Rudolf Korinthenberg

Professor, Ärztl. Direktor Neuropädiatrie

Albert-Ludwigs-Universität Freiburg

Germany

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Articles (8)

Year:

2023

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2020

Collaborators (6)

Joachim Weis

Medizinische Fakultät der RWTH Aachen

GERMANY

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Martin Häusler

RWTH Aachen University

GERMANY

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Sarah C. Grünert

University Medical Center

GERMANY

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Georg M. Stettner

Head of Neuromuscular Center

University Children's Hospital Zurich

SWITZERLAND

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Barbara Plecko

SWITZERLAND

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Robert Steinfeld

SWITZERLAND

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Rudolf Korinthenberg

Research Interests

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Articles (8)

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

Treatment of Infantile Spasm Syndrome: Update from the Interdisciplinary Guideline Committee Coordinated by the German-Speaking Society of Neuropediatrics

Special Issue “Neuromuscular Disorders in Children and Adolescents”

Alpers- and MNGIE-like disease with disturbed CSF folate transport and an unusual mode of genetic transmission of POLG mutations: a case report

Differential Diagnosis of Acquired and Hereditary Neuropathies in Children and Adolescents—Consensus-Based Practice Guidelines

Thiamine Treatment and Favorable Outcome in an Infant with Biallelic TPK1 Variants

Severe Locked-In-Like Guillain–Barré's Syndrome: Dilemmas in Diagnosis and Treatment

The Brighton Collaboration case definition: Comparison in a retrospective and prospective cohort of children with Guillain‐Barré syndrome

Collaborators (6)

Joachim Weis

Martin Häusler

Sarah C. Grünert

Georg M. Stettner

Barbara Plecko

Robert Steinfeld

Make your next move.

Rudolf Korinthenberg

Research Interests

Explore related searches

Contact this professor

Articles (8)

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

Treatment of Infantile Spasm Syndrome: Update from the Interdisciplinary Guideline Committee Coordinated by the German-Speaking Society of Neuropediatrics

Special Issue &ldquo;Neuromuscular Disorders in Children and Adolescents&rdquo;

Alpers- and MNGIE-like disease with disturbed CSF folate transport and an unusual mode of genetic transmission of POLG mutations: a case report

Differential Diagnosis of Acquired and Hereditary Neuropathies in Children and Adolescents—Consensus-Based Practice Guidelines

Thiamine Treatment and Favorable Outcome in an Infant with Biallelic TPK1 Variants

Severe Locked-In-Like Guillain–Barré's Syndrome: Dilemmas in Diagnosis and Treatment

The Brighton Collaboration case definition: Comparison in a retrospective and prospective cohort of children with Guillain‐Barré syndrome

Collaborators (6)

Joachim Weis

Martin Häusler

Sarah C. Grünert

Georg M. Stettner

Barbara Plecko

Robert Steinfeld

Make your next move.

Special Issue “Neuromuscular Disorders in Children and Adolescents”