Thomas K. Volkl
Augsburg, BY, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
Protein-truncating variants in APBA1 in minors with severe, early-onset obesity: implications for genetic testing.
Journal: Molecular and cellular pediatrics
Published: January 15, 2026
Correction: Development of a standardized handover for critically ill premature and newborn infants for interhospital transport in Bavaria
Journal: Zeitschrift fur Geburtshilfe und Neonatologie
Published: December 09, 2025
Clinical and Biochemical Monitoring of Monocarboxylate Transporter 8 Deficiency (Allan-Herndon-Dudley Syndrome) across the Lifespan: Practical Considerations for Multidisciplinary Care.
Journal: Hormone research in paediatrics
Published: October 28, 2025
Development of a standardized handover for critically ill premature and newborn infants for interhospital transport in Bavaria
Journal: Zeitschrift fur Geburtshilfe und Neonatologie
Published: August 01, 2025
Automatic versus manual control of oxygen and neonatal clinical outcomes in extremely preterm infants: a multicentre, parallel-group, randomised, controlled, superiority trial.
Journal: The Lancet. Child & adolescent health
Published: July 17, 2025
Swallowing Assessment in a Pediatric Case of Allan-Herndon-Dudley Syndrome (MCT8 Deficiency): Advanced Insights into Dysphagia via Flexible Endoscopic Evaluation of Swallowing.
Journal: Neuropediatrics
Published: December 16, 2024
Treatment of severe traumatic brain injury in German pediatric intensive care units-a survey of current practice.
Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: February 05, 2019
Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency
Journal: Journal of clinical research in pediatric endocrinology
Published: September 05, 2018
Showing 1-10 of 10
Last Updated: 09/26/2026