UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 725

Sortiert nach

High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2

Neurology, 1999-06, Vol.52 (9), p.1816

1999

Volltextzugriff (PDF)

Phenotypic variability of aprataxin gene mutations

Neurology, 2003-03, Vol.60 (5), p.868

2003

Volltextzugriff (PDF)

Homozygosity mapping of Marinesco-Sjögren syndrome to 5q31

European journal of human genetics : EJHG, 2003-10, Vol.11 (10), p.770-778

2003

Volltextzugriff (PDF)

Clinical and molecular features of spinocerebellar ataxia type 6

Neurology, 1997-11, Vol.49 (5), p.1243

1997

Volltextzugriff (PDF)

Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation

Neurology, 2000-03, Vol.54 (5), p.1075

2000

Volltextzugriff (PDF)

Unusual Phenotypic Alteration of β Amyloid Precursor Protein (β APP) Maturation by a New Val-715 → Met β APP-770 Mutation Responsible for Probable Early-Onset Alzheimer's Disease

Proceedings of the National Academy of Sciences - PNAS, 1999-03, Vol.96 (7), p.4119-4124

1999

Volltextzugriff (PDF)

Factors associated to hypermanganesemia in patients receiving home parenteral nutrition

Clinical nutrition (Edinburgh, Scotland), 2000-10, Vol.19 (5), p.343-348

2000

Volltextzugriff (PDF)

La maladie de Lyme

Revue neurologique, 2003, Vol.159 (1), p.23-30

2003

Volltextzugriff (PDF)

Novel muscle chloride channel (CLCN1) mutations in myotonia congenita with various modes of inheritance including incomplete dominance and penetrance

Neurology, 1998-04, Vol.50 (4), p.1176

1998

Volltextzugriff (PDF)

Characterization of new polyclonal antibodies specific for 40 and 42 amino acid-long amyloid beta peptides: their use to examine the cell biology of presenilins and the immunohistochemistry of sporadic Alzheimer's disease and cerebral amyloid angiopathy cases

Molecular medicine (Cambridge, Mass.), 1997-10, Vol.3 (10), p.695-707

1997

Volltextzugriff (PDF)

Constitutive muscular abnormalities in culture in spinal muscular atrophy

The Lancet (British edition), 1995-03, Vol.345 (8951), p.694-695

1995

Volltextzugriff (PDF)

L’interféron β1-a IM ne modifie pas le fonctionnement psychologique global de patients atteints de sclérose en plaques rémittente pendant les premiers mois de traitement

Revue neurologique, 2005-12, Vol.161 (12), p.1197-1204

2005

Volltextzugriff (PDF)

Is clonidine growth hormone stimulation a good test to differentiate multiple system atrophy from idiopathic Parkinson's disease?

Journal of neurology, 2000-11, Vol.247 (11), p.853-856

2000

Volltextzugriff (PDF)

Basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

Neurology, 1999-04, Vol.52 (6), p.1244

1999

Volltextzugriff (PDF)

Mapk Activation Via 5-Hydroxytryptamine 1A Receptor is Involved in the Neuroprotective Effects of Xaliproden

International journal of immunopathology and pharmacology, 2005-01, Vol.18 (1), p.21-31

2005

Volltextzugriff (PDF)

Effect of the nonpeptide neurotrophic compound SR 57746A on the phenotypic survival of purified mouse motoneurons

British journal of pharmacology, 1999-12, Vol.128 (7), p.1385-1392

1999

Volltextzugriff (PDF)

Prednisolone enhances myogenesis and dystrophin-related protein in skeletal muscle cell cultures from mdx mouse

Journal of neuroscience research, 1993-07, Vol.35 (4), p.363-372

1993

Volltextzugriff (PDF)

Muscle could be the therapeutic target in SMA treatment

Journal of neuroscience research, 1998-09, Vol.53 (6), p.663-669

1998

Volltextzugriff (PDF)

Maladies neurologiques héréditaires dues à l'amplification de la répétition d'un triplet

