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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 the Child Neurology Society|August 7, 2026
Early neurodevelopmental follow-up results from the NEOLEV2 cohortCynthia Sharpe, Gail E Reiner, Peter W Reed, et al.European Journal of Immunology|March 26, 1999
Dietary lectins can induce in vitro release of IL-4 and IL-13 from human basophilsH Haas, F H Falcone, G Schramm, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 3, 2011
Quality improvement of mitochondrial respiratory chain complex enzyme assays using Caenorhabditis elegansXiulian Chen, David R Thorburn, Lee-Jun Wong, et al.Molecular Genetics and Metabolism|February 5, 2008
The in-depth evaluation of suspected mitochondrial disease, Richard H Haas, Sumit Parikh, et al.Journal of Medical Virology|January 1, 1977
Seroepidemiological investigation of patients and family contacts in an epidemic of hepatitis AG G Frösner, L R Overby, B Flehmig, 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.Optics Express|October 19, 2017
InGaN µLEDs integrated onto colloidal quantum dot functionalized ultra-thin glassK Rae, C Foucher, B Guilhabert, et al.Molecular and Biochemical Parasitology|February 17, 2006
IPSE/alpha-1: a major immunogenic component secreted from Schistosoma mansoni eggsG Schramm, A Gronow, J Knobloch, et al.Pageof 40