
Regina Trollmann
Erlangen, BY, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 135 publications
Delphi consensus on gene therapy of spinal muscular atrophy with onasemnogene abeparvovec in Germany, Austria and Switzerland - part II - expert based recommendations for surveillance and management of side-effects.
Journal: Journal of neuromuscular diseases
Published: August 27, 2026
Effects of Lipid-Induced Magnetic Microstructure on Fat Fraction Quantification in Muscular Dystrophies.
Journal: Magnetic resonance in medicine
Published: May 04, 2026
The clinical picture of symptomatic Rathke cleft cysts in children.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: April 28, 2026
Somatosensory evoked fields at 36 weeks' gestation in preterm infants: A pilot study of thalamocortical maturation.
Journal: Clinical neurophysiology practice
Published: March 24, 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
A multi-omics approach to characterize a deep intronic ARID1A deletion in Coffin-Siris syndrome.
Journal: European journal of medical genetics
Published: February 06, 2026
Delphi consensus on gene therapy of spinal muscular atrophy with onasemnogene abeparvovec in Germany, Austria and Switzerland-part I-systematic literature review and existing evidence.
Journal: Journal of neuromuscular diseases
Published: November 24, 2025
Longitudinal functional lung imaging in children with Post-COVID-19 syndrome.
Journal: Molecular and cellular pediatrics
Published: October 07, 2025
Phenotypic intrafamilial variability of 5q-associated spinal muscular atrophy: A systematic multicentre sibling study.
Journal: Journal of neuromuscular diseases
Published: September 12, 2025
Challenges of Standard Pediatric Epilepsy Monitoring and the Potential Benefits of Contactless Sensor Technologies: Exploratory Qualitative Study.
Journal: Journal of medical Internet research
Published: August 26, 2025
Missense Variants in the A Isoform of FGF13 as a Novel Cause of Paroxysmal Dyskinesia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: July 28, 2025
The clinical picture of symptomatic Rathke cleft cysts in children.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: July 20, 2025
Last Updated: 09/26/2026