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R H Haas

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Muscle & Nerve|June 19, 2001
Nerve conduction changes in patients with mitochondrial diseases treated with dichloroacetateL Spruijt, R K Naviaux, K A McGowan, et al.
Pediatric Research|December 1, 1989
Cardiac function, substrate utilization, and myocardial energy metabolism studied with 31-P NMR spectroscopy during acute hypoglycemia and hyperketonemiaJ Breuer, K J Chung, E Pesonen, et al.
Journal of Child Neurology|January 1, 1995
Acute basal ganglia infarction in propionic acidemiaR H Haas, D L Marsden, S Capistrano-Estrada, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1997
Diabetes and mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS): radiolabeled polymerase chain reaction is necessary for accurate detection of low percentages of mutationM L Smith, X Y Hua, D L Marsden, et al.
Lancet (London, England)|January 1, 1994
Cerebellar hypoplasia and hyperplasia in infantile autismE Courchesne, O Saitoh, J P Townsend, 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.
Annals of Neurology|August 1, 1995
Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutationJ M Shoffner, M D Brown, C Stugard, et al.
Behavioral Neuroscience|October 1, 1994
Impairment in shifting attention in autistic and cerebellar patientsE Courchesne, J Townsend, N A Akshoomoff, et al.
Molecular Genetics and Metabolism|November 26, 2008
Expanded clinical and molecular spectrum of guanidinoacetate methyltransferase (GAMT) deficiencyS U Dhar, F Scaglia, F-Y Li, et al.
Neurology|July 27, 2001
Unusual brain growth patterns in early life in patients with autistic disorder: an MRI studyE Courchesne, C M Karns, H R Davis, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Muscle & Nerve|June 19, 2001
Nerve conduction changes in patients with mitochondrial diseases treated with dichloroacetateL Spruijt, R K Naviaux, K A McGowan, et al.
Pediatric Research|December 1, 1989
Cardiac function, substrate utilization, and myocardial energy metabolism studied with 31-P NMR spectroscopy during acute hypoglycemia and hyperketonemiaJ Breuer, K J Chung, E Pesonen, et al.
Journal of Child Neurology|January 1, 1995
Acute basal ganglia infarction in propionic acidemiaR H Haas, D L Marsden, S Capistrano-Estrada, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1997
Diabetes and mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS): radiolabeled polymerase chain reaction is necessary for accurate detection of low percentages of mutationM L Smith, X Y Hua, D L Marsden, et al.
Lancet (London, England)|January 1, 1994
Cerebellar hypoplasia and hyperplasia in infantile autismE Courchesne, O Saitoh, J P Townsend, 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.
Annals of Neurology|August 1, 1995
Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutationJ M Shoffner, M D Brown, C Stugard, et al.
Behavioral Neuroscience|October 1, 1994
Impairment in shifting attention in autistic and cerebellar patientsE Courchesne, J Townsend, N A Akshoomoff, et al.
Molecular Genetics and Metabolism|November 26, 2008
Expanded clinical and molecular spectrum of guanidinoacetate methyltransferase (GAMT) deficiencyS U Dhar, F Scaglia, F-Y Li, et al.
Neurology|July 27, 2001
Unusual brain growth patterns in early life in patients with autistic disorder: an MRI studyE Courchesne, C M Karns, H R Davis, et al.
Pageof 5