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Results 61-70 of 255 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2002Economic inequality, working-class power, social capital, and cause-specific mortality in wealthy countriesMuntaner, C.; Lynch, J.W.; Hillemeier, M.; Lee, J.H.; David, R.; Benach, J.; Borrell, C.
2009Prevalence of refractive errors in a Brazilian population: the Botucatu Eye StudySchellini, S.; Durkin, S.; Hoyama, E.; Hirai, F.; Cordeiro, R.; Casson, R.; Selva, D.; Padovani, C.
2001Relationship between straining, transient lower esophageal sphincter relaxation, and gastroesophageal reflux in childrenKawahara, H.; Dent, J.; Davidson, G.; Okada, A.
2000Fourier analysis of facial profiles of young twinsTangchaitrong, K.; Messer, L.; Thomas, C.; Townsend, G.
2008Antibody-mediated growth inhibition of Plasmodium falciparum: Relationship to age and protection from parasitemia in Kenyan children and adultsDent, A.; Bergmann-Leitner, E.; Wilson, D.; Tisch, D.; Kimmel, R.; Vulule, J.; Sumba, P.; Beeson, J.; Angov, E.; Moormann, A.; Kazura, J.; Sutherland, C.J.
2004Benign familial neonatal-infantile seizures: Characterization of a new sodium channelopathyBerkovic, S.; Heron, S.; Giordano, L.; Marini, C.; Guerrini, R.; Kaplan, R.; Gambardella, A.; Steinlein, O.; Grinton, B.; Dean, J.; Bordo, L.; Hodgson, B.; Yamamoto, T.; Mulley, J.; Zara, F.; Scheffer, I.
2005Threshold effect of urinary glycosaminoglycans and the walk test as indicators of disease progression in a survey of subjects with mucopolysaccharidosis VI (Maroteaux-Lamy syndrome)Swiedler, S.; Beck, M.; Bajbouj, M.; Giugliani, R.; Schwartz, I.; Harmatz, P.; Wraith, J.; Roberts, J.; Ketteridge, D.; Hopwood, J.; Guffon, N.; Miranda, C.; Teles, E.; Berger, K.; Piscia-Nichols, C.
2006Hepatocellular carcinoma in ten children under five years of age with bile salt export pump deficiencyKnisely, A.; Strautnieks, S.; Meier, Y.; Stieger, B.; Byrne, J.; Portmann, B.; Bull, L.; Pawlikowska, L.; Bilezikci, B.; Ozcay, F.; Laszlo, A.; Tiszlavicz, L.; Moore, L.; Raftos, J.; Arnell, H.; Fischler, B.; Nemeth, A.; Papadogiannakis, N.; Cielecka-Kuszyk, J.; Jankowska, I.; et al.
2003X-linked mild non-syndromic mental retardation with neuropsychiatric problems and the missense mutation A365E in PAK3Gedeon, A.; Nelson, J.; Gecz, J.; Mulley, J.
2004Twenty-two novel mutations in the lysosomal a-glucosidase gene (GAA) underscore the genotype-phenotype correlation in glycogen storage disease type IIHermans, M.; van Leenen, D.; Kroos, M.; Beesley, C.; Van der Ploeg, A.; Sakuraba, H.; Wevers, R.; Kleijer, W.; Mikelakakis, H.; Kirk, E.; Fletcher, J.; Bosshard, N.; Basel-Vanagaite, L.; Besley, G.; Reuser, A.