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M I Shevell

Showing results (61-70 of 69) with videos related to

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Neurology|September 30, 2011
Evidence report: Genetic and metabolic testing on children with global developmental delay [RETIRED]: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology SocietyD J Michelson, M I Shevell, E H Sherr, et al.
Journal of Inherited Metabolic Disease|August 1, 1997
Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC)D S Rosenblatt, A L Aspler, M I Shevell, et al.
American Journal of Medical Genetics|December 18, 1995
Adenylosuccinate lyase (ADSL) and infantile autism: absence of previously reported point mutationE A Fon, J Sarrazin, C Meunier, et al.
Neurology|February 8, 2012
So what? Does the test lead to improved health outcomes?D J Michelson, M I Shevell, E H Sherr, et al.
Pediatric Neurology|May 2, 2000
Neuronal dysfunction in children with newly diagnosed temporal lobe epilepsyS P Miller, L M Li, F Cendes, et al.
Pediatric Neurology|May 1, 1994
Encephaloduroarteriosynangiosis (EDAS) for the treatment of childhood moyamoya diseaseI B Ross, M I Shevell, J L Montes, et al.
Pediatric Neurology|October 1, 1994
Cerebral dysgenesis and lactic acidemia: an MRI/MRS phenotype associated with pyruvate dehydrogenase deficiencyM I Shevell, P M Matthews, C R Scriver, et al.
Brain Pathology (Zurich, Switzerland)|October 1, 1993
Searching for human epilepsy genes: a progress reportM Leppert, W M McMahon, T G Quattlebaum, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 5, 1998
Monoaminergic effects of high-dose corticotropin in corticotropin-responsive pediatric opsoclonus-myoclonusM R Pranzatelli, Y Y Huang, E Tate, et al.
Pageof 7

Showing results (61-70 of 69) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 69 results.
Neurology|September 30, 2011
Evidence report: Genetic and metabolic testing on children with global developmental delay [RETIRED]: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology SocietyD J Michelson, M I Shevell, E H Sherr, et al.
Journal of Inherited Metabolic Disease|August 1, 1997
Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC)D S Rosenblatt, A L Aspler, M I Shevell, et al.
American Journal of Medical Genetics|December 18, 1995
Adenylosuccinate lyase (ADSL) and infantile autism: absence of previously reported point mutationE A Fon, J Sarrazin, C Meunier, et al.
Neurology|February 8, 2012
So what? Does the test lead to improved health outcomes?D J Michelson, M I Shevell, E H Sherr, et al.
Pediatric Neurology|May 2, 2000
Neuronal dysfunction in children with newly diagnosed temporal lobe epilepsyS P Miller, L M Li, F Cendes, et al.
Pediatric Neurology|May 1, 1994
Encephaloduroarteriosynangiosis (EDAS) for the treatment of childhood moyamoya diseaseI B Ross, M I Shevell, J L Montes, et al.
Pediatric Neurology|October 1, 1994
Cerebral dysgenesis and lactic acidemia: an MRI/MRS phenotype associated with pyruvate dehydrogenase deficiencyM I Shevell, P M Matthews, C R Scriver, et al.
Brain Pathology (Zurich, Switzerland)|October 1, 1993
Searching for human epilepsy genes: a progress reportM Leppert, W M McMahon, T G Quattlebaum, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 5, 1998
Monoaminergic effects of high-dose corticotropin in corticotropin-responsive pediatric opsoclonus-myoclonusM R Pranzatelli, Y Y Huang, E Tate, et al.
Pageof 7