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A systematic review of magnetic resonance imaging in patients with an implanted vagus nerve stimulation system

Neuroradiology, 2021-09, Vol.63 (9), p.1407-1417

2021

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Pharmacologic stabilization of hypoxia-inducible transcription factors protects developing mouse brain from hypoxia-induced apoptotic cell death

Neuroscience, 2014-10, Vol.278, p.327-342

2014

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Diagnosis and treatment of Guillain-Barré Syndrome in childhood and adolescence: An evidence- and consensus-based guideline

European journal of paediatric neurology, 2020-03, Vol.25, p.5-16

2020

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Predicting multiple sclerosis following isolated optic neuritis in children

European journal of neurology, 2013-09, Vol.20 (9), p.1292-1296

2013

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Rare intronic mutation between Exon 62 and 63 (c.9225–285A>G) of the dystrophin gene associated with atypical BMD phenotype

Neuromuscular disorders : NMD, 2020-08, Vol.30 (8), p.680-684

2020

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Hypoxia-inducible transcription factors (HIF)-dependent growth factors protect the developing mouse brain against acute hypoxic injury

European journal of paediatric neurology, 2017-06, Vol.21, p.e12-e12

2017

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Treatment of severe traumatic brain injury in German pediatric intensive care units—a survey of current practice

Child's nervous system, 2019-05, Vol.35 (5), p.815-822

2019

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Autoimmunenzephalopathien bei Kindern: Diagnostik und Therapie

Monatsschrift Kinderheilkunde, 2015-06, Vol.163 (6), p.560-569

Trollmann, R.

2015

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Cardiomyopathy in Duchenne Muscular Dystrophy: Current Value of Clinical, Electrophysiological and Imaging Findings in Children and Teenagers

Klinische Padiatrie, 2015-07, Vol.227 (4), p.225-231

2015

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Transition bei neuromuskulären Erkrankungen mit chronisch respiratorischer Insuffizienz

Pneumologe, 2021-03, Vol.18 (2), p.116-122

2021

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1089 Visual Evoked Potentials in Term and Preterm Infants

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A312-A312

2012

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On the interdisciplinary S3 guidelines for the treatment of chronic idiopathic tinnitus

HNO, 2015-06, Vol.63 (6), p.419-427

2015

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Editorial

Frauenheilkunde up2date, 2012-12, Vol.6 (6), p.345-346

Trollmann, R.

2012

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Hypoxia activates the human placental vascular endothelial growth factor system in vitro and in vivo: Up-regulation of vascular endothelial growth factor in clinically relevant hypoxic ischemia in birth asphyxia

American journal of obstetrics and gynecology, 2003-02, Vol.188 (2), p.517-523

2003

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PP03.1 – 3059: Mutations in ECHS1: A defect in a multifunctional enzyme causing a mitochondrial disorder

European journal of paediatric neurology, 2015-05, Vol.19, p.S36-S36

2015

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P106 Impact of a computerised physician order entry system on medication safety in paediatrics

Archives of disease in childhood, 2019-06, Vol.104 (6), p.e62-e62

2019

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O01 Drug-related hospital admissions in paediatrics – what is preventable?

Archives of disease in childhood, 2019-06, Vol.104 (6), p.e1-e1

2019

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OP64 – 2760: Oligoclonal bands predict multiple sclerosis in children with isolated optic neuritis

European journal of paediatric neurology, 2015-05, Vol.19, p.S20-S21

2015

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The effect of valproate therapy on thrombin generation determined by calibrated automated thrombography

Klinische Padiatrie, 2011-05, Vol.223 (3), p.165

2011

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Papilledema and echographically detectable retro-orbital dilatation of the sub-arachnoidal space with open fontanelle - six case reports

Klinische Monatsblatter fur Augenheilkunde, 2011-11, Vol.228 (11), p.963

2011

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Histopathological Proof of the Pathogenetic Role of a Rare GFAP Mutation in Alexander´s Disease with Isolated Flaccid Paraparesis

Neuropediatrics, 2017, Vol.48 (S 01), p.S1-S45

2017

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BNS Epilepsy, Global Developmental Delay, Optic Coloboma, and Vesicoureteral Reflux as Leading Symptoms of COL4A1 Mutation: A Case Report

Neuropediatrics, 2017, Vol.48 (S 01), p.S1-S45

2017

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Toxic Rapidly Progressive Myelopathy Induced by Nelarabine in an Adolescent with Relapsed Pre-T-ALL

Neuropediatrics, 2017, Vol.48 (S 01), p.S1-S45

2017

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Compound heterozygous RYR1 mutations in a preterm with arthrogryposis multiplex congenita and prenatal CNS bleeding

Neuromuscular disorders : NMD, 2018-01, Vol.28 (1), p.54-58

2018

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Isolated optic neuritis is associated with development of pediatric multiple sclerosis

Neuropediatrics, 2011, Vol.42 (S 01)

2011

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A systematic review of magnetic resonance imaging in patients with an implanted vagus nerve stimulation system

Pharmacologic stabilization of hypoxia-inducible transcription factors protects developing mouse brain from hypoxia-induced apoptotic cell death

Diagnosis and treatment of Guillain-Barré Syndrome in childhood and adolescence: An evidence- and consensus-based guideline

Predicting multiple sclerosis following isolated optic neuritis in children

Rare intronic mutation between Exon 62 and 63 (c.9225–285A>G) of the dystrophin gene associated with atypical BMD phenotype

Hypoxia-inducible transcription factors (HIF)-dependent growth factors protect the developing mouse brain against acute hypoxic injury

Treatment of severe traumatic brain injury in German pediatric intensive care units—a survey of current practice

Autoimmunenzephalopathien bei Kindern: Diagnostik und Therapie

Cardiomyopathy in Duchenne Muscular Dystrophy: Current Value of Clinical, Electrophysiological and Imaging Findings in Children and Teenagers

Transition bei neuromuskulären Erkrankungen mit chronisch respiratorischer Insuffizienz

1089 Visual Evoked Potentials in Term and Preterm Infants

On the interdisciplinary S3 guidelines for the treatment of chronic idiopathic tinnitus

Editorial

Hypoxia activates the human placental vascular endothelial growth factor system in vitro and in vivo: Up-regulation of vascular endothelial growth factor in clinically relevant hypoxic ischemia in birth asphyxia

PP03.1 – 3059: Mutations in ECHS1: A defect in a multifunctional enzyme causing a mitochondrial disorder

P106 Impact of a computerised physician order entry system on medication safety in paediatrics

O01 Drug-related hospital admissions in paediatrics – what is preventable?

OP64 – 2760: Oligoclonal bands predict multiple sclerosis in children with isolated optic neuritis

The effect of valproate therapy on thrombin generation determined by calibrated automated thrombography

Papilledema and echographically detectable retro-orbital dilatation of the sub-arachnoidal space with open fontanelle - six case reports

Histopathological Proof of the Pathogenetic Role of a Rare GFAP Mutation in Alexander´s Disease with Isolated Flaccid Paraparesis

BNS Epilepsy, Global Developmental Delay, Optic Coloboma, and Vesicoureteral Reflux as Leading Symptoms of COL4A1 Mutation: A Case Report

Toxic Rapidly Progressive Myelopathy Induced by Nelarabine in an Adolescent with Relapsed Pre-T-ALL

Compound heterozygous RYR1 mutations in a preterm with arthrogryposis multiplex congenita and prenatal CNS bleeding

Isolated optic neuritis is associated with development of pediatric multiple sclerosis

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