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...

Febrile infection–related epilepsy syndrome (FIRES): A nonencephalitic encephalopathy in childhood

Epilepsia (Copenhagen), 2010-07, Vol.51 (7), p.1323-1328

2010

Volltextzugriff (PDF)

Alternating Hemiplegia of Childhood as a New Presentation of Adenylate Cyclase 5 -Mutation-Associated Disease: A Report of Two Cases

The Journal of pediatrics, 2017-02, Vol.181, p.306-308.e1

2017

Volltextzugriff (PDF)

Microdeletion 5q14.3 and anomalies of brain development

American journal of medical genetics. Part A, 2013-09, Vol.161A (9), p.2124-2133

2013

Volltextzugriff (PDF)

New Syndrome Characterized by Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum

American journal of neuroradiology : AJNR, 2002-10, Vol.23 (9), p.1466-1474

2002

Volltextzugriff (PDF)

A De Novo Mutation in the β-Tubulin Gene TUBB4A Results in the Leukoencephalopathy Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum

American journal of human genetics, 2013-05, Vol.92 (5), p.767-773

2013

Volltextzugriff (PDF)

Operative and Technical Complications of Vagus Nerve Stimulator Implantation

Neurosurgery, 2010-12, Vol.67 (6), p.491-496

2010

Volltextzugriff (PDF)

Intracranial hypertension in neuroborreliosis

Developmental medicine and child neurology, 2002-09, Vol.44 (9), p.641-642

2002

Volltextzugriff (PDF)

Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region

Epilepsia (Copenhagen), 2010-09, Vol.51 (9), p.1870-1873

2010

Volltextzugriff (PDF)

Clinical and genetic features of myoclonus-dystonia in 3 cases: A video presentation

Movement disorders, 2004-02, Vol.19 (2), p.231-234

2004

Volltextzugriff (PDF)

Mutations in the X-Linked Cyclin-Dependent Kinase–Like 5 ( CDKL5/STK9) Gene Are Associated with Severe Neurodevelopmental Retardation

American journal of human genetics, 2004-12, Vol.75 (6), p.1149-1154

2004

Volltextzugriff (PDF)

Life-long increase of substantia nigra hyperechogenicity in transcranial sonography

NeuroImage (Orlando, Fla.), 2010-05, Vol.51 (1), p.28-32

2010

Volltextzugriff (PDF)

Right-sided vagus nerve stimulation in humans: An effective therapy?

Epilepsy research, 2008-12, Vol.82 (2), p.232-234

2008

Volltextzugriff (PDF)

Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?

Epilepsy research, 2015-08, Vol.114, p.47-51

2015

Volltextzugriff (PDF)

Evidence That Paternal Expression of the ε-Sarcoglycan Gene Accounts for Reduced Penetrance in Myoclonus-Dystonia

American journal of human genetics, 2002-12, Vol.71 (6), p.1303-1311

2002

Volltextzugriff (PDF)

Paroxysmal hemichorea after streptococcal infection-clinical and diagnostic findings

Journal of pediatric neurology, 2015-07, Vol.1 (2), p.103-106

2015

Volltextzugriff (PDF)

Cerebral hemiatrophy associated with hippocampal sclerosis following a single prolonged febrile seizure

European journal of pediatrics, 2011-06, Vol.170 (6), p.789-794

2011

Volltextzugriff (PDF)

A De Novo Mutation in the [Beta]-Tubulin Gene TUBB4A Results in the Leukoencephalopathy Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum

American journal of human genetics, 2013-05, Vol.92 (5), p.767

2013

Volltextzugriff (PDF)

Lyme disease with lymphocytic meningitis, trigeminal palsy and silent thalamic lesion

European journal of paediatric neurology, 2008-11, Vol.12 (6), p.501-504

2008

Volltextzugriff (PDF)

Cerebral proton magnetic resonance spectroscopy in infantile Alexander disease

Journal of neurology, 2003-03, Vol.250 (3), p.300-306

2003

Volltextzugriff (PDF)

Cerebrovascular Reactivity in Adolescents With Migraine and Tension-Type Headache During Headache-Free Interval and Attack

Headache, 2003-05, Vol.43 (5), p.458-463

2003

Volltextzugriff (PDF)

Epilepsia partialis continua associated with a homoplasmic mitochondrial tRNA(Ser(UCN)) mutation

Annals of neurology, 1998-10, Vol.44 (4), p.700-704

1998

Volltextzugriff (PDF)

Beneficial prenatal levodopa therapy in autosomal recessive guanosine triphosphate cyclohydrolase 1 deficiency

Archives of neurology (Chicago), 2012-08, Vol.69 (8), p.1071

2012

Volltextzugriff (PDF)

Frontoethmoidal encephalocele with ocular leakage of cerebrospinal fluid. Case report

Journal of neurosurgery, 2004-11, Vol.101 (2 Suppl), p.218-221

2004

Volltextzugriff (PDF)

Intracranial hypertension in neuroborreliosis

Developmental medicine and child neurology, 2002-09, Vol.44 (9), p.641-642

2002

Volltextzugriff (PDF)

Isolated unilateral cortical oedema and complex partial seizures in association with coxsackievirus B infection

Epilepsy & behavior, 2002-10, Vol.3 (5), p.480-482

2002

Volltextzugriff (PDF)

1 – 25 von 44

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(35)
Mit Volltextzugriff
(36)

Publikationsform

Sprache

Englisch
(39)
Deutsch
(5)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Febrile infection–related epilepsy syndrome (FIRES): A nonencephalitic encephalopathy in childhood

Alternating Hemiplegia of Childhood as a New Presentation of Adenylate Cyclase 5 -Mutation-Associated Disease: A Report of Two Cases

Microdeletion 5q14.3 and anomalies of brain development

New Syndrome Characterized by Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum

A De Novo Mutation in the β-Tubulin Gene TUBB4A Results in the Leukoencephalopathy Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum

Operative and Technical Complications of Vagus Nerve Stimulator Implantation

Intracranial hypertension in neuroborreliosis

Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region

Clinical and genetic features of myoclonus-dystonia in 3 cases: A video presentation

Mutations in the X-Linked Cyclin-Dependent Kinase–Like 5 ( CDKL5/STK9) Gene Are Associated with Severe Neurodevelopmental Retardation

Life-long increase of substantia nigra hyperechogenicity in transcranial sonography

Right-sided vagus nerve stimulation in humans: An effective therapy?

Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?

Evidence That Paternal Expression of the ε-Sarcoglycan Gene Accounts for Reduced Penetrance in Myoclonus-Dystonia

Paroxysmal hemichorea after streptococcal infection-clinical and diagnostic findings

Cerebral hemiatrophy associated with hippocampal sclerosis following a single prolonged febrile seizure

A De Novo Mutation in the [Beta]-Tubulin Gene TUBB4A Results in the Leukoencephalopathy Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum

Lyme disease with lymphocytic meningitis, trigeminal palsy and silent thalamic lesion

Cerebral proton magnetic resonance spectroscopy in infantile Alexander disease

Cerebrovascular Reactivity in Adolescents With Migraine and Tension-Type Headache During Headache-Free Interval and Attack

Epilepsia partialis continua associated with a homoplasmic mitochondrial tRNA(Ser(UCN)) mutation

Beneficial prenatal levodopa therapy in autosomal recessive guanosine triphosphate cyclohydrolase 1 deficiency

Frontoethmoidal encephalocele with ocular leakage of cerebrospinal fluid. Case report

Intracranial hypertension in neuroborreliosis

Isolated unilateral cortical oedema and complex partial seizures in association with coxsackievirus B infection

Suchergebnisse filtern