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S L Rutledge

Showing results (11-20 of 20) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1995
3-Hydroxyisovalerylcarnitine in 3-methylcrotonyl-CoA carboxylase deficiencyJ L van Hove, S L Rutledge, M A Nada, et al.
Neurology|October 22, 1998
Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotypeC S Benton, R de Silva, S L Rutledge, et al.
The Journal of Pediatrics|January 1, 1990
Neonatal hemodialysis: effective therapy for the encephalopathy of inborn errors of metabolismS L Rutledge, P L Havens, M W Haymond, et al.
Progress in Clinical and Biological Research|January 1, 1992
Molecular characterization of medium-chain acyl-CoA dehydrogenase deficiency causing sudden deathD P Kelly, A J Whelan, D E Hale, et al.
Neurology|February 19, 2000
Acute hydrocephalus in nonketotic hyperglycinemiaJ L Van Hove, P S Kishnani, P Demaerel, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Molecular basis of inherited medium-chain acyl-CoA dehydrogenase deficiency causing sudden child deathD P Kelly, D E Hale, S L Rutledge, et al.
Pediatric Neurology|July 1, 1989
Pyruvate carboxylase deficiency: acute exacerbation after ACTH treatment of infantile spasmsS L Rutledge, O C Snead, D R Kelly, et al.
Nature Genetics|May 1, 1995
Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3pL G Gouw, C D Kaplan, J H Haines, et al.
American Journal of Human Genetics|June 15, 2007
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiencyM He, S L Rutledge, D R Kelly, et al.
Pediatric Research|November 1, 1990
Heteroplasmy in chronic external ophthalmoplegia: clinical and molecular observationsO Hurko, D R Johns, S L Rutledge, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Journal of Inherited Metabolic Disease|January 1, 1995
3-Hydroxyisovalerylcarnitine in 3-methylcrotonyl-CoA carboxylase deficiencyJ L van Hove, S L Rutledge, M A Nada, et al.
Neurology|October 22, 1998
Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotypeC S Benton, R de Silva, S L Rutledge, et al.
The Journal of Pediatrics|January 1, 1990
Neonatal hemodialysis: effective therapy for the encephalopathy of inborn errors of metabolismS L Rutledge, P L Havens, M W Haymond, et al.
Progress in Clinical and Biological Research|January 1, 1992
Molecular characterization of medium-chain acyl-CoA dehydrogenase deficiency causing sudden deathD P Kelly, A J Whelan, D E Hale, et al.
Neurology|February 19, 2000
Acute hydrocephalus in nonketotic hyperglycinemiaJ L Van Hove, P S Kishnani, P Demaerel, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Molecular basis of inherited medium-chain acyl-CoA dehydrogenase deficiency causing sudden child deathD P Kelly, D E Hale, S L Rutledge, et al.
Pediatric Neurology|July 1, 1989
Pyruvate carboxylase deficiency: acute exacerbation after ACTH treatment of infantile spasmsS L Rutledge, O C Snead, D R Kelly, et al.
Nature Genetics|May 1, 1995
Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3pL G Gouw, C D Kaplan, J H Haines, et al.
American Journal of Human Genetics|June 15, 2007
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiencyM He, S L Rutledge, D R Kelly, et al.
Pediatric Research|November 1, 1990
Heteroplasmy in chronic external ophthalmoplegia: clinical and molecular observationsO Hurko, D R Johns, S L Rutledge, et al.
Pageof 2