La Presse médicale (1983), 1998-02, Vol.27 (8), p.376-381

1998

Volltextzugriff (PDF)

A 7-kDa Prion Protein (PrP) Fragment, an Integral Component of the PrP Region Required for Infectivity, Is the Major Amyloid Protein in Gerstmann-Sträussler-Scheinker Disease A117V

The Journal of biological chemistry, 2001-02, Vol.276 (8), p.6009-6015

2001

Volltextzugriff (PDF)

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

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

1990

Volltextzugriff (PDF)

Neurotrophins increase motoneurons' ability to innervate skeletal muscle fibers in rat spinal cord-human muscle cocultures

Journal of the neurological sciences, 1996-03, Vol.136 (1), p.17-23

1996

Volltextzugriff (PDF)

Spontaneous spike and wave discharges in thalamus and cortex in a rat model of genetic petit mal-like seizures

Experimental neurology, 1987-04, Vol.96 (1), p.127-136

1987

Volltextzugriff (PDF)

Neurofibrillary tangles in Gerstmann-Sträussler-Scheinker syndrome with the A117V prion gene mutation

Journal of neurology, neurosurgery and psychiatry, 1997-08, Vol.63 (2), p.240-246

1997

Volltextzugriff (PDF)

Compensatory mechanism of motor defect in SOD1 transgenic mice by overactivation of striatal cholinergic neurons

Neuroreport, 1999-04, Vol.10 (5), p.1013-1018

1999

Volltextzugriff (PDF)

1 – 25 von 725

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(412)
Mit Volltextzugriff
(299)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2

Phenotypic variability of aprataxin gene mutations

Homozygosity mapping of Marinesco-Sjögren syndrome to 5q31

Clinical and molecular features of spinocerebellar ataxia type 6

Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation

Unusual Phenotypic Alteration of β Amyloid Precursor Protein (β APP) Maturation by a New Val-715 → Met β APP-770 Mutation Responsible for Probable Early-Onset Alzheimer's Disease

Factors associated to hypermanganesemia in patients receiving home parenteral nutrition

La maladie de Lyme

Novel muscle chloride channel (CLCN1) mutations in myotonia congenita with various modes of inheritance including incomplete dominance and penetrance

Characterization of new polyclonal antibodies specific for 40 and 42 amino acid-long amyloid beta peptides: their use to examine the cell biology of presenilins and the immunohistochemistry of sporadic Alzheimer's disease and cerebral amyloid angiopathy cases

Constitutive muscular abnormalities in culture in spinal muscular atrophy

L’interféron β1-a IM ne modifie pas le fonctionnement psychologique global de patients atteints de sclérose en plaques rémittente pendant les premiers mois de traitement

Is clonidine growth hormone stimulation a good test to differentiate multiple system atrophy from idiopathic Parkinson's disease?

Basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

Mapk Activation Via 5-Hydroxytryptamine 1A Receptor is Involved in the Neuroprotective Effects of Xaliproden

Effect of the nonpeptide neurotrophic compound SR 57746A on the phenotypic survival of purified mouse motoneurons

Prednisolone enhances myogenesis and dystrophin-related protein in skeletal muscle cell cultures from mdx mouse

Muscle could be the therapeutic target in SMA treatment

Maladies neurologiques héréditaires dues à l'amplification de la répétition d'un triplet

A 7-kDa Prion Protein (PrP) Fragment, an Integral Component of the PrP Region Required for Infectivity, Is the Major Amyloid Protein in Gerstmann-Sträussler-Scheinker Disease A117V

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

Neurotrophins increase motoneurons' ability to innervate skeletal muscle fibers in rat spinal cord-human muscle cocultures

Spontaneous spike and wave discharges in thalamus and cortex in a rat model of genetic petit mal-like seizures

Neurofibrillary tangles in Gerstmann-Sträussler-Scheinker syndrome with the A117V prion gene mutation

Compensatory mechanism of motor defect in SOD1 transgenic mice by overactivation of striatal cholinergic neurons

Suchergebnisse filtern