Martin G. Hausler
Aachen, NW, Germany
Last Updated: 09/26/2026
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Found 78 publications
Neuroborreliosis in children: Focus on ischemic stroke-a case report and literature review.
Journal: Klinische Padiatrie
Published: July 13, 2026
Interdisciplinary Clinical Practice Guidelines for patient-centred management of juvenile-onset systemic lupus erythematosus.
Journal: EULAR rheumatology open
Published: June 29, 2026
Clinical Impact of Ultrafast Cranial MRI Implementation in Children Under Six Years of Age.
Journal: Journal of clinical medicine
Published: December 29, 2025
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.
Journal: medRxiv : the preprint server for health sciences
Published: September 15, 2025
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.
Journal: Nature genetics
Published: September 02, 2025
Genetic Variants and Clinical Phenotyping in 39 Pediatric Patients with Neuropathic Pain.
Journal: Neuropediatrics
Published: April 28, 2025
Clinical phenotype and outcomes in autoimmune encephalitis after herpes simplex virus encephalitis: A systematic review and meta-analysis.
Journal: The Journal of infection
Published: April 25, 2025
Clinical presentation, MR imaging and outcome in children with myelin oligodendrocyte glycoprotein antibody-negative acute disseminated encephalomyelitis.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: January 29, 2025
Brain malformations and seizures by impaired chaperonin function of TRiC.
Journal: Science (New York, N.Y.)
Published: October 31, 2024
Characterization of children with early onset pediatric multiple sclerosis.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: August 17, 2024
HNRNPA1 de novo Variant Associated with Early Childhood Onset, Rapidly Progressive Generalized Myopathy.
Journal: Journal of neuromuscular diseases
Published: August 09, 2024
Biallelic pathogenic hydroxymethylbilane synthase gene variants of a neurodegenerative disorder with progressive cystic leukoencephalopathy: a case report.
Journal: Journal of medical case reports
Published: June 08, 2024
Last Updated: 09/26/2026