UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 277

Sortiert nach

Joseph Roger. 1918–2012

Neurophysiologie clinique, 2014-04, Vol.44 (2), p.151-152

2014

Volltextzugriff (PDF)

Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome

Journal of medical genetics, 2010-06, Vol.47 (6), p.404-410

2010

Volltextzugriff (PDF)

Do carbamazepine and phenytoin aggravate juvenile myoclonic epilepsy?

Neurology, 2000-10, Vol.55 (8), p.1106

2000

Volltextzugriff (PDF)

Joseph Roger. 1918-2012

Neurophysiologie clinique, 2014-04, Vol.44 (2), p.151-152

2014

Volltextzugriff (PDF)

How Dravet syndrome became a model for studying childhood genetic epilepsies

Brain (London, England : 1878), 2012-08, Vol.135 (Pt 8), p.2309-2311

Dravet, Charlotte

2012

Volltextzugriff (PDF)

Clinical factors of drug resistance in juvenile myoclonic epilepsy

Journal of neurology, neurosurgery and psychiatry, 2001-02, Vol.70 (2), p.240-243

2001

Volltextzugriff (PDF)

Somatosensory mismatch negativity in Dravet Syndrome

European journal of paediatric neurology, 2017-06, Vol.21, p.e143-e144

2017

Volltextzugriff (PDF)

Multilobar polymicrogyria, intractable drop attack seizures, and sleep-related electrical status epilepticus

Neurology, 1998-08, Vol.51 (2), p.504

1998

Volltextzugriff (PDF)

Radiosurgery for trigeminal neuralgia and epilepsy

Neurosurgery clinics of North America, 1999-04, Vol.10 (2), p.359

1999

Volltextzugriff (PDF)

Absence Epilepsy with Fast Rhythmic Discharges During Sleep: An Intermediary Form of Generalized Epilepsy?

Epilepsia (Copenhagen), 2001-03, Vol.42 (3), p.351-356

2001

Volltextzugriff (PDF)

Early Thalamic Injury Associated with Epilepsy and Continuous Spike–Wave during Slow Sleep

Epilepsia (Copenhagen), 2005-06, Vol.46 (6), p.889-900

2005

Volltextzugriff (PDF)

Lamotrigine and Seizure Aggravation in Severe Myoclonic Epilepsy

Epilepsia (Copenhagen), 1998-05, Vol.39 (5), p.508-512

1998

Volltextzugriff (PDF)

Apport de l'enregistrement EEG ambulatoire (Medilog 9000) dans une population d'epileptiques

Neurophysiologie clinique, 1989, Vol.19 (3), p.219-230

1989

Volltextzugriff (PDF)

Epileptic negative myoclonus

Neurology, 1993-06, Vol.43 (6), p.1078

1993

Volltextzugriff (PDF)

Etude de l'EEG de sieste dans les epilepsies partielles idiopathiques et symptomatiques de l'enfant

Neurophysiologie clinique, 1988-08, Vol.18 (4), p.333-343

1988

Volltextzugriff (PDF)

Cost Minimization Analysis of Antiepileptic Drugs in Newly Diagnosed Epilepsy in 12 European Countries

Epilepsia (Copenhagen), 2000-01, Vol.41 (S5), p.S37-S44

2000

Volltextzugriff (PDF)

Particularites electro-encephalographiques des epilepsies partielles symptomatiques severes de l'enfant

Neurophysiologie clinique, 1989, Vol.19 (3), p.209-218

1989

Volltextzugriff (PDF)

In memoriam, Henri Gastaut, 1915-1995

Epilepsia (Copenhagen), 1996-04, Vol.37 (4), p.410-415

1996

Volltextzugriff (PDF)

Partial Epilepsies in Infancy: A Study of 40 Cases

Epilepsia (Copenhagen), 1989-11, Vol.30 (6), p.807-812

1989

Volltextzugriff (PDF)

Abnormal Neuroimaging in Patients with Benign Epilepsy with Centrotemporal Spikes

Epilepsia (Copenhagen), 2003-03, Vol.44 (3), p.372-378

2003

Volltextzugriff (PDF)

Epilepsy, antiepileptic drugs, and malformations in children of women with epilepsy: a French prospective cohort study

Neurology, 1992-04, Vol.42 (4 Suppl 5), p.75

1992

Volltextzugriff (PDF)

P28 – 2016 Cognitive and behavioural study of 24 consecutive patients with a Dravet syndrome

European journal of paediatric neurology, 2013-09, Vol.17, p.S61-S62

2013

Volltextzugriff (PDF)

Epilepsie myoclonique sévère, épilepsie myoclonique bénigne, épilepsie myoclono-astatique (DOOSE) : étude neuropsychologique (Résultats préliminaires)

Epilepsies, 1997, Vol.9 (3-4), p.191-194

1997

Volltextzugriff (PDF)

Incidence of Drug‐Induced Aggravation in Benign Epilepsy with Centrotemporal Spikes

Epilepsia (Copenhagen), 2001-06, Vol.42 (6), p.754-759

2001

Volltextzugriff (PDF)

Gamma Knife Surgery for Mesial Temporal Lobe Epilepsy

Epilepsia (Copenhagen), 1999-11, Vol.40 (11), p.1551-1556

1999

Volltextzugriff (PDF)

1 – 25 von 277

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(191)
Mit Volltextzugriff
(188)

Publikationsform

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Joseph Roger. 1918–2012

Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome

Do carbamazepine and phenytoin aggravate juvenile myoclonic epilepsy?

Joseph Roger. 1918-2012

How Dravet syndrome became a model for studying childhood genetic epilepsies

Clinical factors of drug resistance in juvenile myoclonic epilepsy

Somatosensory mismatch negativity in Dravet Syndrome

Multilobar polymicrogyria, intractable drop attack seizures, and sleep-related electrical status epilepticus

Radiosurgery for trigeminal neuralgia and epilepsy

Absence Epilepsy with Fast Rhythmic Discharges During Sleep: An Intermediary Form of Generalized Epilepsy?

Early Thalamic Injury Associated with Epilepsy and Continuous Spike–Wave during Slow Sleep

Lamotrigine and Seizure Aggravation in Severe Myoclonic Epilepsy

Apport de l'enregistrement EEG ambulatoire (Medilog 9000) dans une population d'epileptiques

Epileptic negative myoclonus

Etude de l'EEG de sieste dans les epilepsies partielles idiopathiques et symptomatiques de l'enfant

Cost Minimization Analysis of Antiepileptic Drugs in Newly Diagnosed Epilepsy in 12 European Countries

Particularites electro-encephalographiques des epilepsies partielles symptomatiques severes de l'enfant

In memoriam, Henri Gastaut, 1915-1995

Partial Epilepsies in Infancy: A Study of 40 Cases

Abnormal Neuroimaging in Patients with Benign Epilepsy with Centrotemporal Spikes

Epilepsy, antiepileptic drugs, and malformations in children of women with epilepsy: a French prospective cohort study

P28 – 2016 Cognitive and behavioural study of 24 consecutive patients with a Dravet syndrome

Epilepsie myoclonique sévère, épilepsie myoclonique bénigne, épilepsie myoclono-astatique (DOOSE) : étude neuropsychologique (Résultats préliminaires)

Incidence of Drug‐Induced Aggravation in Benign Epilepsy with Centrotemporal Spikes

Gamma Knife Surgery for Mesial Temporal Lobe Epilepsy

Suchergebnisse filtern