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Evidence report: Genetic and metabolic testing on children with global developmental delay: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.
A monoclonal antibody to O-acetyl-GD2 ganglioside and not to GD2 shows potent anti-tumor activity without peripheral nervous system cross-reactivity.
Cardiovascular pharmacogenomics.
GFAP mutations, age at onset, and clinical subtypes in Alexander disease.
Donor myocardial infarction impairs the therapeutic potential of bone marrow cells by an interleukin-1-mediated inflammatory response.
Laterality of brain and ocular lesions in Aicardi syndrome.
Iroquois homeobox gene 3 establishes fast conduction in the cardiac His-Purkinje network.
Treatment of vitamin D deficiency in transfusion-dependent thalassemia.
Atrial natriuretic factor in the developing heart: a signpost for cardiac morphogenesis.
Ezh2 regulates anteroposterior axis specification and proximodistal axis elongation in the developing limb.