Andrea Bevot

Hoppe Seyler Str. 3
Tuebingen, BW 72076, Germany

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 68 publications

Insights into Accelerated MRI Protocols for Pediatric Brain Assessment in Emergency Cases.

Insights into Accelerated MRI Protocols for Pediatric Brain Assessment in Emergency Cases.

Journal: Diagnostics (Basel, Switzerland)

Published: January 09, 2026

Markerless gait analysis for children and adolescents with juvenile idiopathic arthritis using a machine learning pipeline.

Markerless gait analysis for children and adolescents with juvenile idiopathic arthritis using a machine learning pipeline.

Journal: Pediatric rheumatology online journal

Published: September 27, 2025

Phenotypic intrafamilial variability of 5q-associated spinal muscular atrophy: A systematic multicentre sibling study.

Phenotypic intrafamilial variability of 5q-associated spinal muscular atrophy: A systematic multicentre sibling study.

Journal: Journal of neuromuscular diseases

Published: September 12, 2025

Prevalence of sleep-related breathing disorders in children with myelomeningocele and other spinal dysraphisms and risk factors.

Prevalence of sleep-related breathing disorders in children with myelomeningocele and other spinal dysraphisms and risk factors.

Journal: Sleep medicine

Published: September 09, 2025

The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency.

The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency.

Journal: Brain : a journal of neurology

Published: July 01, 2025

The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency.

The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency.

Journal: Brain : a journal of neurology

Published: July 01, 2025

Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

Journal: Nature genetics

Published: June 24, 2025

Encephalitis Unraveled: The Unlikely Encounter of Sickle Cell Disease and Cerebral Malaria in a Teenager.

Encephalitis Unraveled: The Unlikely Encounter of Sickle Cell Disease and Cerebral Malaria in a Teenager.

Journal: Diagnostics (Basel, Switzerland)

Published: April 22, 2025

Case Report: Post-surgical Guillain-Barré syndrome as a rare differential diagnosis of flaccid paralysis of the lower extremities in an infant after cardiac surgery.

Case Report: Post-surgical Guillain-Barré syndrome as a rare differential diagnosis of flaccid paralysis of the lower extremities in an infant after cardiac surgery.

Journal: Frontiers in pediatrics

Published: April 11, 2025

Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.

Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.

Journal: Nature communications

Published: March 31, 2025

Effects of Pallidal Deep Brain Stimulation on Speech and Swallowing in Pediatric Patients with Dystonia.

Effects of Pallidal Deep Brain Stimulation on Speech and Swallowing in Pediatric Patients with Dystonia.

Journal: Movement disorders clinical practice

Published: March 07, 2025

Protracted Febrile Illness and Coma in an Adolescent with Sickle Cell Disease and Malaria.

Protracted Febrile Illness and Coma in an Adolescent with Sickle Cell Disease and Malaria.

Journal: The American journal of tropical medicine and hygiene

Published: February 10, 2025

Showing 1-12 of 68

Last Updated: 09/26/2026