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...

Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease

Neurology, 2004-08, Vol.63 (3), p.443-449

2004

Volltextzugriff (PDF)

Less protease-resistant PrP in a patient with sporadic CJD treated with intraventricular pentosan polysulphate

Acta neurologica Scandinavica, 2010-02, Vol.121 (2), p.127-130

2010

Volltextzugriff (PDF)

Cerebroventricular infusion of pentosan polysulphate in human variant Creutzfeldt–Jakob disease

The Journal of infection, 2005-06, Vol.50 (5), p.394-396

2005

Volltextzugriff (PDF)

Clusterin expression in follicular dendritic cells associated with prion protein accumulation

The Journal of pathology, 2006-08, Vol.209 (4), p.484-491

2006

Volltextzugriff (PDF)

Fatal familial insomnia with an unusual prion protein deposition pattern: an autopsy report with an experimental transmission study

Neuropathology and applied neurobiology, 2005-02, Vol.31 (1), p.80-87

2005

Volltextzugriff (PDF)

Experimental treatments for human transmissible spongiform encephalopathies: is there a role for pentosan polysulfate?

Expert opinion on biological therapy, 2007-05, Vol.7 (5), p.713-726

2007

Volltextzugriff (PDF)

Clinical features of Creutzfeldt-Jakob disease with V180I mutation

Neurology, 2004-02, Vol.62 (3), p.502-505

2004

Volltextzugriff (PDF)

Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution

Journal of neurology, 2007-11, Vol.254 (11), p.1509-1517

2007

Volltextzugriff (PDF)

Lysosomotropic Agents and Cysteine Protease Inhibitors Inhibit Scrapie-Associated Prion Protein Accumulation

Journal of Virology, 2000-05, Vol.74 (10), p.4894-4897

2000

Volltextzugriff (PDF)

Treatment of Transmissible Spongiform Encephalopathy by Intraventricular Drug Infusion in Animal Models

Journal of Virology, 2004-05, Vol.78 (10), p.4999-5006

2004

Volltextzugriff (PDF)

Protein aggregation

Journal of the neurological sciences, 2017-10, Vol.381, p.31-31

Doh-ura, K.

2017

Volltextzugriff (PDF)

Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease

Journal of Virology, 1991-11, Vol.65 (11), p.6292-6295

1991

Volltextzugriff (PDF)

Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt- Jakob disease

The American journal of pathology, 1992-06, Vol.140 (6), p.1285-1294

1992

Volltextzugriff (PDF)

Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Sträussler-Scheinker syndrome

Neurology, 1990-10, Vol.40 (10), p.1578-1578

1990

Volltextzugriff (PDF)

Japanese family with parkinsonism, depression, weight loss, and central hypoventilation

Neurology, 2002-04, Vol.58 (7), p.1025-1030

2002

Volltextzugriff (PDF)

CJD discrepancy

Nature (London), 1991-10, Vol.353 (6347), p.801-802

1991

Volltextzugriff (PDF)

Quinoline Derivatives Are Therapeutic Candidates for Transmissible Spongiform Encephalopathies

Journal of Virology, 2004-02, Vol.78 (3), p.1281-1288

2004

Volltextzugriff (PDF)

Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia

Journal of neurology, neurosurgery and psychiatry, 2000-03, Vol.68 (3), p.388-388

2000

Volltextzugriff (PDF)

Clusterin/apolipoprotein J is associated with cortical Lewy bodies: immunohistochemical study in cases with α-synucleinopathies

Acta neuropathologica, 2002-09, Vol.104 (3), p.225-230

2002

Volltextzugriff (PDF)

Amyloid imaging probes are useful for detection of prion plaques and treatment of transmissible spongiform encephalopathies

Journal of general virology, 2004-06, Vol.85 (6), p.1785-1790

2004

Volltextzugriff (PDF)

Clustering of three cases of Creutzfeldt-Jakob disease near Fukuoka City, Japan

Acta neurologica Scandinavica, 1991-11, Vol.84 (5), p.445-447

1991

Volltextzugriff (PDF)

Current topics of Prion disease

Uirusu, 2001/12/30, Vol.51(2), pp.151-158

2001

Volltextzugriff (PDF)

Involvement of cathepsin B in the motor neuron degeneration of amyotrophic lateral sclerosis

Acta neuropathologica, 2003-05, Vol.105 (5), p.462-468

2003

Volltextzugriff (PDF)

A comparative immunohistochemical study of Kuru and senile plaques with a special reference to glial reactions at various stages of amyloid plaque formation

The American journal of pathology, 1991-09, Vol.139 (3), p.589-598

1991

Volltextzugriff (PDF)

The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system

The American journal of pathology, 1992-08, Vol.141 (2), p.271-277

1992

Volltextzugriff (PDF)

1 – 25 von 83

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(76)
Mit Volltextzugriff
(62)

Publikationsform

Artikel
(79)
Buchkapitel
(4)

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(66)
Science & Technology
(64)
Life Sciences & Biomedicine
(63)
Biological And Medical Sciences
(40)
Male
(39)
Neurosciences & Neurology
(39)
Clinical Neurology
(38)
Medical Sciences
(36)
Middle Aged
(35)
Female
(34)
Neurology
(31)
Pathology
(27)
Aged
(26)
Neurosciences
(26)
Immunohistochemistry
(24)
Animals
(22)
Prions - Genetics
(22)
Adult
(18)
Creutzfeldt-Jakob Syndrome - Pathology
(18)
Creutzfeldt-Jakob Disease
(16)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease

Less protease-resistant PrP in a patient with sporadic CJD treated with intraventricular pentosan polysulphate

Cerebroventricular infusion of pentosan polysulphate in human variant Creutzfeldt–Jakob disease

Clusterin expression in follicular dendritic cells associated with prion protein accumulation

Fatal familial insomnia with an unusual prion protein deposition pattern: an autopsy report with an experimental transmission study

Experimental treatments for human transmissible spongiform encephalopathies: is there a role for pentosan polysulfate?

Clinical features of Creutzfeldt-Jakob disease with V180I mutation

Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution

Lysosomotropic Agents and Cysteine Protease Inhibitors Inhibit Scrapie-Associated Prion Protein Accumulation

Treatment of Transmissible Spongiform Encephalopathy by Intraventricular Drug Infusion in Animal Models

Protein aggregation

Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease

Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt- Jakob disease

Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Sträussler-Scheinker syndrome

Japanese family with parkinsonism, depression, weight loss, and central hypoventilation

CJD discrepancy

Quinoline Derivatives Are Therapeutic Candidates for Transmissible Spongiform Encephalopathies

Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia

Clusterin/apolipoprotein J is associated with cortical Lewy bodies: immunohistochemical study in cases with α-synucleinopathies

Amyloid imaging probes are useful for detection of prion plaques and treatment of transmissible spongiform encephalopathies

Clustering of three cases of Creutzfeldt-Jakob disease near Fukuoka City, Japan

Current topics of Prion disease

Involvement of cathepsin B in the motor neuron degeneration of amyotrophic lateral sclerosis

A comparative immunohistochemical study of Kuru and senile plaques with a special reference to glial reactions at various stages of amyloid plaque formation

The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system

Suchergebnisse filtern