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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 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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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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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

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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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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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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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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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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

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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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Compound heterozygosity of the protein S-gene as a cause of severe cerebral sinovenous thrombosis in a 7-year-old child

Klinische Padiatrie, 2010-05, Vol.222 (3), p.194

2010

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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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Aicardi-Goutières-Syndrom: Seltene genetische Erkrankung imitiert intrauterine Virusinfektion

Monatsschrift Kinderheilkunde, 2009-05, Vol.157 (5), p.473-478

2009

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Peripheral Nerve Demyelination Caused by a Mutant Rho GTPase Guanine Nucleotide Exchange Factor, Frabin/FGD4

American journal of human genetics, 2007-07, Vol.81 (1), p.158-164

2007

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T.P.3.08 The TREAT-NMD Clinical Trials Coordination Centre (CTCC)

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.796-796

2008

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

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

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

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

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

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

Compound heterozygosity of the protein S-gene as a cause of severe cerebral sinovenous thrombosis in a 7-year-old child

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

Aicardi-Goutières-Syndrom: Seltene genetische Erkrankung imitiert intrauterine Virusinfektion

Peripheral Nerve Demyelination Caused by a Mutant Rho GTPase Guanine Nucleotide Exchange Factor, Frabin/FGD4

T.P.3.08 The TREAT-NMD Clinical Trials Coordination Centre (CTCC)

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