Myosin storage myopathy: slow skeletal myosin (MYH7) mutation in two isolated cases
Laing, N G, Ceuterick-de Groote, C, Dye, D E, Liyanage, K, Duff, R M, Dubois, B, Robberecht, W, Sciot, R, Martin, J-J, Goebel, H H
Published in Neurology (08.02.2005)
Published in Neurology (08.02.2005)
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Journal Article
Fabry disease in a patient with Turner syndrome
Brouns, R., Eyskens, F., De Boeck, K., Ceuterick-de Groote, C., Van den Broeck, M., Van Broeckhoven, C., De Deyn, P. P.
Published in Journal of inherited metabolic disease (01.12.2009)
Published in Journal of inherited metabolic disease (01.12.2009)
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A novel mitochondrial transfer RNA proline mutation
Seneca, S., Lissens, W., Ceuterick‐De Groote, C., Van Coster, R., De Meirleir, L.
Published in Journal of inherited metabolic disease (01.12.2000)
Published in Journal of inherited metabolic disease (01.12.2000)
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Journal Article
Compound RYR1 heterozygosity resulting in a complex phenotype of malignant hyperthermia susceptibility and a core myopathy
Kraeva, N, Heytens, L, Jungbluth, H, Treves, S, Voermans, N, Kamsteeg, E, Ceuterick-de Groote, C, Baets, J, Riazi, S
Published in Neuromuscular disorders : NMD (01.07.2015)
Published in Neuromuscular disorders : NMD (01.07.2015)
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Journal Article
Linezolid-Induced Inhibition of Mitochondrial Protein Synthesis
De Vriese, An S., Van Coster, Rudy, Smet, Joél, Seneca, Sara, Lovering, Andrew, Van Haute, Lindsey L., Vanopdenbosch, Ludo J., Martin, Jean-Jacques, Ceuterick-de Groote, Chantal, Vandecasteele, Stefaan, Boelaert, Johan R.
Published in Clinical infectious diseases (15.04.2006)
Published in Clinical infectious diseases (15.04.2006)
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Early-onset dementia, leukoencephalopathy and brain calcifications: a clinical, imaging and pathological comparison of ALSP and PLOSL/Nasu Hakola disease
Coomans, C., Sieben, A., Lammens, M., Ceuterick-de Groote, C., Vandenbroecke, C., Goethals, I., Van Melkebeke, D., Hemelsoet, D.
Published in Acta neurologica Belgica (01.12.2018)
Published in Acta neurologica Belgica (01.12.2018)
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Journal Article
Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency
Guergueltcheva, V, Peeters, K, Baets, J, Ceuterick-de Groote, C, Martin, J J, Suls, A, De Vriendt, E, Mihaylova, V, Chamova, T, Almeida-Souza, L, Ydens, E, Tzekov, C, Hadjidekov, G, Gospodinova, M, Storm, K, Reyniers, E, Bichev, S, van der Ven, P F M, Fürst, D O, Mitev, V, Lochmüller, H, Timmerman, V, Tournev, I, De Jonghe, P, Jordanova, A
Published in Neurology (13.12.2011)
Published in Neurology (13.12.2011)
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Journal Article
OP10 – 2707: Childhood-onset ataxic gait solved by muscle biopsy
Jansen, A, Ceuterick-de Groote, C, Vanderhasselt, T, Seneca, S, Stouffs, K, De Meirleir, L
Published in European journal of paediatric neurology (01.05.2015)
Published in European journal of paediatric neurology (01.05.2015)
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A new combined Bodian-Luxol technique for staining unmyelinated axons in semithin, resin-embedded peripheral nerves : a comparison with electron microscopy
DEPREZ, M, CEUTERICK-DE GROOTE, C, FUMAL, A, REZNIK, M, MARTIN, J. J
Published in Acta neuropathologica (01.10.1999)
Published in Acta neuropathologica (01.10.1999)
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P3.36. Phenotypic spectrum in myopathies with tubular aggregates
Funk, F, Ceuterick-de Groote, C, Martin, J.J, Meinhardt, A, de Bleecker, J, de Jonghe, P, Taratuto, A.L, Saccoliti, M, Schröder, J.M, Schulz, J.B, Weis, J, Claeys, K.G
Published in Neuromuscular disorders : NMD (01.10.2011)
Published in Neuromuscular disorders : NMD (01.10.2011)
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Journal Article
