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...

Palmoplantar keratoderma and Charcot–Marie–Tooth disease: combination of two independent genetic diseases? Identification of two point mutations in the MPZ and KRT1 genes by whole‐exome sequencing

British journal of dermatology (1951), 2017-07, Vol.177 (1), p.284-286

2017

Volltextzugriff (PDF)

Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study

Neurology, 2006-04, Vol.66 (8), p.1207-1210

2006

Volltextzugriff (PDF)

Familial basilar migraine associated with a new mutation in the ATP1A2 gene

Neurology, 2005-12, Vol.65 (11), p.1826-1828

2005

Volltextzugriff (PDF)

Effect of the 50 bp deletion polymorphism in the SOD1 promoter on SOD1 mRNA levels in Italian ALS patients

Journal of the neurological sciences, 2012-02, Vol.313 (1), p.75-78

2012

Volltextzugriff (PDF)

Mitochondrial DNA haplogroups influence the therapeutic response to riboflavin in migraineurs

Neurology, 2009-05, Vol.72 (18), p.1588

2009

Volltextzugriff (PDF)

Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type

Neurology, 2004-01, Vol.62 (1), p.103-106

2004

Volltextzugriff (PDF)

Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum

Neurology, 2004-01, Vol.62 (2), p.262-268

2004

Volltextzugriff (PDF)

Myelinated retinal fibers in autosomal recessive spastic ataxia of Charlevoix-Saguenay

European journal of neurology, 2011-09, Vol.18 (9), p.1187-1190

2011

Volltextzugriff (PDF)

Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I–II loop

Journal of the neurological sciences, 2007-03, Vol.254 (1), p.69-71

2007

Volltextzugriff (PDF)

The wolframin His611Arg polymorphism influences medication overuse headache

Neuroscience letters, 2007-09, Vol.424 (3), p.179-184

2007

Volltextzugriff (PDF)

A Novel ATP1A2 Mutation in a Family with FHM Type II

Cephalalgia, 2006-03, Vol.26 (3), p.324-328

2006

Volltextzugriff (PDF)

Skeletal muscle wasting in tumor-bearing rats is associated with MyoD down-regulation

International journal of oncology, 2005-06, Vol.26 (6), p.1663

2005

Volltextzugriff (PDF)

The Sygen® multicenter acute Spinal cord injury study

Spine (Philadelphia, Pa. 1976), 2001-12, Vol.26 (24), p.S87-S100

2001

Volltextzugriff (PDF)

Measurements and recovery patterns in a multicenter study of acute Spinal cord injury

Spine (Philadelphia, Pa. 1976), 2001-12, Vol.26 (24), p.S68-S86

2001

Volltextzugriff (PDF)

Risk of myocardial infarction and angina in patients with severe peripheral vascular disease: Predictive role of C-reactive protein

Circulation (New York, N.Y.), 2002-02, Vol.105 (7), p.800-803

2002

Volltextzugriff (PDF)

CAG Repeat Expansion in an Italian Family with Spinocerebellar Ataxia Type 2 (SCA2): A Clinical and Genetic Study

European neurology, 1998-10, Vol.40 (3), p.164-168

1998

Volltextzugriff (PDF)

Recruitment and early treatment in a multicenter study of Acute spinal cord injury

Spine (Philadelphia, Pa. 1976), 2001-12, Vol.26 (24), p.S58-S67

2001

Volltextzugriff (PDF)

Ventricular aneurysm due to blunt chest injury

The Annals of thoracic surgery, 1989-02, Vol.47 (2), p.322-329

1989

Volltextzugriff (PDF)

Effects of simvastatin administration in an experimental model of cancer cachexia

Nutrition (Burbank, Los Angeles County, Calif.), 2003-11, Vol.19 (11), p.936-939

2003

Volltextzugriff (PDF)

