L. Eshuis

Human Intellectual Disability Genes Form Conserved Functional Modules in Drosophila

M. Huynen, P. Verstreken, Shivakumar Keerthikumar, 2013, PLoS genetics.

Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33

E. Mariman, F. Gabreëls, B. V. van Engelen, 1999, Journal of neurology, neurosurgery, and psychiatry.

Mild Muscular Features in Tenascin-X Knockout Mice, A Model of Ehlers–Danlos Syndrome

J. A. van der Laak, I. V. van Rooij, B. V. van Engelen, 2011, Connective tissue research.

Superior preservation of capillaries, myofibrils and mitochondria after long-term extracorporeal perfusion of free muscle flaps – A descriptive electron microscopy study

L. Eshuis, S. Hummelink, D. Ulrich, 2022, Clinical hemorheology and microcirculation.

The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations

J. Holton, B. Küsters, N. Voermans, 2019, Journal of Neurology.

Dystrophic Myopathy of the Diaphragm with Recurrent Severe Respiratory Failure is Congenital Myasthenic Syndrome 11

B. Eymard, N. Voermans, L. Eshuis, 2022, Journal of neuromuscular diseases.

Mild Muscular Features in Tenascin-X Knockout Mice, A Model of Ehlers–Danlos Syndrome

K. Verrijp, N. Voermans, L. Eshuis, 2011, Connective tissue research.