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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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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

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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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Severe congenital myopathy with myasthenic features and lethal neurodegeneration – A new ALG14-related phenotype?

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S112-S112

2016

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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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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

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Obesity after childhood craniopharyngioma - German multicenter study on pre-operative risk factors and quality of life

Klinische Pädiatrie, 2001-07, Vol.213 (4), p.244-249

2001

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Teaching Neuroimages: Basal Ganglia Germinoma with Hemiatrophy

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

2016

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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

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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

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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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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

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Clinical and Experimental Results on Cardiac Troponin Expression in Duchenne Muscular Dystrophy

Clinical chemistry (Baltimore, Md.), 2001-03, Vol.47 (3), p.451-458

2001

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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

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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

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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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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

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Natural history and treatment effects in Guillain-Barré syndrome: a multicentre study

Archives of disease in childhood, 1996-04, Vol.74 (4), p.281-287

1996

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The Heart in Friedreich Ataxia: Definition of Cardiomyopathy, Disease Severity, and Correlation With Neurological Symptoms

Circulation (New York, N.Y.), 2012-04, Vol.125 (13), p.1626-1634

2012

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Identification of seven novel mutations in the GAN gene

Human mutation, 2003-04, Vol.21 (4), p.446-446

2003

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P3.52 FOR-DMD: double-blind randomized trial to optimize steroid regime in Duchenne Muscular Dystrophy (DMD)

Neuromuscular disorders : NMD, 2010-10, Vol.20 (9), p.657-657

2010

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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

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

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

Severe congenital myopathy with myasthenic features and lethal neurodegeneration – A new ALG14-related phenotype?

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

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

Obesity after childhood craniopharyngioma - German multicenter study on pre-operative risk factors and quality of life

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

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

Clinical and Experimental Results on Cardiac Troponin Expression in Duchenne Muscular Dystrophy

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

Predicting respiratory failure and outcome in pediatric Guillain-Barré syndrome

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

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

Natural history and treatment effects in Guillain-Barré syndrome: a multicentre study

The Heart in Friedreich Ataxia: Definition of Cardiomyopathy, Disease Severity, and Correlation With Neurological Symptoms

Identification of seven novel mutations in the GAN gene

P3.52 FOR-DMD: double-blind randomized trial to optimize steroid regime in Duchenne Muscular Dystrophy (DMD)

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