Heterogeneity of phenotype in two cystic fibrosis patients homozygous for the CFTR exon 11 mutation G551D.

Por Parad, R B
Publicado em 1996

Type I C1 inhibitor deficiency with a small messenger RNA resulting from deletion of one exon.

Por Ariga, T, Igarashi, T, Ramesh, N, Parad, R, Cicardi, M, Davis, A E
Publicado em 1989

Dysfunctional C1 inhibitor Ta: deletion of Lys-251 results in acquisition of an N-glycosylation site.

Por Parad, R B, Kramer, J, Strunk, R C, Rosen, F S, Davis, A E
Publicado em 1990

Individualized developmental care for a large sample of very preterm infants: health, neurobehaviour and neurophysiology

Por McAnulty, G, Duffy, FH, Butler, S, Parad, R, Ringer, S, Zurakowski, D, Als, H
Publicado em 2009

NIDCAP improves brain function and structure in preterm infants with severe intrauterine growth restriction

Por Als, H, Duffy, F H, McAnulty, G, Butler, S C, Lightbody, L, Kosta, S, Weisenfeld, N I, Robertson, R, Parad, R B, Ringer, S A, Blickman, J G, Zurakowski, D, Warfield, S K
Publicado em 2012