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Journal of Inherited Metabolic Disease|October 13, 1999
Urinary organic acid screening in children with developmental language delayM Michelson, S Harel, A Gutman, et al.Journal of Child Neurology|August 29, 2000
Methylenetetrahydrofolate reductase deficiency: importance of early diagnosisA Fattal-Valevski, H Bassan, S H Korman, et al.Harefuah|June 15, 1995
[Epidemiology of developmental disorders in children in Tel Aviv]E Samuel, T Lerman-Sagie, Y Nevo, et al.Archives of Disease in Childhood|August 18, 1999
Multiple presentation of mitochondrial disordersA Nissenkorn, A Zeharia, D Lev, et al.Neurology|June 1, 2001
Inborn errors of metabolism: a cause of abnormal brain developmentA Nissenkorn, M Michelson, B Ben-Zeev, et al.Journal of Child Neurology|January 21, 2000
Neurologic presentations of mitochondrial disordersA Nissenkorn, A Zeharia, D Lev, et al.Harefuah|September 1, 1996
[Bilateral operculum syndrome]T Lerman-Sagie, E Porat-Alkabetz, J J Meir, et al.American Journal of Medical Genetics|May 16, 1997
Heterogeneity in adducted thumbs sequenceM Moldavsky, T Lerman-Sagie, M Kutai, et al.Journal of Child Neurology|June 27, 2000
Familial mitochondrial intestinal pseudo-obstruction and neurogenic bladderL T Haftel, D Lev, V Barash, et al.Pageof 80