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C Ceuterick

Showing results (61-70 of 92) with videos related to

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The American Journal of Pathology|July 1, 1994
Microtubule-associated protein tau epitopes are present in fiber lesions in diverse muscle disordersU Lübke, J Six, M Villanova, et al.
Acta Neuropathologica|January 1, 1992
Specific monoclonal antibodies against normal microtubule-associated protein-2 (MAP2) epitopes present in Alzheimer pathological structures do not recognize paired helical filamentsJ Six, U Lübke, M Mercken, et al.
Archives of Neurology|August 2, 2001
A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndromeS Seneca, H Verhelst, L De Meirleir, et al.
Clinical Neurology and Neurosurgery|January 1, 1992
Becker-type muscular dystrophy. Report of a family with one postmortem studyJ J Martin, J Leroy, C Ceuterick, et al.
Acta Neurologica Scandinavica|April 1, 1999
Infantile and juvenile presentations of Alexander's disease: a report of two casesM Deprez, M D'Hooghe, J P Misson, et al.
Acta Neurologica Belgica|September 23, 2018
Early-onset dementia, leukoencephalopathy and brain calcifications: a clinical, imaging and pathological comparison of ALSP and PLOSL/Nasu Hakola diseaseC Coomans, A Sieben, M Lammens, et al.
Journal of the Neurological Sciences|May 1, 1992
Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigreeV Timmerman, P Raeymaekers, E Nelis, et al.
Neuropediatrics|November 1, 1986
Benign mitochondrial myopathy with deficiency of NADH-CoQ reductase and cytochrome c oxidaseA M Roodhooft, K J Van Acker, J J Martin, et al.
Clinical Neuropathology|July 1, 1993
Eosinophilia-myalgia syndrome: a clinicopathological study of four patientsM Villanova, L S De Clerck, P Cras, et al.
Neuromuscular Disorders : NMD|May 23, 2001
A novel 3'-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsiesJ Meuleman, A Pou-Serradell, A Löfgren, et al.
Pageof 10

Showing results (61-70 of 92) with videos related to

Sort By:
Pageof 10
The American Journal of Pathology|July 1, 1994
Microtubule-associated protein tau epitopes are present in fiber lesions in diverse muscle disordersU Lübke, J Six, M Villanova, et al.
Acta Neuropathologica|January 1, 1992
Specific monoclonal antibodies against normal microtubule-associated protein-2 (MAP2) epitopes present in Alzheimer pathological structures do not recognize paired helical filamentsJ Six, U Lübke, M Mercken, et al.
Archives of Neurology|August 2, 2001
A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndromeS Seneca, H Verhelst, L De Meirleir, et al.
Clinical Neurology and Neurosurgery|January 1, 1992
Becker-type muscular dystrophy. Report of a family with one postmortem studyJ J Martin, J Leroy, C Ceuterick, et al.
Acta Neurologica Scandinavica|April 1, 1999
Infantile and juvenile presentations of Alexander's disease: a report of two casesM Deprez, M D'Hooghe, J P Misson, et al.
Acta Neurologica Belgica|September 23, 2018
Early-onset dementia, leukoencephalopathy and brain calcifications: a clinical, imaging and pathological comparison of ALSP and PLOSL/Nasu Hakola diseaseC Coomans, A Sieben, M Lammens, et al.
Journal of the Neurological Sciences|May 1, 1992
Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigreeV Timmerman, P Raeymaekers, E Nelis, et al.
Neuropediatrics|November 1, 1986
Benign mitochondrial myopathy with deficiency of NADH-CoQ reductase and cytochrome c oxidaseA M Roodhooft, K J Van Acker, J J Martin, et al.
Clinical Neuropathology|July 1, 1993
Eosinophilia-myalgia syndrome: a clinicopathological study of four patientsM Villanova, L S De Clerck, P Cras, et al.
Neuromuscular Disorders : NMD|May 23, 2001
A novel 3'-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsiesJ Meuleman, A Pou-Serradell, A Löfgren, et al.
Pageof 10