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...

Posterior reversible encephalopathy syndrome: The endothelial hypotheses

Medical hypotheses, 2014-05, Vol.82 (5), p.619-622

2014

Volltextzugriff (PDF)

Lamotrigine induced Brugada-pattern in a patient with genetic epilepsy associated with a novel variant in SCN9A

Gene, 2020-09, Vol.754, p.144847-144847, Article 144847

2020

Volltextzugriff (PDF)

Electroclinical features of epilepsy associated with 1p36 deletion syndrome: A review

Epilepsy research, 2018-01, Vol.139, p.92-101

2018

Volltextzugriff (PDF)

Rasmussen's encephalitis: From immune pathogenesis towards targeted-therapy

Seizure (London, England), 2020-10, Vol.81, p.76-83

2020

Volltextzugriff (PDF)

Neuroimaging Features of Biotinidase Deficiency

American journal of neuroradiology : AJNR, 2023-03, Vol.44 (3), p.328-333

2023

Volltextzugriff (PDF)

An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy

Neurology, 2007-07, Vol.69 (3), p.250-254

2007

Volltextzugriff (PDF)

Post-traumatic stress, anxiety, and depressive symptoms in caregivers of children tested for COVID-19 in the acute phase of the Italian outbreak

Journal of psychiatric research, 2021-03, Vol.135, p.256-263

2021

Volltextzugriff (PDF)

Neuroinflammation and status epilepticus: a narrative review unraveling a complex interplay

Frontiers in pediatrics, 2023-11, Vol.11, p.1251914-1251914

2023

Volltextzugriff (PDF)

Effectiveness and tolerability of Perampanel in children and adolescents with refractory epilepsies − an Italian observational multicenter study

Epilepsy research, 2016-11, Vol.127, p.93-100

2016

Volltextzugriff (PDF)

Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype

Acta neurologica Scandinavica, 2005-04, Vol.111 (4), p.211-217

2005

Volltextzugriff (PDF)

Clinical and genetic spectrum of SCN2A-associated episodic ataxia

European journal of paediatric neurology, 2019-05, Vol.23 (3), p.438-447

2019

Volltextzugriff (PDF)

Reply to 'Hitting two birds with one stone: daily scheduled opiods in preventing migraine and migraine-related epilepsy (migralepsy)'

European journal of neurology, 2016-09, Vol.23 (9), p.e60-e61

2016

Volltextzugriff (PDF)

Histopathologic features of selumetinib‐induced paronychia in a child with neurofibromatosis type 1

JEADV clinical practice, 2024-06, Vol.3 (2), p.664-667

2024

Volltextzugriff (PDF)

Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation

Neurology, 2011-03, Vol.76 (13), p.1173-1176

2011

Volltextzugriff (PDF)

Electroclinical findings and long‐term outcomes in epileptic patients with inv dup (15)

Acta neurologica Scandinavica, 2018-06, Vol.137 (6), p.575-581

2018

Volltextzugriff (PDF)

Phenotypic variability in xeroderma pigmentosum group G: An uncommon case with severe prenatal‐onset Cockayne syndrome features

Clinical genetics, 2018-10, Vol.94 (3-4), p.386-388

2018

Volltextzugriff (PDF)

Interictal and periictal headache in patients with epilepsy: migraine-triggered seizures or epilepsy-triggered headache?

European journal of neurology, 2013-10, Vol.20 (10), p.1333-1334

2013

Volltextzugriff (PDF)

Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations

Brain (London, England : 1878), 2006-07, Vol.129 (7), p.1892-1906

2006

Volltextzugriff (PDF)

GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy

Neurology, 2012-02, Vol.78 (8), p.557-562

2012

Volltextzugriff (PDF)

De novo Absence Status Epilepticus in a pediatric cohort: Electroclinical pattern in a multicenter Italian patients cohort

Seizure (London, England), 2019-12, Vol.73, p.79-82

2019

Volltextzugriff (PDF)

A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures

Neurology, 2007-06, Vol.68 (24), p.2150-2151

2007

Volltextzugriff (PDF)

LGI1 microdeletion in autosomal dominant lateral temporal epilepsy

Neurology, 2012-04, Vol.78 (17), p.1299-1303

2012

Volltextzugriff (PDF)

Generalized epilepsy and mild intellectual disability associated with 13q34 deletion: A potential role for SOX1 and ARHGEF7

Seizure (London, England), 2018-07, Vol.59, p.38-40

2018

Volltextzugriff (PDF)

A validation study of the clinical diagnosis of Dup15q syndrome: Which symptoms matter most?