Early Myocardial Revascularization for Postinfarction Angina

The Annals of thoracic surgery, 1987-08, Vol.44 (2), p.159-163

1987

Volltextzugriff (PDF)

Evaluating neuroprotective agents for clinical anti-ischemic benefit using neurological and neuropsychological changes after cardiac surgery under cardiopulmonary bypass : Methodological strategies and results of a double-blind, placebo-controlled trial of GM1 ganglioside

Stroke (1970), 1996-05, Vol.27 (5), p.858-874

1996

Volltextzugriff (PDF)

Multicentre Italian family-based association study on tyrosine hydroxylase, catechol-O-methyl transferase and Wolfram syndrome 1 polymorphisms in mood disorders

Psychiatric genetics, 2003-06, Vol.13 (2), p.121-126

2003

Volltextzugriff (PDF)

Pacing lead fracture after a deceleration injury

The Annals of thoracic surgery, 1989-03, Vol.47 (3), p.453-454

1989

Volltextzugriff (PDF)

The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome

Journal of neurology, neurosurgery and psychiatry, 1996-07, Vol.61 (1), p.47-51

1996

Volltextzugriff (PDF)

Association in the same patient of autosomal dominant progressive external ophthalmoplegia with multiple mtDNA deletions and X-linked ichthyosis: clinical, biochemical, histological, submicroscopic and molecular genetic study

Journal of submicroscopic cytology and pathology, 1998-10, Vol.30 (4), p.521

1998

Volltextzugriff (PDF)

1 – 25 von 222

Suche als RSS-Feed

Aktive Filter

ThemaMale

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(175)
Mit Volltextzugriff
(137)

Publikationsform

Artikel
(222)

Sprache

Englisch
(194)
Italienisch
(29)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Palmoplantar keratoderma and Charcot–Marie–Tooth disease: combination of two independent genetic diseases? Identification of two point mutations in the MPZ and KRT1 genes by whole‐exome sequencing

Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study

Familial basilar migraine associated with a new mutation in the ATP1A2 gene

Effect of the 50 bp deletion polymorphism in the SOD1 promoter on SOD1 mRNA levels in Italian ALS patients

Mitochondrial DNA haplogroups influence the therapeutic response to riboflavin in migraineurs

Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type

Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum

Myelinated retinal fibers in autosomal recessive spastic ataxia of Charlevoix-Saguenay

Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I–II loop

The wolframin His611Arg polymorphism influences medication overuse headache

A Novel ATP1A2 Mutation in a Family with FHM Type II

Skeletal muscle wasting in tumor-bearing rats is associated with MyoD down-regulation

The Sygen® multicenter acute Spinal cord injury study

Measurements and recovery patterns in a multicenter study of acute Spinal cord injury

Risk of myocardial infarction and angina in patients with severe peripheral vascular disease: Predictive role of C-reactive protein

CAG Repeat Expansion in an Italian Family with Spinocerebellar Ataxia Type 2 (SCA2): A Clinical and Genetic Study

Recruitment and early treatment in a multicenter study of Acute spinal cord injury

Ventricular aneurysm due to blunt chest injury

Effects of simvastatin administration in an experimental model of cancer cachexia

Early Myocardial Revascularization for Postinfarction Angina

Evaluating neuroprotective agents for clinical anti-ischemic benefit using neurological and neuropsychological changes after cardiac surgery under cardiopulmonary bypass : Methodological strategies and results of a double-blind, placebo-controlled trial of GM1 ganglioside

Multicentre Italian family-based association study on tyrosine hydroxylase, catechol-O-methyl transferase and Wolfram syndrome 1 polymorphisms in mood disorders

Pacing lead fracture after a deceleration injury

The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome

Association in the same patient of autosomal dominant progressive external ophthalmoplegia with multiple mtDNA deletions and X-linked ichthyosis: clinical, biochemical, histological, submicroscopic and molecular genetic study

Aktive Filter

Suchergebnisse filtern