Related references
Note: Only part of the references are listed.The genomic and clinical landscape of fetal akinesia
Matthias Pergande et al.
GENETICS IN MEDICINE (2020)
The latest FADS: Functional analysis of GLDN patient variants and classification of GLDN-associatedAMCas a type of viable fetal akinesia deformation sequence
Emily K. Mis et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2020)
Assisted Breathing with a Diaphragm Pacing System: A Systematic Review
A-la Woo et al.
YONSEI MEDICAL JOURNAL (2020)
Noninvasive Prediction of Twitch Transdiaphragmatic Pressure: Insights from Spirometry, Diaphragm Ultrasound, and Phrenic Nerve Stimulation Studies
Jens Spiesshoefer et al.
RESPIRATION (2019)
Survival among children with Lethal congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene (GLDN)
Jennifer A. Wambach et al.
HUMAN MUTATION (2017)
Twitch mouth pressure for detecting respiratory muscle weakness in suspicion of neuromuscular disorder
Dante Brasil Santos et al.
NEUROMUSCULAR DISORDERS (2017)
Mutations in GLDN, Encoding Gliomedin, a Critical Component of the Nodes of Ranvier, Are Responsible for Lethal Arthrogryposis
Jerome Maluenda et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2016)
Effects of respiratory muscle training on pulmonary functions in patients with slowly progressive neuromuscular disease: a randomized controlled trial
Goksen Kuran Aslan et al.
CLINICAL REHABILITATION (2014)
Pathophysiology of Hypoventilation During Sleep
Kenneth I. Berger et al.
SLEEP MEDICINE CLINICS (2014)
Antibodies to Gliomedin Cause Peripheral Demyelinating Neuropathy and the Dismantling of the Nodes of Ranvier
Jerome J. Devaux
AMERICAN JOURNAL OF PATHOLOGY (2012)
Gliomedin mediates Schwann cell-axon interaction and the molecular assembly of the nodes of Ranvier
Y Eshed et al.
NEURON (2005)