G.O.7 Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency
Guergueltcheva, V, Peeters, K, Baets, J, Ceuterick-de Groote, C, Martin, J.J, Suls, A, Vriendt, E.D, Mihaylova, V, Chamova, T, Almeida-Souza, L, Ydens, E, Tzekov, C, Hadjidekov, G, Gospodinova, M, Storm, K, Reyniers, E, Bichev, S, van der Ven, P.F.M, Furst, D.O, Mitev, V, Lochmuller, H, Timmerman, V, Tournev, I, De Jonghe, P, Jordanova, A
Published in Neuromuscular disorders : NMD (01.10.2012)
Published in Neuromuscular disorders : NMD (01.10.2012)
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P245 ROUX-EN-Y GASTRIC BYPASS ATTENUATES HEPATIC MITOCHONDRIAL DYSFUNCTION IN MICE WITH NONALCOHOLIC STEATOHEPATITIS
Verbeek, J, Lannoo, M, Pirinen, E, Ryu, D, Spincemaille, P, Elst, I. Vander, Windmolders, P, Thevissen, K, Cammue, B.P.A, van Pelt, J, Ceuterick-De Groote, C, Van Veldhoven, P.P, Bedossa, P, Nevens, F, Cassiman, D
Published in Journal of hepatology (01.04.2014)
Published in Journal of hepatology (01.04.2014)
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Journal Article
Clinical and neuropathological parameters affecting the diagnostic yield of nerve biopsy
Deprez, M, de Groote, C C, Gollogly, L, Reznik, M, Martin, J J
Published in Neuromuscular disorders : NMD (01.02.2000)
Published in Neuromuscular disorders : NMD (01.02.2000)
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Infantile Demyelinating Neuropathy Associated with a de novo Point Mutation on Ser72 in PMP22 and Basal Lamina Onion Bulbs in Skin Biopsy
Ceuterick-de Groote, C., De Jonghe, P., De Jonghe, P., Timmerman, V., Van Goethem, G., Löfgren, A., Ceulemans, B., Van Broeckhoven, C., Martin, J.-J., Martin, J.-J.
Published in Pathology, research and practice (2001)
Published in Pathology, research and practice (2001)
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Journal Article
Nerve biopsy: indications and contribution to the diagnosis of peripheral neuropathy. The experience of the Born Bunge Foundation University of Antwerp and University of Liege between 1987 and 1997
Deprez, M, Ceuterick-de Groote, C, Schoenen, J, Reznik, M, Martin, J J
Published in Acta neurologica Belgica (01.09.2000)
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Published in Acta neurologica Belgica (01.09.2000)
Journal Article
An unusual, common(?) finding in skeletal muscle biopsies
Published in Ultrastructural pathology
(2000)
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Journal Article
Malignant pigmented spinal nerve root schwannoma metastasizing in the brain and viscera
Cras, P, Ceuterick-de Groote, C, Van Vyve, M, Vercruyssen, A, Martin, J J
Published in Clinical neuropathology (01.11.1990)
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Published in Clinical neuropathology (01.11.1990)
Journal Article
P201 – 1718 Twins with remarkable stereotypical hand movements
Van Ingelghem, I, Hellinckx, J, Wojciechowski, M, Matthijs, G, Ceuterick-de Groote, C, Ceulemans, B
Published in European journal of paediatric neurology (01.09.2013)
Published in European journal of paediatric neurology (01.09.2013)
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Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IV
Verpoorten, Nathalie, Claeys, Kristl G., Deprez, Liesbet, Jacobs, An, Gerwen, Veerle Van, Lagae, Lieven, Arts, Willem Frans, Meirleir, Linda De, Keymolen, Kathelijn, Groote, Chantal Ceuterick-de, Jonghe, Peter De, Timmerman, Vincent, Nelis, Eva
Published in Neuromuscular disorders : NMD (01.01.2006)
Published in Neuromuscular disorders : NMD (01.01.2006)
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Journal Article
Clinical And Neuropathological Parameters Affecting The Diagnostic Yield Of Nerve Biopsy
Deprez, M., Ceuterick‐de Groote, C., Gollogly, L., Reznik, M., Martin, J.J.
Published in Journal of the peripheral nervous system (01.06.2000)
Published in Journal of the peripheral nervous system (01.06.2000)
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