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PreviewIssue DateTitleAuthor(s)
1995Longitudinal study of lipoprotein (a) in peripubertal children with insulin dependent diabetesCouper, J.; Cocciolone, R.; Bates, D.; Nairn, J.; Ryall, R.
2005Longitudinal study of normal hip development by ultrasoundRiad, J.; Cundy, P.; Gent, R.; Piotto, L.; Morris, L.; Hirte, C.
2007Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic regionFroyen, G.; Bauters, M.; Boyle, J.; Van Esch, H.; van Bokhoven, H.; Ropers, H.; Moraine, C.; Chelly, J.; Fryns, J.; Marynen, P.; Gecz, J.; Turner, G.
2010Lost in transit: the journey of ingestible temperature sensors through the human digestive tractRoach, G.D.; Sargent, C.; Darwent, D.; Kennaway, D.J.; Ferguson, S.A.
2006Lost in translation: translational interference from a recurrent mutation in exon 1 of MECP2Saxena, A.; de Lagarde, D.; Leonard, H.; Williamson, S.; Vasudevan, V.; Christodoulou, J.; Thompson, E.; MacLeod, P.; Ravine, D.
2020Low allergen content of commercial baby foodsNetting, M.J.; Gold, M.S.; Palmer, D.J.
1999Lower esophageal sphincter position in premature infants cannot be correctly estimated with current formulasOmari, T.; Benninga, M.; Haslam, R.; Barnett, C.; Davidson, G.; Dent, J.
2013Lower-limb amputee rehabilitation in Australia: analysis of a national data set 2004-10Hordacre, B.; Stevermuer, T.; Simmonds, F.; Crotty, M.; Eagar, K.
2010LPIN1 gene mutations: A major cause of severe rhabdomyolysis in early childhoodMichot, C.; Hubert, L.; Brivet, M.; De Meirleir, L.; Valayannopoulos, V.; Muller-Felber, W.; Venkateswaran, R.; Ogier, H.; Desguerre, I.; Altuzarra, C.; Thompson, E.; Smitka, M.; Huebner, A.; Husson, M.; Horvath, R.; Chinnery, P.; Vaz, F.; Munnich, A.; Elpeleg, O.; Delahodde, A.; et al.
2003Lumbar 5 ventral root transection-induced upregulation of nerve growth factor in sensory neurons and their target tissues: a mechanism in neuropathic painLi, L.; Xian, C.; Zhong, J.; Zhou, X.
2011Lung disease associated with periventricular nodular heterotopia and an FLNA mutationMasurel-Paulet, A.; Haan, E.; Thompson, E.; Goizet, C.; Thauvin-Robinet, C.; Tai, A.; Kennedy, J.; Smith, G.; Khong, T.; Sole, G.; Guerineau, E.; Coupry, I.; Huet, F.; Robertson, S.; Faivre, L.
1999Lung function outcome in children of premature birth [Review]Kennedy, J.
2004Lymphatic sparing, laparoscopic varicocelectomy: a new surgical techniqueTan, Hock Lim; Tecson, B.; Ee, M. Z.; Tantoco, J.
2010Lymphocytic bronchiolitis is associated with inadequate suppression of blood T-cell granzyme B, IFN-γ, and TNF-αHodge, G.; Hodge, S.; Liew, C.; Chambers, D.; Hopkins, P.; Reynolds, P.; Holmes, M.
2013Lynch syndrome-associated breast cancers do not overexpress chromosome 11-encoded mucinsWalsh, M.; Cummings, M.; Pearson, S.; Clendenning, M.; Walters, R.; Nagler, B.; Hopper, J.; Jenkins, M.; Suthers, G.; Goldblatt, J.; Tucker, K.; Gattas, M.; Arnold, J.; Parry, S.; Macrae, F.; McGuckin, M.; Young, J.; Buchanan, D.
2010Lynch syndrome-associated breast cancers: Clinicopathologic characteristics of a case series from the colon cancer family registryWalsh, M.; Buchanan, D.; Cummings, M.; Pearson, S.; Arnold, S.; Clendenning, M.; Walters, R.; McKeone, D.; Spurdle, A.; Hopper, J.; Jenkins, M.; Phillips, K.; Suthers, G.; George, J.; Goldblatt, J.; Muir, A.; Tucker, K.; Pelzer, E.; Gattas, M.; Woodall, S.; et al.
2010Lysophosphatidylcholine as an adjuvant for lentiviral vector mediated gene transfer to airway epithelium: effect of acyl chain lengthCmielewski, P.; Anson, D.; Parsons, D.
1997Lysosomal biogenesis in lysosomal storage disordersKarageorgos, L.; Isaac, E.; Brooks, D.; Ravenscroft, E.; Davey, R.; Hopwood, J.; Meikle, P.
2012Lysosomal secretion of Flightless I upon injury has the potential to alter inflammationCowin, A.; Lei, N.; Franken, L.; Ruzehaji, N.; Offenhauser, C.; Kopecki, Z.; Murray, R.
2003Lysosomal storage disorders: emerging therapeutic options require early diagnosisMeikle, P.; Hopwood, J.