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Digestive Diseases and Sciences|September 18, 1999
Mitochondrial disease and cyclic vomiting syndromeR G Boles, J C Williams
Journal of Inherited Metabolic Disease|September 14, 2002
Very long-chain acyl-CoA dehydrogenase deficiency in an infant presenting with massive hepatomegalyR G Boles
Clinical Chemistry|August 3, 1999
Detection of mitochondrial DNA mutations by temporal temperature gradient gel electrophoresisT J Chen, R G Boles, L J Wong
Clinical Dysmorphology|July 1, 1994
Further delineation of the ear, patella, short stature syndrome (Meier-Gorlin syndrome)R G Boles, A S Teebi, D Schwartz, et al.
Archives of Disease in Childhood|January 15, 2008
Reflex sympathetic dystrophy: complex regional pain syndrome type I in children with mitochondrial disease and maternal inheritanceT Higashimoto, E E Baldwin, J I Gold, et al.
Human Pathology|August 1, 1994
Biochemical diagnosis of fatty acid oxidation disorders by metabolite analysis of postmortem liverR G Boles, S K Martin, M G Blitzer, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 1, 1983
Specific high-affinity binding sites for [3H]Ro 5-4864 in rat brain and kidneyH Schoemaker, R G Boles, W D Horst, et al.
The Journal of Pharmacology and Experimental Therapeutics|May 1, 1984
Temperature-dependent modulation of [3H]nitrendipine binding by the calcium channel antagonists verapamil and diltiazem in rat brain synaptosomesR G Boles, H I Yamamura, H Schoemaker, et al.
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