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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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A new era in the management of Duchenne muscular dystrophy

Developmental medicine and child neurology, 2019-03, Vol.61 (3), p.292-297

Korinthenberg, Rudolf

2019

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Mitochondrial DNA mutation 14487T>C manifesting as Leber’s hereditary optic neuropathy

Journal of neurology, 2015-12, Vol.262 (12), p.2776-2779

2015

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A further case with chronic hemolysis, CIDP and lethal cerebral vasculitis due to a CD59 mutation

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S143-S143

2016

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German registry of paediatric deep brain stimulation in patients with childhood-onset dystonia (GEPESTIM)

European journal of paediatric neurology, 2017-01, Vol.21 (1), p.136-146

2017

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T.I.3 The rationale for immunosuppressive treatment in DMD

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.830-830

Korinthenberg, R

2008

Volltextzugriff (PDF)

Hammersmith Functional Motor Scale and Motor Function Measure-20 in non ambulant SMA patients

Neuromuscular disorders : NMD, 2014-04, Vol.24 (4), p.347-352

2014

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Handlungsempfehlung nach der Leitlinie „Guillain-Barré Syndrom im Kindes- und Jugendalter

Monatsschrift Kinderheilkunde, 2013-12, Vol.161 (12), p.1201-1202

Korinthenberg, R.

2013

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Six minute walk test in type III spinal muscular atrophy: A 12 month longitudinal study

Neuromuscular disorders : NMD, 2013-08, Vol.23 (8), p.624-628

2013

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Echocardiographic and electrocardiographic findings of cardiomyopathy in Duchenne and Becker-Kiener muscular dystrophies

Pediatric cardiology, 2005-02, Vol.26 (1), p.66-72

2005

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Somatropin treatment of spinal muscular atrophy: A placebo-controlled, double-blind crossover pilot study

Neuromuscular disorders : NMD, 2014-02, Vol.24 (2), p.134-142

2014

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Six minute walk test in type III spinal muscular atrophy: A 12month longitudinal study

Neuromuscular disorders : NMD, 2013-08, Vol.23 (8), p.624-628

2013

Volltextzugriff (PDF)

Teaching Neuroimages: Basal Ganglia Germinoma with Hemiatrophy

Clinical neuroradiology (Munich), 2016-03, Vol.26 (1), p.97-98

2016

Volltextzugriff (PDF)

The TREAT-NMD Advisory Committee for Therapeutics (TACT): An innovative de-risking model to foster orphan drug development

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S271-S271

2015

Volltextzugriff (PDF)

Incidence of vasculopathy in children with hypothalamic/chiasmatic gliomas treated with brachytherapy

Child's nervous system, 2011-06, Vol.27 (6), p.961-966

2011

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Musculoskeletal pain: a new algorithm for differential diagnosis of a cardinal symptom in pediatrics

Klinische Padiatrie, 2014-04, Vol.226 (2), p.86

2014

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Prospective study on anti-ganglioside antibodies in childhood Guillain–Barré syndrome

Archives of disease in childhood, 2007-01, Vol.92 (1), p.48-52

2007

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

P.188 - A further case with chronic hemolysis, CIDP and lethal cerebral vasculitis due to a CD59 mutation

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S143-S143

2016

Volltextzugriff (PDF)

Peripheral neuropathy as the sole initial finding in three children with infantile metachromatic leukodystrophy

European journal of paediatric neurology, 2009-05, Vol.13 (3), p.257-260

2009

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G.P.2 Mutations in the human isoprenoid synthase domain containing gene are a common cause of congenital and limb girdle muscular dystrophies

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.812-812

2012

Volltextzugriff (PDF)

G.P.3.09 Mutation in PDHA1 gene mimicking a Guillain-Barré-Syndrome

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.754-754

2008

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Predicting respiratory failure and outcome in pediatric Guillain-Barré syndrome

European journal of paediatric neurology, 2023-05, Vol.44, p.18-24

2023

Volltextzugriff (PDF)

M.P.1.09 TREAT-NMD Clinical Trials Coordination Centre: Efficiency of networking

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.548-549

2009

Volltextzugriff (PDF)

Autoimmune Encephalitis with Autoantibodies to NMDAR1 following Herpes Encephalitis in Children and Adolescents

Neuropediatrics, 2023-02, Vol.54 (1), p.14

2023

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

A new era in the management of Duchenne muscular dystrophy

Mitochondrial DNA mutation 14487T>C manifesting as Leber’s hereditary optic neuropathy

A further case with chronic hemolysis, CIDP and lethal cerebral vasculitis due to a CD59 mutation

German registry of paediatric deep brain stimulation in patients with childhood-onset dystonia (GEPESTIM)

T.I.3 The rationale for immunosuppressive treatment in DMD

Hammersmith Functional Motor Scale and Motor Function Measure-20 in non ambulant SMA patients

Handlungsempfehlung nach der Leitlinie „Guillain-Barré Syndrom im Kindes- und Jugendalter

Six minute walk test in type III spinal muscular atrophy: A 12 month longitudinal study

Echocardiographic and electrocardiographic findings of cardiomyopathy in Duchenne and Becker-Kiener muscular dystrophies

Somatropin treatment of spinal muscular atrophy: A placebo-controlled, double-blind crossover pilot study

Six minute walk test in type III spinal muscular atrophy: A 12month longitudinal study

Teaching Neuroimages: Basal Ganglia Germinoma with Hemiatrophy

The TREAT-NMD Advisory Committee for Therapeutics (TACT): An innovative de-risking model to foster orphan drug development

Incidence of vasculopathy in children with hypothalamic/chiasmatic gliomas treated with brachytherapy

Musculoskeletal pain: a new algorithm for differential diagnosis of a cardinal symptom in pediatrics

Prospective study on anti-ganglioside antibodies in childhood Guillain–Barré syndrome

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

P.188 - A further case with chronic hemolysis, CIDP and lethal cerebral vasculitis due to a CD59 mutation

Peripheral neuropathy as the sole initial finding in three children with infantile metachromatic leukodystrophy

G.P.2 Mutations in the human isoprenoid synthase domain containing gene are a common cause of congenital and limb girdle muscular dystrophies

G.P.3.09 Mutation in PDHA1 gene mimicking a Guillain-Barré-Syndrome

Predicting respiratory failure and outcome in pediatric Guillain-Barré syndrome

M.P.1.09 TREAT-NMD Clinical Trials Coordination Centre: Efficiency of networking

Autoimmune Encephalitis with Autoantibodies to NMDAR1 following Herpes Encephalitis in Children and Adolescents

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