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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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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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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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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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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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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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Dopa-responsive dystonia: Mutation analysis of GCH1 and analysis of therapeutic doses of l -dopa

Neurology, 2000-12, Vol.55 (11), p.1735-1738

2000

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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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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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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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Supra- and Infratentorial Atrophy with Cortical Blindness Caused by Mutations in SEPSECS: Case Report

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

2017

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Progressive Radial Motor Neuropathy Due to a Perineurioma in an Adolescent Girl: Case Report

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

2017

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Muscle Dystrophy Differential Diagnosis: Manifestation of Anti-HMG-CoA Reductase Antibody Myositis in Infancy

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

2017

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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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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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Chronic Hemolysis, Steroid-Dependent CIDP, and Progressive Moya-Moya Disease Due to Hereditary Immune Dysregulation

Neuropediatrics, 2016, Vol.47 (S 01)

2016

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Rare Case of Miller-Fisher Syndrome

Neuropediatrics, 2016, Vol.47 (S 01)

2016

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P097 A new locus for an autosomal recessive congenital muscular dystrophy without brain involvement maps to chromosome 7p21

European journal of paediatric neurology, 2009, Vol.13, p.S51-S51

2009

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P.77 - 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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Severe Neonatal Apnea Episodes Associated with a Nondystrophic Congenital Myotonia Caused by a Mutation in the Gene SCN4A

Neuropediatrics, 2015, Vol.46 (S 01)

2015

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West Syndrome in Hypothalamic Hamartoma: A Rare Clinical Presentation

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

2017

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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

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

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

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?

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

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

Dopa-responsive dystonia: Mutation analysis of GCH1 and analysis of therapeutic doses of l -dopa

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

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

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

Supra- and Infratentorial Atrophy with Cortical Blindness Caused by Mutations in SEPSECS: Case Report

Progressive Radial Motor Neuropathy Due to a Perineurioma in an Adolescent Girl: Case Report

Muscle Dystrophy Differential Diagnosis: Manifestation of Anti-HMG-CoA Reductase Antibody Myositis in Infancy

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

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

Chronic Hemolysis, Steroid-Dependent CIDP, and Progressive Moya-Moya Disease Due to Hereditary Immune Dysregulation

Rare Case of Miller-Fisher Syndrome

P097 A new locus for an autosomal recessive congenital muscular dystrophy without brain involvement maps to chromosome 7p21

P.77 - Severe congenital myopathy with myasthenic features and lethal neurodegeneration – A new ALG14-related phenotype?

Severe Neonatal Apnea Episodes Associated with a Nondystrophic Congenital Myotonia Caused by a Mutation in the Gene SCN4A

West Syndrome in Hypothalamic Hamartoma: A Rare Clinical Presentation

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