UB Paderborn / Katalog / Suche / in CDI

Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia

Clinical genetics, 2017-01, Vol.91 (1), p.86-91

2017

Link zum Volltext

Verfügbarkeit prüfen

Neuroimaging Changes in Menkes Disease, Part 1

American journal of neuroradiology : AJNR, 2017-10, Vol.38 (10), p.1850-1857

2017

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

Neuroimaging Changes in Menkes Disease, Part 1

American journal of neuroradiology : AJNR, 2017-10, Vol.38 (10), p.1850-1857

2017

Link zum Volltext

Verfügbarkeit prüfen

Neuroimaging Changes in Menkes Disease, Part 2

American journal of neuroradiology : AJNR, 2017-10, Vol.38 (10), p.1858-1865

2017

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

Efficacy and tolerability of add-on lacosamide in children with Lennox-Gastaut syndrome

Acta neurologica Scandinavica, 2014-06, Vol.129 (6), p.420-424

2014

Link zum Volltext

Verfügbarkeit prüfen

Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication

European journal of neurology, 2016-02, Vol.23 (2), p.241-246

2016

Link zum Volltext

Verfügbarkeit prüfen

Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH)

Human molecular genetics, 1998-07, Vol.7 (7), p.1063-1070

1998

Link zum Volltext

Verfügbarkeit prüfen

Childhood refractory focal epilepsy following acute febrile encephalopathy

European journal of neurology, 2011-07, Vol.18 (7), p.952-961

2011

Link zum Volltext

Verfügbarkeit prüfen

Infantile ascending hereditary spastic paralysis (IAHSP): clinical features in 11 families

Neurology, 2003-02, Vol.60 (4), p.674

2003

Link zum Volltext

Verfügbarkeit prüfen

Mucositis pain: treatment pptions for the patient

Annals of oncology, 2016-09, Vol.27, p.iv103

2016

Link zum Volltext

Verfügbarkeit prüfen

Neuropsychiatric Aspects of Tuberous Sclerosis

Annals of the New York Academy of Sciences, 1991-04, Vol.615 (1), p.8-16

1991

Link zum Volltext

Verfügbarkeit prüfen

NEUROPSYCHOLOGICAL ASPECTS OF TUBEROUS SCLEROSIS IN RELATION TO EPILEPSY AND MRI FINDINGS

Developmental medicine and child neurology, 1991-08, Vol.33 (8), p.698-705

1991

Link zum Volltext

Verfügbarkeit prüfen

Convulsions associated with gastroenteritis in the spectrum of benign focal epilepsies in infancy: 30 cases including four cases with ictal EEG recording

Epileptic disorders, 2010-12, Vol.12 (4), p.255-261

2010

Link zum Volltext

Verfügbarkeit prüfen

Topographic Comparative Study of Magnetic Resonance Imaging and Electroencephalography in 34 Children with Tuberous Sclerosis

Epilepsia (Copenhagen), 1990-11, Vol.31 (6), p.747-755

1990

Link zum Volltext

Verfügbarkeit prüfen

PP6.2 – 1668 Early EEG monitoring following prenatal diagnosis predicts epileptogenesis in tuberous sclerosis

European journal of paediatric neurology, 2013-09, Vol.17, p.S45-S45

2013

Link zum Volltext

Verfügbarkeit prüfen

PS-033 Ifosfamide induced encephalopathy: prophylaxis and therapy with methylene blue

European journal of hospital pharmacy. Science and practice, 2017-03, Vol.24 (Suppl 1), p.A241-A243

2017

Link zum Volltext

Verfügbarkeit prüfen

P01.1 Epilepsy and cognitive long-term outcome is improved by prompt seizure control in children with tuberous sclerosis

European journal of paediatric neurology, 2011-05, Vol.15, p.S32-S32

2011

Link zum Volltext

Verfügbarkeit prüfen

The ketogenic diet in children, adolescents and young adults with refractory epilepsy: an Italian multicentric experience

Epilepsy research, 2002-02, Vol.48 (3), p.221-227

2002

Link zum Volltext

Verfügbarkeit prüfen

P63 – 1669 Rufinamide as adjunctive drug in refractory epilepsy due to neuronal migration disorders

European journal of paediatric neurology, 2013-09, Vol.17, p.S71-S71

2013

Link zum Volltext

Verfügbarkeit prüfen

P280 – 1775 Neurophysiological features in congenital disorders of glycosylation

European journal of paediatric neurology, 2013-09, Vol.17, p.S130-S130

2013

Link zum Volltext

Verfügbarkeit prüfen

CP-123 A cost effectiveness analysis of nivolumab compared with pemetrexed for the treatment of non-small cell lung cancer in real practice

European journal of hospital pharmacy. Science and practice, 2017-03, Vol.24 (Suppl 1), p.A55-A55

2017

Link zum Volltext

Verfügbarkeit prüfen

Childhood refractory focal epilepsy following acute febrile encephalopathy: Severe epilepsy after febrile encephalopathy

European journal of neurology, 2011-07, Vol.18 (7), p.952-961

2011

Link zum Volltext

Verfügbarkeit prüfen

Menü

Weitere Dienste

Einstellungen

Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia

Neuroimaging Changes in Menkes Disease, Part 1

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

Neuroimaging Changes in Menkes Disease, Part 1

Neuroimaging Changes in Menkes Disease, Part 2

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

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

Efficacy and tolerability of add-on lacosamide in children with Lennox-Gastaut syndrome

Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication

Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH)

Childhood refractory focal epilepsy following acute febrile encephalopathy

Infantile ascending hereditary spastic paralysis (IAHSP): clinical features in 11 families

Mucositis pain: treatment pptions for the patient

Neuropsychiatric Aspects of Tuberous Sclerosis

NEUROPSYCHOLOGICAL ASPECTS OF TUBEROUS SCLEROSIS IN RELATION TO EPILEPSY AND MRI FINDINGS

Convulsions associated with gastroenteritis in the spectrum of benign focal epilepsies in infancy: 30 cases including four cases with ictal EEG recording

Topographic Comparative Study of Magnetic Resonance Imaging and Electroencephalography in 34 Children with Tuberous Sclerosis

PP6.2 – 1668 Early EEG monitoring following prenatal diagnosis predicts epileptogenesis in tuberous sclerosis

PS-033 Ifosfamide induced encephalopathy: prophylaxis and therapy with methylene blue

P01.1 Epilepsy and cognitive long-term outcome is improved by prompt seizure control in children with tuberous sclerosis

The ketogenic diet in children, adolescents and young adults with refractory epilepsy: an Italian multicentric experience

P63 – 1669 Rufinamide as adjunctive drug in refractory epilepsy due to neuronal migration disorders

P280 – 1775 Neurophysiological features in congenital disorders of glycosylation

CP-123 A cost effectiveness analysis of nivolumab compared with pemetrexed for the treatment of non-small cell lung cancer in real practice

Childhood refractory focal epilepsy following acute febrile encephalopathy: Severe epilepsy after febrile encephalopathy

Suchergebnisse filtern