Seizure (London, England), 2020-01, Vol.74, p.26-30

2020

Volltextzugriff (PDF)

Retrospective evaluation of low long-term efficacy of antiepileptic drugs and ketogenic diet in 39 patients with CDKL5 -related epilepsy

European journal of paediatric neurology, 2016-01, Vol.20 (1), p.147-151

2016

Volltextzugriff (PDF)

1 – 25 von 264

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(242)
Mit Volltextzugriff
(224)

Publikationsform

Sprache

Englisch
(260)
Italienisch
(4)

Erscheinungsjahr

n.n

Thema

Science & Technology
(203)
Life Sciences & Biomedicine
(192)
Humans
(171)
Neurosciences & Neurology
(135)
Clinical Neurology
(128)
Female
(113)
Male
(111)
Epilepsy
(93)
Adult
(82)
Neurology
(71)
Biological And Medical Sciences
(60)
Medical Sciences
(53)
Neurosciences
(53)
Child
(49)
Adolescent
(46)
Middle Aged
(43)
Nervous System
(34)
Electroencephalography
(33)
Anticonvulsants - Therapeutic Use
(32)
Headache. Facial Pains. Syncopes. Epilepsia. Intracranial Hypertension. Brain Oedema. Cerebral Palsy
(32)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Epilepsia
(31)
Brain
(14)
Seizure
(10)
Neurology
(9)
American Journal Of Human Genetics
(8)
Epilepsy Research
(8)
Acta Neurologica Scandinavica
(6)
European Journal Of Paediatric Neurology
(6)
Movement Disorders
(6)
European Journal Of Neurology
(5)

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Posterior reversible encephalopathy syndrome: The endothelial hypotheses

Lamotrigine induced Brugada-pattern in a patient with genetic epilepsy associated with a novel variant in SCN9A

Electroclinical features of epilepsy associated with 1p36 deletion syndrome: A review

Rasmussen's encephalitis: From immune pathogenesis towards targeted-therapy

Neuroimaging Features of Biotinidase Deficiency

An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy

Post-traumatic stress, anxiety, and depressive symptoms in caregivers of children tested for COVID-19 in the acute phase of the Italian outbreak

Neuroinflammation and status epilepticus: a narrative review unraveling a complex interplay

Effectiveness and tolerability of Perampanel in children and adolescents with refractory epilepsies − an Italian observational multicenter study

Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype

Clinical and genetic spectrum of SCN2A-associated episodic ataxia

Reply to 'Hitting two birds with one stone: daily scheduled opiods in preventing migraine and migraine-related epilepsy (migralepsy)'

Histopathologic features of selumetinib‐induced paronychia in a child with neurofibromatosis type 1

Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation

Electroclinical findings and long‐term outcomes in epileptic patients with inv dup (15)

Phenotypic variability in xeroderma pigmentosum group G: An uncommon case with severe prenatal‐onset Cockayne syndrome features

Interictal and periictal headache in patients with epilepsy: migraine-triggered seizures or epilepsy-triggered headache?

Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations

GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy

De novo Absence Status Epilepticus in a pediatric cohort: Electroclinical pattern in a multicenter Italian patients cohort

A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures

LGI1 microdeletion in autosomal dominant lateral temporal epilepsy

Generalized epilepsy and mild intellectual disability associated with 13q34 deletion: A potential role for SOX1 and ARHGEF7

A validation study of the clinical diagnosis of Dup15q syndrome: Which symptoms matter most?

Retrospective evaluation of low long-term efficacy of antiepileptic drugs and ketogenic diet in 39 patients with CDKL5 -related epilepsy

Suchergebnisse filtern