Rudolf Korinthenberg

Freiburg, BW, Germany

Last Updated: 09/26/2026

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Found 58 publications

Disease characteristics of SEPSECS deficiency: an international, retrospective, multicenter cohort study.

Disease characteristics of SEPSECS deficiency: an international, retrospective, multicenter cohort study.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: April 02, 2025

Efficacy and safety of corticosteroids and ACTH in epileptic syndromes beyond Infantile Epileptic Spasms Syndrome (IESS): A systematic review and meta-analysis.

Efficacy and safety of corticosteroids and ACTH in epileptic syndromes beyond Infantile Epileptic Spasms Syndrome (IESS): A systematic review and meta-analysis.

Journal: Epilepsia

Published: December 06, 2023

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.

Journal: medRxiv : the preprint server for health sciences

Published: March 03, 2023

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

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

Journal: Neuropediatrics

Published: December 21, 2022

Predicting respiratory failure and outcome in pediatric Guillain-Barré syndrome.

Predicting respiratory failure and outcome in pediatric Guillain-Barré syndrome.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: October 09, 2022

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

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

Journal: Neuropediatrics

Published: July 26, 2022

Special Issue "Neuromuscular Disorders in Children and Adolescents".

Special Issue "Neuromuscular Disorders in Children and Adolescents".

Journal: Children (Basel, Switzerland)

Published: January 14, 2022

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

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

Journal: Children (Basel, Switzerland)

Published: June 28, 2021

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

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

Journal: Neuropediatrics

Published: October 28, 2020

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

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

Journal: Neuropediatrics

Published: October 21, 2020

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

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

Journal: Journal of the peripheral nervous system : JPNS

Published: August 14, 2020

Agammaglobulinemia with normal B-cell numbers in a patient lacking Bob1.

Agammaglobulinemia with normal B-cell numbers in a patient lacking Bob1.

Journal: The Journal of allergy and clinical immunology

Published: June 05, 2020

Showing 1-12 of 58

Last Updated: 09/26/2026