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Digestive Diseases and Sciences|September 18, 1999
Mitochondrial disease and cyclic vomiting syndromeR G Boles, J C WilliamsClinical Dysmorphology|May 18, 1999
Cleft palate, ptosis, digital anomalies and mental retardation: a new syndrome or a distal arthrogryposis variant?R G BolesJournal of Inherited Metabolic Disease|September 14, 2002
Very long-chain acyl-CoA dehydrogenase deficiency in an infant presenting with massive hepatomegalyR G BolesPediatric Cardiology|November 25, 2003
Severe reversible cardiomyopathy in four unrelated infants associated with mitochondrial DNA D-loop heteroplasmyR G Boles, C Luna, M ItoClinical Chemistry|August 3, 1999
Detection of mitochondrial DNA mutations by temporal temperature gradient gel electrophoresisT J Chen, R G Boles, L J WongClinical 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.Pageof 51