfen

A case report of the compression syndrome due to hypertrophic neuropathy

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

1991

Link zum Volltext

Verfügbarkeit prüfen

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

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

1989

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

Electrophysiological studies in siblings of De Sanctis-Cacchione syndrome

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

1989

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

Sweat function in Parkinson's disease

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

1994

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

Ceruletide therapy in action tremor following thalamic hemorrhage

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

1993

Link zum Volltext

Verfügbarkeit prüfen

Screaming during sleep in patients with Parkinson disease

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

1998

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

Central Motor Conductivity in Aged People

Internal Medicine, 1992, Vol.31(9), pp.1084-1087

1992

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 383

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(219)
Mit Volltextzugriff
(319)

Publikationsform

Sprache

Englisch
(299)
Japanisch
(195)
Deutsch
(2)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

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

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

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

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

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

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

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

An MRI study of hereditary spinocerebellar degenerations

A case of Japanese encephalitis demonstrating characteristic changes in MRI

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

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

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

Screaming during sleep in patients with Parkinson disease

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

Central Motor Conductivity in Aged People

Suchergebnisse filtern