Sandy Siegert
Vienna, Austria
Last Updated: 09/26/2026
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Found 20 publications
Beyond the interferon score: neurofilament light chain and glial fibrillary acidic protein capture immune-mediated neuroinjury and response to JAK inhibition in Aicardi-Goutières syndrome.
Journal: Frontiers in immunology
Published: January 06, 2026
KMT2B-related disorders in Austria: clinical features and long-term outcome after deep brain stimulation.
Journal: Frontiers in neurology
Published: October 18, 2025
Complications of Therapeutic Plasma Exchange in Pediatric Neuroimmune Disorders.
Journal: Children (Basel, Switzerland)
Published: September 10, 2025
Acute flaccid myelitis in Europe between 2016 and 2023: indicating the need for better registration.
Acute flaccid myelitis in Europe between 2016 and 2023: indicating the need for better registration.
Journal: Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin
Published: May 30, 2025
Achondroplasia : New era of orthopedic treatment?
Journal: Orthopadie (Heidelberg, Germany)
Published: October 16, 2024
CSF-profile and hypocretin levels in children with narcolepsy type 1 and 2.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: May 03, 2024
Improving paediatric movement disorders care: Insights on rating scales utilization and clinical practice.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: April 27, 2024
Developmental, Cognitive, Ocular Motor, and Neuroimaging Findings Related to SUFU Haploinsufficiency: Unraveling Subtle and Highly Variable Phenotypes.
Journal: Pediatric neurology
Published: January 14, 2024
Rituximab treatment in pediatric-onset multiple sclerosis.
Journal: European journal of neurology
Published: September 08, 2023
Episignature analysis of moderate effects and mosaics.
Journal: European journal of human genetics : EJHG
Published: January 30, 2023
A De Novo Missense NPTX1 Variant in an Individual with Infantile-Onset Cerebellar Ataxia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: April 12, 2022
Last Updated: 09/26/2026