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...

Association study of calcitonin gene-related polypeptide-alpha (CALCA) gene polymorphism with migraine

Brain research, 2011-03, Vol.1378, p.119-124

2011

Volltextzugriff (PDF)

Survival in Medically Treated Patients with Homozygous β-Thalassemia

The New England journal of medicine, 1994-09, Vol.331 (9), p.574-578

1994

Volltextzugriff (PDF)

Association between migraine and a functional polymorphism at the dopamine β-hydroxylase locus

Neurogenetics, 2009-07, Vol.10 (3), p.199-208

2009

Volltextzugriff (PDF)

Characteristics of breast carcinomas missed by screening radiologists

Radiology, 1997-07, Vol.204 (1), p.131-135

1997

Volltextzugriff (PDF)

Further Investigation of the Predictors of Outcome Following First Schizophrenic Episodes

British journal of psychiatry, 1990-08, Vol.157 (2), p.182-189

1990

Volltextzugriff (PDF)

Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort

Neurogenetics, 2012-02, Vol.13 (1), p.97-101

2012

Volltextzugriff (PDF)

Pre-injury status and adaptation following traumatic brain injury

Brain injury, 2002, Vol.16 (1), p.41-49

2002

Volltextzugriff (PDF)

Majusculoic Acid, a Brominated Cyclopropyl Fatty Acid from a Marine Cyanobacterial Mat Assemblage

Journal of natural products (Washington, D.C.), 2005-04, Vol.68 (4), p.604-606

2005

Volltextzugriff (PDF)

Bevacizumab Diminishes Experimental Autoimmune Encephalomyelitis by Inhibiting Spinal Cord Angiogenesis and Reducing Peripheral T-Cell Responses

Journal of neuropathology and experimental neurology, 2012-11, Vol.71 (11), p.983-999

2012

Volltextzugriff (PDF)

Molecular cloning and characterization of the hblA gene encoding the B component of hemolysin BL from Bacillus cereus

Journal of Bacteriology, 1993-11, Vol.175 (21), p.6760-6766

1993

Volltextzugriff (PDF)

Huntingtin Protein Colocalizes with Lesions of Neurodegenerative Diseases: An Investigation in Huntington's, Alzheimer's, and Pick's Diseases

Experimental neurology, 1998-04, Vol.150 (2), p.213-222

1998

Volltextzugriff (PDF)

Adult onset Krabbe disease may mimic motor neurone disease

Journal of clinical neuroscience, 2003-09, Vol.10 (5), p.638-639

2003

Volltextzugriff (PDF)

Angiogenesis is Regulated by Angiopoietins During Experimental Autoimmune Encephalomyelitis and is Indirectly Related to Vascular Permeability

Journal of neuropathology and experimental neurology, 2011-12, Vol.70 (12), p.1107-1123

2011

Volltextzugriff (PDF)

Characterization of the components of hemolysin BL from Bacillus cereus

Infection and Immunity, 1991-05, Vol.59 (5), p.1778-1784

1991

Volltextzugriff (PDF)

Caminosides B-D, antimicrobial glycolipids isolated from the marine sponge Caminus sphaeroconia

Journal of natural products (Washington, D.C.), 2006-02, Vol.69 (2), p.173-177

2006

Volltextzugriff (PDF)

(2S,3R)-2-Aminododecan-3-ol, a New Antifungal Agent from the Ascidian Clavelina oblonga

Journal of natural products (Washington, D.C.), 2004-11, Vol.67 (11), p.1879-1881

2004

Volltextzugriff (PDF)

Microsomal epoxide hydrolase gene polymorphism and susceptibility to colon cancer

British journal of cancer, 1999-01, Vol.79 (1), p.168-171

1999

Volltextzugriff (PDF)

Successful mobilization of peripheral blood stem cells after addition of ancestim (stem cell factor) in patients who had failed a prior mobilization with filgrastim (granulocyte colony-stimulating factor) alone or with chemotherapy plus filgrastim

Bone marrow transplantation (Basingstoke), 2003-03, Vol.31 (5), p.371-378

2003

Volltextzugriff (PDF)

A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3

Journal of medical genetics, 2003-07, Vol.40 (7), p.515-519

2003

Volltextzugriff (PDF)

