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C Ceuterick

Showing results (71-80 of 92) with videos related to

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Archives of Neurology|October 16, 1999
A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotypeP De Jonghe, V Timmerman, E Nelis, et al.
Brain Research|February 19, 1993
Rimmed vacuoles of inclusion body myositis and oculopharyngeal muscular dystrophy contain amyloid precursor protein and lysosomal markersM Villanova, M Kawai, U Lübke, 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.
Human Molecular Genetics|July 1, 1996
Distal hereditary motor neuropathy type II (distal HMN II): mapping of a locus to chromosome 12q24V Timmerman, P De Jonghe, S Simokovic, et al.
Journal of Inherited Metabolic Disease|April 4, 2009
Fabry disease in a patient with Turner syndromeR Brouns, F Eyskens, K De Boeck, et al.
Neurology|January 1, 1991
Early-onset Alzheimer's disease in 2 large Belgian familiesJ J Martin, J Gheuens, M Bruyland, et al.
Pathology, Research and Practice|April 21, 2001
Infantile demyelinating neuropathy associated with a de novo point mutation on Ser72 in PMP22 and basal lamina onion bulbs in skin biopsyC Ceuterick-de Groote, P De Jonghe, V Timmerman, et al.
Journal of the Neurological Sciences|April 1, 1988
Defect in succinate oxidation by isolated muscle mitochondria in a patient with symmetrical lesions in the basal gangliaJ J Martin, F L Van de Vyver, H R Scholte, et al.
Brain Research|August 30, 1991
Demonstration of a novel neurofilament associated antigen with the neurofibrillary pathology of Alzheimer and related diseasesJ Gheuens, P Cras, G Perry, et al.
Revue Neurologique|June 20, 2002
[Hereditary neuropathy with liability to pressure palsies: study of six Spanish families]A Pou Serradell, J Monells, M J Téllez, et al.
Pageof 10

Showing results (71-80 of 92) with videos related to

Sort By:
Pageof 10
Archives of Neurology|October 16, 1999
A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotypeP De Jonghe, V Timmerman, E Nelis, et al.
Brain Research|February 19, 1993
Rimmed vacuoles of inclusion body myositis and oculopharyngeal muscular dystrophy contain amyloid precursor protein and lysosomal markersM Villanova, M Kawai, U Lübke, 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.
Human Molecular Genetics|July 1, 1996
Distal hereditary motor neuropathy type II (distal HMN II): mapping of a locus to chromosome 12q24V Timmerman, P De Jonghe, S Simokovic, et al.
Journal of Inherited Metabolic Disease|April 4, 2009
Fabry disease in a patient with Turner syndromeR Brouns, F Eyskens, K De Boeck, et al.
Neurology|January 1, 1991
Early-onset Alzheimer's disease in 2 large Belgian familiesJ J Martin, J Gheuens, M Bruyland, et al.
Pathology, Research and Practice|April 21, 2001
Infantile demyelinating neuropathy associated with a de novo point mutation on Ser72 in PMP22 and basal lamina onion bulbs in skin biopsyC Ceuterick-de Groote, P De Jonghe, V Timmerman, et al.
Journal of the Neurological Sciences|April 1, 1988
Defect in succinate oxidation by isolated muscle mitochondria in a patient with symmetrical lesions in the basal gangliaJ J Martin, F L Van de Vyver, H R Scholte, et al.
Brain Research|August 30, 1991
Demonstration of a novel neurofilament associated antigen with the neurofibrillary pathology of Alzheimer and related diseasesJ Gheuens, P Cras, G Perry, et al.
Revue Neurologique|June 20, 2002
[Hereditary neuropathy with liability to pressure palsies: study of six Spanish families]A Pou Serradell, J Monells, M J Téllez, et al.
Pageof 10