Peter Huppke
Jena, TH, Germany
Last Updated: 09/26/2026
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Found 75 publications
Serum neurofilament light chain in paediatric patients treated with natalizumab for highly active multiple sclerosis.
Journal: Multiple sclerosis (Houndmills, Basingstoke, England)
Published: June 23, 2026
Real-world practices and challenges of radiologically isolated syndrome: results of a cross-sector survey by the DACH MS guidelines group.
Journal: Frontiers in neurology
Published: March 04, 2026
Not all acute peripheral facial palsy in children recovers completely: A telediagnostic follow-up study.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: February 23, 2026
Decreased skull growth in positional plagiocephaly patients undergoing helmet therapy.
Journal: Brain & spine
Published: October 09, 2025
Acute changes in gait biomechanics in children with cerebral palsy due to barefoot vs. footwear condition - An exploratory study.
Journal: Clinical biomechanics (Bristol, Avon)
Published: September 09, 2025
The Inner Nuclear Layer in Pediatric Multiple Sclerosis.
Journal: Neurology(R) neuroimmunology & neuroinflammation
Published: May 08, 2025
The Inner Nuclear Layer in Pediatric Multiple Sclerosis.
Journal: Neurology(R) neuroimmunology & neuroinflammation
Published: March 26, 2025
Biallelic ELOVL1 Variants Are Linked to Hypomyelinating Leukodystrophy, Movement Disorder, and Ichthyosis.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: March 18, 2025
Severe Disease Activation after Fingolimod Discontinuation in a Pediatric Multiple Sclerosis Patient: A Case Report and Literature Review.
Journal: Neuropediatrics
Published: December 05, 2024
Rett Syndrome: Specific MECP2 Variants are Associated With Elevated Serum Neurofilament Light Chain.
Rett Syndrome: Specific MECP2 Variants are Associated With Elevated Serum Neurofilament Light Chain.
Journal: Pediatric neurology
Published: August 09, 2024
De novo AHDC1 Deletions Identified by Genome Sequencing in Two Individuals with Xia-Gibbs Syndrome.
Journal: Molecular syndromology
Published: November 14, 2023
Long term follow-up in GAMT deficiency - Correlation of therapy regimen, biochemical and in vivo brain proton MR spectroscopy data.
Journal: Molecular genetics and metabolism reports
Published: November 04, 2023
Last Updated: 09/26/2026