George W. Padberg

Nijmegen, GE, Netherlands

Last Updated: 09/26/2026

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Found 35 publications

A portrait of facioscapulohumeral muscular dystrophy through history: past milestones and future challenges on the road to understanding and treatment.

A portrait of facioscapulohumeral muscular dystrophy through history: past milestones and future challenges on the road to understanding and treatment.

Journal: Neuromuscular disorders : NMD
Published: December 30, 2025

26th Meryon Lecture St Anne's College, Oxford, 5th July 2024 FSHD: The long road to DUX4.

26th Meryon Lecture St Anne's College, Oxford, 5th July 2024 FSHD: The long road to DUX4.

Journal: Neuromuscular disorders : NMD
Published: September 10, 2024

The other face of facioscapulohumeral muscular dystrophy: Exploring orofacial weakness using muscle ultrasound.

The other face of facioscapulohumeral muscular dystrophy: Exploring orofacial weakness using muscle ultrasound.

Journal: Muscle & nerve
Published: December 01, 2023

Facioscapulohumeral Disease as a myodevelopmental disease: Applying Ockham's razor to its various features.

Facioscapulohumeral Disease as a myodevelopmental disease: Applying Ockham's razor to its various features.

Journal: Journal of neuromuscular diseases
Published: March 06, 2023

1st FSHD European Trial Network workshop:Working towards trial readiness across Europe.

1st FSHD European Trial Network workshop:Working towards trial readiness across Europe.

Journal: Neuromuscular disorders : NMD
Published: June 25, 2021

Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.

Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.

Journal: Nature genetics
Published: March 17, 2021

26th Annual Facioscapulohumeral Dystrophy International Research Congress Marseille, France, 19-20 June 2019.

26th Annual Facioscapulohumeral Dystrophy International Research Congress Marseille, France, 19-20 June 2019.

Journal: Neuromuscular disorders : NMD
Published: August 02, 2019

Ophthalmological findings in facioscapulohumeral dystrophy.

Ophthalmological findings in facioscapulohumeral dystrophy.

Journal: Brain communications
Published: July 03, 2019

Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations.

Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations.

Journal: Journal of neurology
Published: April 25, 2019

The Position of Neuromuscular Patients in Shared Decision Making. Report from the 235th ENMC Workshop: Milan, Italy, January 19-20, 2018.

The Position of Neuromuscular Patients in Shared Decision Making. Report from the 235th ENMC Workshop: Milan, Italy, January 19-20, 2018.

Journal: Journal of neuromuscular diseases
Published: February 05, 2019

"Be an ambassador for change that you would like to see": a call to action to all stakeholders for co-creation in healthcare and medical research to improve quality of life of people with a neuromuscular disease.

"Be an ambassador for change that you would like to see": a call to action to all stakeholders for co-creation in healthcare and medical research to improve quality of life of people with a neuromuscular disease.

Journal: Orphanet journal of rare diseases
Published: January 19, 2019

"The impact of European Neuromuscular Centre (ENMC) workshops on the neuromuscular field; 25 years on …".

"The impact of European Neuromuscular Centre (ENMC) workshops on the neuromuscular field; 25 years on …".

Journal: Neuromuscular disorders : NMD
Published: December 19, 2018
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Last Updated: 09/26/2026