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G Ponsot

Showing results (111-120 of 156) with videos related to

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Archives Francaises De Pediatrie|November 1, 1983
[Nosological aspects of epilepsia partialis continua in children]O Dulac, C Dravet, P Plouin, et al.
Journal of Inherited Metabolic Disease|November 20, 1998
Diffuse leukodystrophy in an infant with cytochrome-c oxidase deficiencyJ P Harpey, D Heron, M Prudent, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 10, 2001
[Cerebellar vermis hypoplasia with extracerebral involvement (retina, kidney, liver): difficult to classify syndromes]D Graber, C Antignac, G Deschenes, et al.
Biochemical and Biophysical Research Communications|March 7, 1996
Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory chainM A Birch-Machin, C Marsac, G Ponsot, et al.
American Journal of Medical Genetics|March 1, 1992
Segregation of three reciprocal translocations in the same family: t(3;4), t(5;10), and t(15;21)L Telvi, M Folhen, O Raoul, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 16, 2006
[Fetal neurology: conditions of diagnostic uncertainty]M-L Moutard, A Gélot, D Rodriguez, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
A near homoplasmic T8993G mtDNA mutation in a patient with atypic Leigh syndrome not present in the mother's tissuesF Degoul, D François, M Diry, et al.
Journal of the Peripheral Nervous System : JPNS|August 26, 2000
Congenital insensitivity to pain with anhydrosis. Report of two unrelated casesA Vital, D Fontan, J Julien, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1988
Peripheral neuropathy associated with erythrophagocytic lymphohistiocytosisB Boutin, M C Routon, F Rocchiccioli, et al.
Neuropediatrics|November 5, 2003
Infantile spasms with basal ganglia MRI hypersignal may reveal mitochondrial disorder due to T8993G MT DNA mutationI Desguerre, F Pinton, R Nabbout, et al.
Pageof 16

Showing results (111-120 of 156) with videos related to

Sort By:
Pageof 16
Archives Francaises De Pediatrie|November 1, 1983
[Nosological aspects of epilepsia partialis continua in children]O Dulac, C Dravet, P Plouin, et al.
Journal of Inherited Metabolic Disease|November 20, 1998
Diffuse leukodystrophy in an infant with cytochrome-c oxidase deficiencyJ P Harpey, D Heron, M Prudent, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 10, 2001
[Cerebellar vermis hypoplasia with extracerebral involvement (retina, kidney, liver): difficult to classify syndromes]D Graber, C Antignac, G Deschenes, et al.
Biochemical and Biophysical Research Communications|March 7, 1996
Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory chainM A Birch-Machin, C Marsac, G Ponsot, et al.
American Journal of Medical Genetics|March 1, 1992
Segregation of three reciprocal translocations in the same family: t(3;4), t(5;10), and t(15;21)L Telvi, M Folhen, O Raoul, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 16, 2006
[Fetal neurology: conditions of diagnostic uncertainty]M-L Moutard, A Gélot, D Rodriguez, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
A near homoplasmic T8993G mtDNA mutation in a patient with atypic Leigh syndrome not present in the mother's tissuesF Degoul, D François, M Diry, et al.
Journal of the Peripheral Nervous System : JPNS|August 26, 2000
Congenital insensitivity to pain with anhydrosis. Report of two unrelated casesA Vital, D Fontan, J Julien, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1988
Peripheral neuropathy associated with erythrophagocytic lymphohistiocytosisB Boutin, M C Routon, F Rocchiccioli, et al.
Neuropediatrics|November 5, 2003
Infantile spasms with basal ganglia MRI hypersignal may reveal mitochondrial disorder due to T8993G MT DNA mutationI Desguerre, F Pinton, R Nabbout, et al.
Pageof 16