UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Axonal swellings predict the degeneration of epidermal nerve fibers in painful neuropathies

Neurology, 2003-09, Vol.61 (5), p.631-636

2003

Volltextzugriff (PDF)

Epidermal nerve fiber density in sensory ganglionopathies: Clinical and neurophysiologic correlations

Muscle & nerve, 2001-08, Vol.24 (8), p.1034-1039

2001

Volltextzugriff (PDF)

Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation

Neurology, 2000-04, Vol.54 (8), p.1696-1698

2000

Volltextzugriff (PDF)

Sensory neuron diseases

Lancet neurology, 2005-06, Vol.4 (6), p.349-361

2005

Volltextzugriff (PDF)

Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion

Neurology, 1996-04, Vol.46 (4), p.1133-1137

1996

Volltextzugriff (PDF)

Impaired copper and iron metabolism in blood cells and muscles of patients affected by copper deficiency myeloneuropathy

Neuropathology and applied neurobiology, 2014-12, Vol.40 (7), p.888-898

2014

Volltextzugriff (PDF)

MR Imaging and Proton MR Spectroscopy in Adult Krabbe Disease

American journal of neuroradiology : AJNR, 2000-09, Vol.21 (8), p.1478-1482

2000

Volltextzugriff (PDF)

Imaging and outcome in severe complications of lumbar epidural anaesthesia : report of 16 cases

Neuroradiology, 2000-08, Vol.42 (8), p.564-571

2000

Volltextzugriff (PDF)

Chronic inflammatory demyelinating polyradiculoneuropathy: long-term course and treatment of 60 patients

Neurological sciences, 2000-02, Vol.21 (1), p.31-37

2000

Volltextzugriff (PDF)

Parenchymatous neurosyphilis

Neurological sciences, 2001-06, Vol.22 (3), p.281-282

2001

Volltextzugriff (PDF)

The insomnia plague: a Gabriel García Márquez story

Neurological sciences, 2000-08, Vol.21 (4), p.251-253

2000

Volltextzugriff (PDF)

Heterozygous Null Mutation in the P 0 Gene Associated with Mild Charcot-Marie-Tooth Disease

Annals of the New York Academy of Sciences, 1999-10, Vol.883 (1), p.477-480

1999

Volltextzugriff (PDF)

Charcot-Marie-Tooth disease type 2 and P0 gene mutations

Neurology, 1999-03, Vol.52 (5), p.1110

1999

Volltextzugriff (PDF)

Tubule and neurofilament immunoreactivity in human hairy skin: Markers for intraepidermal nerve fibers

Muscle & nerve, 2004-09, Vol.30 (3), p.310-316

2004

Volltextzugriff (PDF)

Spinal cord lesion due to epidural anesthesia

Neurological sciences, 2000-12, Vol.21 (6), p.411-412

2000

Volltextzugriff (PDF)

Azathioprine as a single drug or in combination with steroids in the treatment of myasthenia gravis

Journal of neurology, 1988-11, Vol.235 (8), p.449-453

1988

Volltextzugriff (PDF)

Clinical and magnetic resonance imaging findings in chronic sensory ganglionopathies

Annals of neurology, 2000-01, Vol.47 (1), p.104-109

2000

Volltextzugriff (PDF)

Deletion of exons 11-17 and novel mutations of the galactocerebrosidase gene in adult- and early-onset patients with Krabbe disease

Journal of neurology, 2000-11, Vol.247 (11), p.875-877

2000

Volltextzugriff (PDF)

Neurophysiological Diagnosis of Acquired Sensory Ganglionopathies

European neurology, 2003-01, Vol.50 (3), p.146-152

2003

Volltextzugriff (PDF)

HMSN III phenotype due to homozygous expression of a dominant HMSN II gene

Neurology, 1992-11, Vol.42 (11), p.2201-2201

1992

Volltextzugriff (PDF)

Acute treatment of myasthenia gravis with intranasal neostigmine: clinical and electromyographic evaluation

Journal of neurology, neurosurgery and psychiatry, 1991-12, Vol.54 (12), p.1061-1062

1991

Volltextzugriff (PDF)

"La toccatina": polyglottal aphasia in Pirandello

Italian journal of neurological sciences, 1997-02, Vol.18 (1), p.55-57

1997

Volltextzugriff (PDF)

Epidural anesthesia

Neurology, 1997-01, Vol.48 (1), p.293; author reply 294

1997

Volltextzugriff (PDF)

Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsies

Neurology, 1997-12, Vol.49 (6), p.1635-1640

1997

Volltextzugriff (PDF)

17p11.2 duplication is a common finding in sporadic cases of Charcot-Marie-Tooth type 1

European neurology, 1994, Vol.34 (3), p.135-139

1994

Volltextzugriff (PDF)

1 – 25 von 54

Suche als RSS-Feed

Aktive Filter

ThemaNeurosciences & Neurology

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(51)
Mit Volltextzugriff
(41)

Publikationsform

Artikel
(54)

Sprache

Englisch
(54)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(54)
Science & Technology
(54)
Clinical Neurology
(53)
Humans
(52)
Female
(35)
Adult
(34)
Neurosciences
(33)
Male
(31)
Middle Aged
(24)
Biological And Medical Sciences
(19)
Medical Sciences
(19)
Aged
(16)
Adolescent
(15)
Neurology
(15)
Magnetic Resonance Imaging
(12)
Child
(10)
Nervous System
(7)
Cranial Nerves. Spinal Roots. Peripheral Nerves. Autonomic Nervous System. Gustation. Olfaction
(6)
Hereditary Sensory And Motor Neuropathy - Genetics
(6)

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Axonal swellings predict the degeneration of epidermal nerve fibers in painful neuropathies

Epidermal nerve fiber density in sensory ganglionopathies: Clinical and neurophysiologic correlations

Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation

Sensory neuron diseases

Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion

Impaired copper and iron metabolism in blood cells and muscles of patients affected by copper deficiency myeloneuropathy

MR Imaging and Proton MR Spectroscopy in Adult Krabbe Disease

Imaging and outcome in severe complications of lumbar epidural anaesthesia : report of 16 cases

Chronic inflammatory demyelinating polyradiculoneuropathy: long-term course and treatment of 60 patients

Parenchymatous neurosyphilis

The insomnia plague: a Gabriel García Márquez story

Heterozygous Null Mutation in the P 0 Gene Associated with Mild Charcot-Marie-Tooth Disease

Charcot-Marie-Tooth disease type 2 and P0 gene mutations

Tubule and neurofilament immunoreactivity in human hairy skin: Markers for intraepidermal nerve fibers

Spinal cord lesion due to epidural anesthesia

Azathioprine as a single drug or in combination with steroids in the treatment of myasthenia gravis

Clinical and magnetic resonance imaging findings in chronic sensory ganglionopathies

Deletion of exons 11-17 and novel mutations of the galactocerebrosidase gene in adult- and early-onset patients with Krabbe disease

Neurophysiological Diagnosis of Acquired Sensory Ganglionopathies

HMSN III phenotype due to homozygous expression of a dominant HMSN II gene

Acute treatment of myasthenia gravis with intranasal neostigmine: clinical and electromyographic evaluation

"La toccatina": polyglottal aphasia in Pirandello

Epidural anesthesia

Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsies

17p11.2 duplication is a common finding in sporadic cases of Charcot-Marie-Tooth type 1

Aktive Filter

Suchergebnisse filtern