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...

Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron Degeneration

American journal of human genetics, 2008-02, Vol.82 (2), p.510-515

2008

Volltextzugriff (PDF)

Successful utilization of the EMR in a multiple sclerosis clinic to support quality improvement and research initiatives at the point of care

Multiple sclerosis journal - experimental, translational and clinical, 2018-10, Vol.4 (4), p.2055217318813736-2055217318813736

2018

Volltextzugriff (PDF)

Motor Neuron Degeneration in Mice That Express a Human Cu,Zn Superoxide Dismutase Mutation

Science (American Association for the Advancement of Science), 1994-06, Vol.264 (5166), p.1772-1775

1994

Volltextzugriff (PDF)

VZV encephalitis that developed in an immunized patient during fingolimod therapy

Neurology, 2015-01, Vol.84 (1), p.99-100

2015

Volltextzugriff (PDF)

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35

Nature genetics, 1994-07, Vol.7 (3), p.425-428

1994

Volltextzugriff (PDF)

Correlation Analysis of MRI Lesion Load and Clinical Measures in Multiple Sclerosis Cohort Using Structured Clinical Documentation Support Toolkit (1880)

Neurology, 2020-04, Vol.94 (15_supplement)

2020

Volltextzugriff (PDF)

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

Nature genetics, 2001-10, Vol.29 (2), p.160-165

2001

Volltextzugriff (PDF)

Amyotrophic Lateral Sclerosis and Structural Defects in Cu,Zn Superoxide Dismutase

Science (American Association for the Advancement of Science), 1993-08, Vol.261 (5124), p.1047-1051

1993

Volltextzugriff (PDF)

Molecular genetic basis of familial ALS

Neurology, 1996-10, Vol.47 (4 Suppl 2), p.S27

1996

Volltextzugriff (PDF)

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers

Neurogenetics, 1998-12, Vol.2 (1), p.55-60

1998

Volltextzugriff (PDF)

Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron Degeneration

American journal of human genetics, 2008-02, Vol.82 (2), p.24

2008

Volltextzugriff (PDF)

Human α-tocopherol transfer protein: Gene structure and mutations in familial vitamin E deficiency

Annals of neurology, 1996-03, Vol.39 (3), p.295-300

1996

Volltextzugriff (PDF)

Amyotrophic Lateral Ssclerosis and Structural Defects in Cu,Zn Superoxide Dismutase

Science (American Association for the Advancement of Science), 1993-08, Vol.261 (5124), p.1047-1051

1993

Volltextzugriff (PDF)

Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers

Human molecular genetics, 1994, Vol.3 (10), p.1867-1871

1994

Volltextzugriff (PDF)

Linkage of Scapuloperoneal Spinal Muscular Atrophy to Chromosome 12q24.1-q24.31

Human molecular genetics, 1996-09, Vol.5 (9), p.1377-1382

1996

Volltextzugriff (PDF)

Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosis

Human molecular genetics, 1995-06, Vol.4 (6), p.1113-1116

1995

Volltextzugriff (PDF)

Clinical and genetic heterogeneity of Charcot-Marie-Tooth disease

Genomics (San Diego, Calif.), 1992, Vol.12 (1), p.155-157

1992

Volltextzugriff (PDF)

Amyotropic lateral sclerosis and structural defects in Cu, Zn superoxide dismutase

Science (American Association for the Advancement of Science), 1993-08, Vol.261 (5124), p.1047

1993

Volltextzugriff (PDF)

1 – 19 von 19

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(19)
Mit Volltextzugriff
(16)

Publikationsform

Artikel
(19)

Sprache

Englisch
(19)
Japanisch
(1)

Erscheinungsjahr

n.n

Thema

Humans
(14)
Science & Technology
(13)
Biological And Medical Sciences
(11)
Life Sciences & Biomedicine
(10)
Medical Sciences
(9)
Neurology
(9)
Female
(8)
Male
(8)
Pedigree
(8)
Amyotrophic Lateral Sclerosis
(7)
Amyotrophic Lateral Sclerosis - Genetics
(7)
Genetics & Heredity
(7)
Mutation
(7)
Base Sequence
(6)
Chromosome Mapping
(6)
Molecular Sequence Data
(6)
Genetic Linkage
(5)
Lod Score
(5)
Man
(5)
Superoxide Dismutase
(5)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron Degeneration

Successful utilization of the EMR in a multiple sclerosis clinic to support quality improvement and research initiatives at the point of care

Motor Neuron Degeneration in Mice That Express a Human Cu,Zn Superoxide Dismutase Mutation

VZV encephalitis that developed in an immunized patient during fingolimod therapy

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35

Correlation Analysis of MRI Lesion Load and Clinical Measures in Multiple Sclerosis Cohort Using Structured Clinical Documentation Support Toolkit (1880)

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

Amyotrophic Lateral Sclerosis and Structural Defects in Cu,Zn Superoxide Dismutase

Molecular genetic basis of familial ALS

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers

Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron Degeneration

Human α-tocopherol transfer protein: Gene structure and mutations in familial vitamin E deficiency

Amyotrophic Lateral Ssclerosis and Structural Defects in Cu,Zn Superoxide Dismutase

Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers

Linkage of Scapuloperoneal Spinal Muscular Atrophy to Chromosome 12q24.1-q24.31

Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosis

Clinical and genetic heterogeneity of Charcot-Marie-Tooth disease

Amyotropic lateral sclerosis and structural defects in Cu, Zn superoxide dismutase

Suchergebnisse filtern