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W D Graf

Showing results (21-30 of 31) with videos related to

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Neuropediatrics|October 8, 1998
Altered antioxidant enzyme activities in children with a serious adverse experience related to valproic acid therapyW D Graf, O E Oleinik, T A Glauser, et al.
Annals of Neurology|January 13, 2000
Diffusion-weighted magnetic resonance imaging in boys with neural cell adhesion molecule L1 mutations and congenital hydrocephalusW D Graf, D E Born, D W Shaw, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|December 1, 1995
Comparison of erythrocyte antioxidant enzyme activities and embryologic level of neural tube defectsW D Graf, O E Oleinik, C E Pippenger, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|February 8, 2000
Brainstem diffusion-weighted MRI in boys with L1CAM mutationsW D Graf, D E Born, D W Shaw, et al.
Neurology|June 1, 1993
Clinical features associated with the A-->G transition at nucleotide 8344 of mtDNA ("MERRF mutation")G Silvestri, E Ciafaloni, F M Santorelli, et al.
Cancer|April 1, 1996
Severe vincristine neuropathy in Charcot-Marie-Tooth disease type 1AW D Graf, P F Chance, M W Lensch, et al.
Neurology|November 24, 1999
A placebo-controlled trial of lamotrigine add-on therapy for partial seizures in children. Lamictal Pediatric Partial Seizure Study GroupM Duchowny, J M Pellock, W D Graf, et al.
Annals of Neurology|June 1, 1993
Phenotypic heterogeneity in families with the myoclonic epilepsy and ragged-red fiber disease point mutation in mitochondrial DNAW D Graf, S M Sumi, M K Copass, et al.
Cytogenetic and Genome Research|August 19, 2011
Identification of copy number variants on human chromosome 22 in patients with a variety of clinical findingsS Yu, W D Graf, A Ramalingam, et al.
Journal of Child Neurology|June 27, 2000
Autism associated with the mitochondrial DNA G8363A transfer RNA(Lys) mutationW D Graf, J Marin-Garcia, H G Gao, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Neuropediatrics|October 8, 1998
Altered antioxidant enzyme activities in children with a serious adverse experience related to valproic acid therapyW D Graf, O E Oleinik, T A Glauser, et al.
Annals of Neurology|January 13, 2000
Diffusion-weighted magnetic resonance imaging in boys with neural cell adhesion molecule L1 mutations and congenital hydrocephalusW D Graf, D E Born, D W Shaw, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|December 1, 1995
Comparison of erythrocyte antioxidant enzyme activities and embryologic level of neural tube defectsW D Graf, O E Oleinik, C E Pippenger, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|February 8, 2000
Brainstem diffusion-weighted MRI in boys with L1CAM mutationsW D Graf, D E Born, D W Shaw, et al.
Neurology|June 1, 1993
Clinical features associated with the A-->G transition at nucleotide 8344 of mtDNA ("MERRF mutation")G Silvestri, E Ciafaloni, F M Santorelli, et al.
Cancer|April 1, 1996
Severe vincristine neuropathy in Charcot-Marie-Tooth disease type 1AW D Graf, P F Chance, M W Lensch, et al.
Neurology|November 24, 1999
A placebo-controlled trial of lamotrigine add-on therapy for partial seizures in children. Lamictal Pediatric Partial Seizure Study GroupM Duchowny, J M Pellock, W D Graf, et al.
Annals of Neurology|June 1, 1993
Phenotypic heterogeneity in families with the myoclonic epilepsy and ragged-red fiber disease point mutation in mitochondrial DNAW D Graf, S M Sumi, M K Copass, et al.
Cytogenetic and Genome Research|August 19, 2011
Identification of copy number variants on human chromosome 22 in patients with a variety of clinical findingsS Yu, W D Graf, A Ramalingam, et al.
Journal of Child Neurology|June 27, 2000
Autism associated with the mitochondrial DNA G8363A transfer RNA(Lys) mutationW D Graf, J Marin-Garcia, H G Gao, et al.
Pageof 4