Molecular analysis and clinical correlations of the Huntington's disease mutation

The Lancet (British edition), 1993-10, Vol.342 (8877), p.954-958

1993

Volltextzugriff (PDF)

Partial Characterisation of Murine Huntingtin and Apparent Variations in the Subcellular Localisation of Huntingtin in Human, Mouse and Rat Brain

Human molecular genetics, 1996-04, Vol.5 (4), p.481-487

1996

Volltextzugriff (PDF)

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine

Neurogenetics, 2005-05, Vol.6 (2), p.67-72

2005

Volltextzugriff (PDF)

Mitochondrial DNA depletion: Prevalence in a pediatric population referred for neurologic evaluation

Pediatric neurology, 1996-04, Vol.14 (3), p.203-210

1996

Volltextzugriff (PDF)

Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twins

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2007-01, Vol.144B (1), p.95-100

2007

Volltextzugriff (PDF)

Neuropathological diagnosis and CAG repeat expansion in Huntington's disease

Journal of neurology, neurosurgery and psychiatry, 1996-01, Vol.60 (1), p.78-81

1996

Volltextzugriff (PDF)

1 – 25 von 365

Suche als RSS-Feed

Aktive Filter

ThemaChild

ThemaBiological And Medical Sciences

ThemaScience & Technology

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(342)
Mit Volltextzugriff
(310)

Publikationsform

Artikel
(363)
magazinearticle
(2)

Sprache

Englisch
(365)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(356)
Medical Sciences
(248)
Humans
(222)
Female
(172)
Male
(149)
Fundamental And Applied Biological Sciences. Psychology
(128)
Adult
(111)
Middle Aged
(100)
Animals
(74)
Aged
(70)
Tumors
(52)
Neurosciences & Neurology
(51)
Clinical Neurology
(41)
Oncology
(41)
Surgery
(40)
Pharmacology. Drug Treatments
(38)
Plant Sciences
(38)
Adolescent
(35)

13 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Association study of calcitonin gene-related polypeptide-alpha (CALCA) gene polymorphism with migraine

Survival in Medically Treated Patients with Homozygous β-Thalassemia

Association between migraine and a functional polymorphism at the dopamine β-hydroxylase locus

Characteristics of breast carcinomas missed by screening radiologists

Further Investigation of the Predictors of Outcome Following First Schizophrenic Episodes

Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort

Pre-injury status and adaptation following traumatic brain injury

Majusculoic Acid, a Brominated Cyclopropyl Fatty Acid from a Marine Cyanobacterial Mat Assemblage

Bevacizumab Diminishes Experimental Autoimmune Encephalomyelitis by Inhibiting Spinal Cord Angiogenesis and Reducing Peripheral T-Cell Responses

Molecular cloning and characterization of the hblA gene encoding the B component of hemolysin BL from Bacillus cereus

Huntingtin Protein Colocalizes with Lesions of Neurodegenerative Diseases: An Investigation in Huntington's, Alzheimer's, and Pick's Diseases

Adult onset Krabbe disease may mimic motor neurone disease

Angiogenesis is Regulated by Angiopoietins During Experimental Autoimmune Encephalomyelitis and is Indirectly Related to Vascular Permeability

Characterization of the components of hemolysin BL from Bacillus cereus

Caminosides B-D, antimicrobial glycolipids isolated from the marine sponge Caminus sphaeroconia

(2S,3R)-2-Aminododecan-3-ol, a New Antifungal Agent from the Ascidian Clavelina oblonga

Microsomal epoxide hydrolase gene polymorphism and susceptibility to colon cancer

Successful mobilization of peripheral blood stem cells after addition of ancestim (stem cell factor) in patients who had failed a prior mobilization with filgrastim (granulocyte colony-stimulating factor) alone or with chemotherapy plus filgrastim

A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3

Molecular analysis and clinical correlations of the Huntington's disease mutation

Partial Characterisation of Murine Huntingtin and Apparent Variations in the Subcellular Localisation of Huntingtin in Human, Mouse and Rat Brain

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine

Mitochondrial DNA depletion: Prevalence in a pediatric population referred for neurologic evaluation

Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twins

Neuropathological diagnosis and CAG repeat expansion in Huntington's disease

Aktive Filter

Suchergebnisse filtern