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...

Review: Somatic mutations in neurodegeneration

Neuropathology and applied neurobiology, 2018-04, Vol.44 (3), p.267-285

2018

Volltextzugriff (PDF)

Genetics of Parkinson's disease: alpha-synuclein and other insights from Greece

European journal of neurology, 2014-07, Vol.21 (7), p.946-947

Proukakis, C.

2014

Volltextzugriff (PDF)

Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia

American journal of human genetics, 2003-11, Vol.73 (5), p.1147-1156

2003

Volltextzugriff (PDF)

Genetics of P arkinson's disease: alpha‐synuclein and other insights from G reece

European journal of neurology, 2014-07, Vol.21 (7), p.946-947

Proukakis, C.

2014

Volltextzugriff (PDF)

Evolution and clustering of prodromal parkinsonian features in GBA1 carriers

Movement disorders, 2019-09, Vol.34 (9), p.1365-1373

2019

Volltextzugriff (PDF)

Modeling and estimation of ambiguities in linear arrays

IEEE transactions on signal processing, 1998-08, Vol.46 (8), p.2166-2179

1998

Volltextzugriff (PDF)

Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype

Clinical genetics, 2009-05, Vol.75 (5), p.485-489

2009

Volltextzugriff (PDF)

Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) gene

Human mutation, 2003-02, Vol.21 (2), p.170-170

2003

Volltextzugriff (PDF)

Is the Transportation Highway the Right Road for Hereditary Spastic Paraplegia?

American journal of human genetics, 2002-11, Vol.71 (5), p.1009-1016

2002

Volltextzugriff (PDF)

Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase

Nature genetics, 2004-11, Vol.36 (11), p.1225-1229

2004

Volltextzugriff (PDF)

Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome

Nature genetics, 2004-03, Vol.36 (3), p.271-276

2004

Volltextzugriff (PDF)

A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members

Journal of neurology, neurosurgery and psychiatry, 2001-12, Vol.71 (6), p.788-791

2001

Volltextzugriff (PDF)

Investigative study of planar array ambiguities based on "hyperhelical" parameterization

IEEE transactions on signal processing, 1999-06, Vol.47 (6), p.1532-1541

1999

Volltextzugriff (PDF)

SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia

Nature genetics, 2002-08, Vol.31 (4), p.347-348

2002

Volltextzugriff (PDF)

The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegia

Genomics (San Diego, Calif.), 2003-04, Vol.81 (4), p.437-441

2003

Volltextzugriff (PDF)

Human spastin has multiple microtubule‐related functions

Journal of neurochemistry, 2005-12, Vol.95 (5), p.1411-1420

2005

Volltextzugriff (PDF)

073 Hereditary spastic paraplegia caused by spastin (SPAST, SPG4) mutations is found more often in males: report of novel mutations from one centre, and review of published literature

Journal of neurology, neurosurgery and psychiatry, 2012-03, Vol.83 (3), p.e1-e1

2012

Volltextzugriff (PDF)

Infecton: a 99mTc-ciprofloxacin radiopharmaceutical for the detection of bone infection

Clinical microbiology and infection, 2003-02, Vol.9 (2), p.101-109

2003

Volltextzugriff (PDF)

Troyer syndrome revisited: A clinical and radiological study of a complicated hereditary spastic paraplegia

Journal of neurology, 2004-09, Vol.251 (9), p.1105-1110

2004

Volltextzugriff (PDF)

Experimental Study of the Response of Cup-type Radon Dosemeters

Radiation protection dosimetry, 1999-07, Vol.83 (3), p.263-266

1999

Volltextzugriff (PDF)

Bone Mineral Content of Junior Competitive Weightlifters

International journal of sports medicine, 1990-06, Vol.11 (3), p.244-246

1990

Volltextzugriff (PDF)

Thyroid function in postmenopausal women with breast cancer on tamoxifen

European journal of gynaecological oncology, 1998, Vol.19 (2), p.150

1998

Volltextzugriff (PDF)

Quality Control in Dental Radiology in Greece

Radiation protection dosimetry, 1998-01, Vol.80 (1-3), p.89-93

1998

Volltextzugriff (PDF)

Differences in effective dose estimation from dose-area product and entrance surface dose measurements in intravenous urography

British journal of radiology, 2001-08, Vol.74 (884), p.727-734

2001

Volltextzugriff (PDF)

Indoor Gamma Radiation Measurements in Greece

Radiation protection dosimetry, 1995-01, Vol.60 (2), p.177-180

1995

Volltextzugriff (PDF)

1 – 25 von 133

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(108)
Mit Volltextzugriff
(102)

Publikationsform

Artikel
(130)
Tagungsberichte
(3)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(94)
Life Sciences & Biomedicine
(58)
Humans
(57)
Biological And Medical Sciences
(43)
Female
(40)
Medical Sciences
(39)
Physics
(36)
Physical Sciences
(33)
Male
(30)
Adult
(24)
Optics
(24)
Middle Aged
(23)
Physics, Atomic, Molecular & Chemical
(20)
Radiology, Nuclear Medicine & Medical Imaging
(16)
Aged
(14)
Animals
(12)
Investigative Techniques, Diagnostic Techniques
(11)
Technology
(11)
Exact Sciences And Technology
(10)
Mice
(10)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Review: Somatic mutations in neurodegeneration

Genetics of Parkinson's disease: alpha-synuclein and other insights from Greece

Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia

Genetics of P arkinson's disease: alpha‐synuclein and other insights from G reece

Evolution and clustering of prodromal parkinsonian features in GBA1 carriers

Modeling and estimation of ambiguities in linear arrays

Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype

Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) gene

Is the Transportation Highway the Right Road for Hereditary Spastic Paraplegia?

Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase

Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome

A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members

Investigative study of planar array ambiguities based on "hyperhelical" parameterization

SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia

The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegia

Human spastin has multiple microtubule‐related functions

073 Hereditary spastic paraplegia caused by spastin (SPAST, SPG4) mutations is found more often in males: report of novel mutations from one centre, and review of published literature

Infecton: a 99mTc-ciprofloxacin radiopharmaceutical for the detection of bone infection

Troyer syndrome revisited: A clinical and radiological study of a complicated hereditary spastic paraplegia

Experimental Study of the Response of Cup-type Radon Dosemeters

Bone Mineral Content of Junior Competitive Weightlifters

Thyroid function in postmenopausal women with breast cancer on tamoxifen

Quality Control in Dental Radiology in Greece

Differences in effective dose estimation from dose-area product and entrance surface dose measurements in intravenous urography

Indoor Gamma Radiation Measurements in Greece

Suchergebnisse filtern