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J Baets

Showing results (1-10 of 15) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|February 21, 2009
An extensive spinal epidural abscess successfully treated conservativelyJ Van Bergen, M Plazier, J Baets, et al.
Acta Neurologica Belgica|November 10, 2006
Opsoclonus-myoclonus syndrome: a clinicopathological confrontationJ Baets, P Pals, B Bergmans, et al.
Journal of the Neurological Sciences|July 6, 2010
N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndromeV Rakocević-Stojanović, V Milić-Rasić, S Perić, et al.
Neuromuscular Disorders : NMD|May 11, 2015
Compound RYR1 heterozygosity resulting in a complex phenotype of malignant hyperthermia susceptibility and a core myopathyN Kraeva, L Heytens, H Jungbluth, et al.
Journal of Neuromuscular Diseases|April 25, 2025
Liver function in X-linked myotubular myopathy and autosomal dominant centronuclear myopathy: Data of the unite-CNM studyS Colombo, B S Cowling, L Eyler, et al.
Orphanet Journal of Rare Diseases|April 7, 2020
Late-onset Pompe disease (LOPD) in Belgium: clinical characteristics and outcome measuresP Vanherpe, S Fieuws, A D'Hondt, et al.
Neurology|September 30, 2010
Mutations in SACS cause atypical and late-onset forms of ARSACSJ Baets, T Deconinck, K Smets, et al.
European Journal of Neurology|March 20, 2010
EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementiasJ-M Burgunder, J Finsterer, Z Szolnoki, et al.
European Journal of Neurology|May 27, 2010
EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disordersJ-M Burgunder, L Schöls, J Baets, et al.
European Journal of Neurology|May 28, 2009
EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystoniasH F Harbo, J Finsterer, J Baets, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Journal of Neurology, Neurosurgery, and Psychiatry|February 21, 2009
An extensive spinal epidural abscess successfully treated conservativelyJ Van Bergen, M Plazier, J Baets, et al.
Acta Neurologica Belgica|November 10, 2006
Opsoclonus-myoclonus syndrome: a clinicopathological confrontationJ Baets, P Pals, B Bergmans, et al.
Journal of the Neurological Sciences|July 6, 2010
N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndromeV Rakocević-Stojanović, V Milić-Rasić, S Perić, et al.
Neuromuscular Disorders : NMD|May 11, 2015
Compound RYR1 heterozygosity resulting in a complex phenotype of malignant hyperthermia susceptibility and a core myopathyN Kraeva, L Heytens, H Jungbluth, et al.
Journal of Neuromuscular Diseases|April 25, 2025
Liver function in X-linked myotubular myopathy and autosomal dominant centronuclear myopathy: Data of the unite-CNM studyS Colombo, B S Cowling, L Eyler, et al.
Orphanet Journal of Rare Diseases|April 7, 2020
Late-onset Pompe disease (LOPD) in Belgium: clinical characteristics and outcome measuresP Vanherpe, S Fieuws, A D'Hondt, et al.
Neurology|September 30, 2010
Mutations in SACS cause atypical and late-onset forms of ARSACSJ Baets, T Deconinck, K Smets, et al.
European Journal of Neurology|March 20, 2010
EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementiasJ-M Burgunder, J Finsterer, Z Szolnoki, et al.
European Journal of Neurology|May 27, 2010
EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disordersJ-M Burgunder, L Schöls, J Baets, et al.
European Journal of Neurology|May 28, 2009
EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystoniasH F Harbo, J Finsterer, J Baets, et al.
Pageof 2