Infant

Acyl-CoA Dehydrogenase

Genotype-phenotype correlations: sudden death in an infant with very-long-chain acyl-CoA dehydrogenase deficiency

Curtis R. Coughlin

• Dec 1, 2010 • 1 min read

Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease

Matthew G. Sampson

• Oct 1, 2010 • 1 min read

Acyl-CoA Dehydrogenase

Very long-chain acyl-CoA dehydrogenase deficiency in a patient with normal newborn screening by tandem mass spectrometry

Can Ficicioglu

• Mar 1, 2010 • 1 min read

Child neurology: a case illustrating the role of imaging in evaluation of sudden infant death

Sarah M. Kranick

• Sep 1, 2009 • 1 min read

Penicillamine therapy for pediatric cystinuria: experience from a cohort of American children

Ralph J. DeBerardinis

• Dec 1, 2008 • 1 min read