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C Ceuterick

Showing results (81-90 of 92) with videos related to

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Acta Neuropathologica|January 1, 1994
On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one familyJ J Martin, N Van Regemorter, L Krols, et al.
European Neurology|February 25, 2000
Type I sialidosis: a clinical, biochemical and neuroradiological studyS Palmeri, M Villanova, A Malandrini, et al.
Neurology|June 17, 1999
Novel missense mutation in the early growth response 2 gene associated with Dejerine-Sottas syndrome phenotypeV Timmerman, P De Jonghe, C Ceuterick, et al.
Acta Neuropathologica|July 21, 1999
Detection of beta-A4 amyloid and its precursor protein in the muscle of a patient with juvenile neuronal ceroid lipofuscinosis (Spielmeyer-Vogt-Sjögren)M Villanova, C Ceuterick, M T Dotti, et al.
Brain : a Journal of Neurology|March 10, 1999
The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotypeP De Jonghe, V Timmerman, C Ceuterick, et al.
Acta Neuropathologica|October 1, 1998
Presenile Alzheimer dementia characterized by amyloid angiopathy and large amyloid core type senile plaques in the APP 692Ala-->Gly mutationP Cras, F van Harskamp, L Hendriks, et al.
Neurology|February 9, 2005
Myosin storage myopathy: slow skeletal myosin (MYH7) mutation in two isolated casesN G Laing, C Ceuterick-de Groote, D E Dye, et al.
Neurobiology of Disease|February 15, 2000
Behavioral disturbances without amyloid deposits in mice overexpressing human amyloid precursor protein with Flemish (A692G) or Dutch (E693Q) mutationS Kumar-Singh, I Dewachter, D Moechars, et al.
Neuromuscular Disorders : NMD|February 5, 2003
Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegiaG Van Goethem, J J Martin, B Dermaut, et al.
Neurology|December 25, 2002
Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathyE Nelis, S Erdem, P Y K Van Den Bergh, et al.
Pageof 10

Showing results (81-90 of 92) with videos related to

Sort By:
Pageof 10
Acta Neuropathologica|January 1, 1994
On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one familyJ J Martin, N Van Regemorter, L Krols, et al.
European Neurology|February 25, 2000
Type I sialidosis: a clinical, biochemical and neuroradiological studyS Palmeri, M Villanova, A Malandrini, et al.
Neurology|June 17, 1999
Novel missense mutation in the early growth response 2 gene associated with Dejerine-Sottas syndrome phenotypeV Timmerman, P De Jonghe, C Ceuterick, et al.
Acta Neuropathologica|July 21, 1999
Detection of beta-A4 amyloid and its precursor protein in the muscle of a patient with juvenile neuronal ceroid lipofuscinosis (Spielmeyer-Vogt-Sjögren)M Villanova, C Ceuterick, M T Dotti, et al.
Brain : a Journal of Neurology|March 10, 1999
The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotypeP De Jonghe, V Timmerman, C Ceuterick, et al.
Acta Neuropathologica|October 1, 1998
Presenile Alzheimer dementia characterized by amyloid angiopathy and large amyloid core type senile plaques in the APP 692Ala-->Gly mutationP Cras, F van Harskamp, L Hendriks, et al.
Neurology|February 9, 2005
Myosin storage myopathy: slow skeletal myosin (MYH7) mutation in two isolated casesN G Laing, C Ceuterick-de Groote, D E Dye, et al.
Neurobiology of Disease|February 15, 2000
Behavioral disturbances without amyloid deposits in mice overexpressing human amyloid precursor protein with Flemish (A692G) or Dutch (E693Q) mutationS Kumar-Singh, I Dewachter, D Moechars, et al.
Neuromuscular Disorders : NMD|February 5, 2003
Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegiaG Van Goethem, J J Martin, B Dermaut, et al.
Neurology|December 25, 2002
Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathyE Nelis, S Erdem, P Y K Van Den Bergh, et al.
Pageof 10