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...

Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C

Neurology, 2003-01, Vol.60 (1), p.22-26

2003

Volltextzugriff (PDF)

The clinical and genetic spectrum of spinocerebellar ataxia 14

Neurology, 2005-04, Vol.64 (7), p.1258-1260

2005

Volltextzugriff (PDF)

Late-onset hereditary axonal neuropathies

Neurology, 2008-07, Vol.71 (1), p.14-20

2008

Volltextzugriff (PDF)

Charcot–Marie–Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genes

Neuromuscular disorders : NMD, 2002-10, Vol.12 (7), p.643-650

2002

Volltextzugriff (PDF)

Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: A 20-year study

Annals of neurology, 1997-04, Vol.41 (4), p.463-469

1997

Volltextzugriff (PDF)

Familial spastic paraparesis: Evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2

American journal of medical genetics, 1997-02, Vol.74 (1), p.26-36

1997

Volltextzugriff (PDF)

Impotence associated with the Charcot-Marie-Tooth syndrome

European neurology, 1994, Vol.34 (3), p.155-157

1994

Volltextzugriff (PDF)

Severe vincristine neuropathy in charcot‐marie‐tooth disease type 1A

Cancer, 1996-04, Vol.77 (7), p.1356-1362

1996

Volltextzugriff (PDF)

Cerebral cavernous malformation: novel mutation in a Chinese family and evidence for heterogeneity

Journal of the neurological sciences, 2002-04, Vol.196 (1), p.91-96

2002

Volltextzugriff (PDF)

The use of apolipoprotein CII as a genetic marker for myotonic dystrophy

Archives of neurology (Chicago), 1987-03, Vol.44 (3), p.273-275

1987

Volltextzugriff (PDF)

The Consequences of Testing for Huntington's Disease

The New England journal of medicine, 1993-04, Vol.328 (14), p.1046-1046

1993

Volltextzugriff (PDF)

Prevention of nervous system trauma from travel in motor vehicles

Journal of neurosurgical nursing, 1985-04, Vol.17 (2), p.77-82

Lipe, H P

1985

Volltextzugriff (PDF)

The neuro nurse specialist--present and future considerations

Journal of neurosurgical nursing, 1983-10, Vol.15 (5), p.317-319

1983

Volltextzugriff (PDF)

Positioning the patient with intracranial hypertension: how turning and head rotation affect the internal jugular vein

Heart & lung, 1980-11, Vol.9 (6), p.1031-1037

1980

Volltextzugriff (PDF)

Double trouble in hereditary neuropathy: concomitant mutations in the PMP-22 gene and another gene produce novel phenotypes

Archives of neurology (Chicago), 2006-01, Vol.63 (1), p.112

2006

Volltextzugriff (PDF)

Impact of presymptomatic genetic testing for hereditary ataxia and neuromuscular disorders

Archives of neurology (Chicago), 2004-06, Vol.61 (6), p.875

2004

Volltextzugriff (PDF)

Severe vincristine neuropathy in Charcot-Marie-Tooth diseae type 1A

Cancer, 1996, Vol.77 (7), p.1356-1362

1996

Volltextzugriff (PDF)

Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders: Where is the Evidence?—Reply

Archives of neurology (Chicago), 2005-01, Vol.62 (1), p.164

2005

Volltextzugriff (PDF)

The Function of Weeping in the Adult

Nursing forum (Hillsdale), 1980-01, Vol.19 (1), p.26-44

Lipe, Hillary P.

1980

Volltextzugriff (PDF)

Moving the Patient in Bed: Effects on Intracranial Pressure

Nursing research (New York), 1981-07, Vol.30 (4), p.212-218

1981

Volltextzugriff (PDF)

Bisphosphonates for delivering drugs to bone

British journal of pharmacology, 2021-05, Vol.178 (9), p.2008-2025

2021

Volltextzugriff (PDF)

Missense Mutations in the Regulatory Domain of PKCγ: A New Mechanism for Dominant Nonepisodic Cerebellar Ataxia

American journal of human genetics, 2003-04, Vol.72 (4), p.839-849

2003

Volltextzugriff (PDF)

Severe renal failure and thrombotic microangiopathy induced by malignant hypertension successfully treated with spironolactone

Annales de cardiologie et d'angeiologie, 2018-06, Vol.67 (3), p.208-214

2018

Volltextzugriff (PDF)

Thermoelectric transfer difference of thermal converters measured with a Josephson source

IEEE transactions on instrumentation and measurement, 1999-04, Vol.48 (2), p.282-284

1999

Volltextzugriff (PDF)

Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct genetic disorders

Neurology, 1994-12, Vol.44 (12), p.2253-2253

1994

Volltextzugriff (PDF)

1 – 25 von 34

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(29)
Mit Volltextzugriff
(21)

Publikationsform

Artikel
(33)
Tagungsberichte
(1)

Sprache

Englisch
(34)
Japanisch
(3)

Erscheinungsjahr

n.n

Thema

Humans
(25)
Science & Technology
(20)
Male
(19)
Life Sciences & Biomedicine
(17)
Adult
(16)
Biological And Medical Sciences
(16)
Female
(16)
Medical Sciences
(16)
Neurology
(14)
Clinical Neurology
(11)
Neurosciences & Neurology
(11)
Pedigree
(11)
Middle Aged
(10)
Child
(7)
Aged
(6)
Charcot-Marie-Tooth Disease - Genetics
(6)
Neurosciences
(5)
Nursing
(5)
Phenotype
(5)
Adolescent
(4)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C

The clinical and genetic spectrum of spinocerebellar ataxia 14

Late-onset hereditary axonal neuropathies

Charcot–Marie–Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genes

Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: A 20-year study

Familial spastic paraparesis: Evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2

Impotence associated with the Charcot-Marie-Tooth syndrome

Severe vincristine neuropathy in charcot‐marie‐tooth disease type 1A

Cerebral cavernous malformation: novel mutation in a Chinese family and evidence for heterogeneity

The use of apolipoprotein CII as a genetic marker for myotonic dystrophy

The Consequences of Testing for Huntington's Disease

Prevention of nervous system trauma from travel in motor vehicles

The neuro nurse specialist--present and future considerations

Positioning the patient with intracranial hypertension: how turning and head rotation affect the internal jugular vein

Double trouble in hereditary neuropathy: concomitant mutations in the PMP-22 gene and another gene produce novel phenotypes

Impact of presymptomatic genetic testing for hereditary ataxia and neuromuscular disorders

Severe vincristine neuropathy in Charcot-Marie-Tooth diseae type 1A

Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders: Where is the Evidence?—Reply

The Function of Weeping in the Adult

Moving the Patient in Bed: Effects on Intracranial Pressure

Bisphosphonates for delivering drugs to bone

Missense Mutations in the Regulatory Domain of PKCγ: A New Mechanism for Dominant Nonepisodic Cerebellar Ataxia

Severe renal failure and thrombotic microangiopathy induced by malignant hypertension successfully treated with spironolactone

Thermoelectric transfer difference of thermal converters measured with a Josephson source

Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct genetic disorders

Suchergebnisse filtern