Iris Hannibal

Dr. Von Hauner Children's Hospital
Munich, BY, Germany

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 23 publications

Between myopathy and mortality: Challenges in the diagnosis of PLOD1-related kyphoscoliotic Ehlers-Danlos syndrome.

Between myopathy and mortality: Challenges in the diagnosis of PLOD1-related kyphoscoliotic Ehlers-Danlos syndrome.

Journal: Journal of neuromuscular diseases

Published: August 29, 2026

Functional disease progression in children with inherited peripheral neuropathies: A prospective cohort study.

Functional disease progression in children with inherited peripheral neuropathies: A prospective cohort study.

Journal: Journal of neuromuscular diseases

Published: July 03, 2026

From genotype to outcome: Zygosity-specific insights in 63 cases of CLPB-related mitochondrial disease.

From genotype to outcome: Zygosity-specific insights in 63 cases of CLPB-related mitochondrial disease.

Journal: Molecular genetics and metabolism

Published: November 25, 2025

Long-Term Socioeconomic and Neurologic Outcome for Individuals with Childhood-Onset Multiple Sclerosis.

Long-Term Socioeconomic and Neurologic Outcome for Individuals with Childhood-Onset Multiple Sclerosis.

Journal: Children (Basel, Switzerland)

Published: July 22, 2024

Neuromodulation in Pediatric Migraine using Repetitive Neuromuscular Magnetic Stimulation: A Feasibility Study.

Neuromodulation in Pediatric Migraine using Repetitive Neuromuscular Magnetic Stimulation: A Feasibility Study.

Journal: Children (Basel, Switzerland)

Published: September 26, 2023

De novo variants in GATAD2A in individuals with a neurodevelopmental disorder: GATAD2A-related neurodevelopmental disorder.

De novo variants in GATAD2A in individuals with a neurodevelopmental disorder: GATAD2A-related neurodevelopmental disorder.

Journal: HGG advances

Published: January 17, 2023

Newbornscreening SMA - From Pilot Project to Nationwide Screening in Germany.

Newbornscreening SMA - From Pilot Project to Nationwide Screening in Germany.

Journal: Journal of neuromuscular diseases

Published: December 04, 2022

ARF1-related disorder: phenotypic and molecular spectrum.

ARF1-related disorder: phenotypic and molecular spectrum.

Journal: Journal of medical genetics

Published: August 09, 2022

Newborn Screening for SMA - Can a Wait-and-See Strategy be Responsibly Justified in Patients With Four SMN2 Copies?

Newborn Screening for SMA - Can a Wait-and-See Strategy be Responsibly Justified in Patients With Four SMN2 Copies?

Journal: Journal of neuromuscular diseases

Published: July 18, 2022

Repetitive Neuromuscular Magnetic Stimulation for Pediatric Headache Disorders: Muscular Effects and Factors Affecting Level of Response.

Repetitive Neuromuscular Magnetic Stimulation for Pediatric Headache Disorders: Muscular Effects and Factors Affecting Level of Response.

Journal: Brain sciences

Published: June 09, 2022

Repetitive neuromuscular magnetic stimulation in children with headache.

Repetitive neuromuscular magnetic stimulation in children with headache.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: January 19, 2022

Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency.

Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: July 24, 2021

Showing 1-12 of 23

Last Updated: 09/26/2026