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C Depienne

Showing results (21-30 of 37) with videos related to

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Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: spastic paraparesis. Accession #Hs0515C Depienne, C Tallaksen, J Y Lephay, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0556C Depienne, C Tallaksen, J Y Lephay, et al.
BMJ Case Reports|June 21, 2011
Autism, language delay and mental retardation in a patient with 7q11 duplicationC Depienne, D Heron, C Betancur, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST (SPG4). Disease: Spastic paraparesis. Accession #Hm0552C Depienne, C Tallaksen, J Y Lephay, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0553C Depienne, C Tallaksen, J Y Lephay, et al.
Journal of Medical Genetics|April 3, 2007
Autism, language delay and mental retardation in a patient with 7q11 duplicationC Depienne, D Heron, C Betancur, et al.
Neurology|January 13, 2006
SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 yearsM Namekawa, P Ribai, I Nelson, et al.
Neurology|June 16, 2010
Familial cortical myoclonic tremor with epilepsy: the third locus (FCMTE3) maps to 5pC Depienne, E Magnin, D Bouteiller, et al.
European Journal of Neurology|July 14, 2012
Novel SPG10 mutation associated with dysautonomia, spinal cord atrophy, and skin biopsy abnormalityN Collongues, C Depienne, N Boehm, et al.
Neurology|April 1, 2009
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutationsK Vahedi, C Depienne, D Le Fort, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: spastic paraparesis. Accession #Hs0515C Depienne, C Tallaksen, J Y Lephay, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0556C Depienne, C Tallaksen, J Y Lephay, et al.
BMJ Case Reports|June 21, 2011
Autism, language delay and mental retardation in a patient with 7q11 duplicationC Depienne, D Heron, C Betancur, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST (SPG4). Disease: Spastic paraparesis. Accession #Hm0552C Depienne, C Tallaksen, J Y Lephay, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0553C Depienne, C Tallaksen, J Y Lephay, et al.
Journal of Medical Genetics|April 3, 2007
Autism, language delay and mental retardation in a patient with 7q11 duplicationC Depienne, D Heron, C Betancur, et al.
Neurology|January 13, 2006
SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 yearsM Namekawa, P Ribai, I Nelson, et al.
Neurology|June 16, 2010
Familial cortical myoclonic tremor with epilepsy: the third locus (FCMTE3) maps to 5pC Depienne, E Magnin, D Bouteiller, et al.
European Journal of Neurology|July 14, 2012
Novel SPG10 mutation associated with dysautonomia, spinal cord atrophy, and skin biopsy abnormalityN Collongues, C Depienne, N Boehm, et al.
Neurology|April 1, 2009
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutationsK Vahedi, C Depienne, D Le Fort, et al.
Pageof 4