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20041024C>T (R342X) is a recurrent RHF6 mutation also found in the original Börjeson-Forssman-Lehmann syndrome familyLower, K.; Solders, G.; Bondeson, M.; Nelson, J.; Brun, A.; Crawford, J.; Malm, G.; Borjeson, M.; Turner, G.; Partington, M.; Gecz, J.
20101210 Methodological approaches to conceptualizing and modeling the effect of dynamic family structure on child behaviorMcDonald, S.; Moodie, E.; Lynch, J.; Satellite Symposia
201214q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elementsAllou, L.; Lambert, L.; Amsallem, D.; Bieth, E.; Edery, P.; Destree, A.; Rivier, F.; Amor, D.; Thompson, E.; Nicholl, J.; Harbord, M.; Nemos, C.; Saunier, A.; Moustaine, A.; Vigouroux, A.; Jonveaux, P.; Philippe, C.
201117-alpha-hydroxyprogesterone caproate for the prevention of adverse neonatal outcome in multiple pregnancies: A randomized controlled trialLim, A.; Schuit, E.; Bloemenkamp, K.; Bernardus, R.; Duvekot, J.; Erwich, J.; van Eyck, J.; Groenwold, R.; Hasaart, T.; Hummel, P.; Kars, M.; Kwee, A.; van Oirschot, C.; van Pampus, M.; Papatsonis, D.; Porath, M.; Spaanderman, M.; Willekes, C.; Wilpshaar, J.; Mol, B.; et al.
20081D09C3, an mAb specific for MHC-IIZola, H.; Beare, A.
2015236 effect of cyclic adenosine monophosphate modulator regulators in association with bmp15 on bovine embryo development in vitroMachado, M.F.; Nogueira, M.F.; Gilchrist, R.B.; Sutton-McDowall, M.L.; Mottershead, D.G.; White, M.A.; Thompson, J.G.; : Australia)
201425-hydroxyvitamin D concentrations in children with Crohn's disease supplemented with either 2000 or 400 IU daily for 6 months: a randomized controlled studyWingate, K.; Jacobson, K.; Issenman, R.; Carroll, M.; Barker, C.; Israel, D.; Brill, H.; Weiler, H.; Barr, S.; Li, W.; Lyon, M.; Green, T.
20114-aminobutyrate aminotrasferase (ABAT): genetic and pharmacological evidence for an involvement in gastro esophageal reflux diseaseJirholt, J.; Asling, B.; Hammond, P.; Davidson, G.; Knutsson, M.; Walentinsson, A.; Jensen, J.; Lehmann, A.; Agreus, L.; Lagerstrom-Fermer, M.
2009A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technologyTalseth-Palmer, B.; Bowden, N.; Meldrum, C.; Nicholl, J.; Thompson, E.; Friend, K.; Liebelt, J.; Bratkovic, D.; Haan, E.; Yu, S.; Scott, R.
1996A 3-year follow-up of the intellectual and academic functioning of children receiving central nervous system prophylactic chemotherapy for leukemiaBrown, R.; Sawyer, M.; Antoniou, G.; Toogood, I.; Rice, M.; Thompson, N.; Madan-Swain, A.
2012A bivalent Neisserie meningitidis recombinant lipidated factor H binding protein vaccine in young adults: results of a randomised, controlled, dose-escalation phase 1 trialRichmond, P.; Nissen, M.; Marshall, H.; Lambert, S.; Roberton, D.; Gruber, W.; Jones, T.; Arora, A.
2018A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriersZhang, M.; Ferrari, R.; Tartaglia, M.C.; Keith, J.; Surace, E.I.; Wolf, U.; Sato, C.; Grinberg, M.; Liang, Y.; Xi, Z.; Dupont, K.; McGoldrick, P.; Weichert, A.; McKeever, P.M.; Schneider, R.; McCorkindale, M.D.; Manzoni, C.; Rademakers, R.; Graff-Radford, N.R.; Dickson, D.W.; et al.
2015A candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMSRosmarin, D.; Palles, C.; Pagnamenta, A.; Kaur, K.; Pita, G.; Martin, M.; Domingo, E.; Jones, A.; Howarth, K.; Freeman-Mills, L.; Johnstone, E.; Wang, H.; Love, S.; Scudder, C.; Julier, P.; Fernández-Rozadilla, C.; Ruiz-Ponte, C.; Carracedo, A.; Castellvi-Bel, S.; Castells, A.; et al.
2012A case series of five Sri Lankan patients with ovotesticular disorder of sex developmentWettasinghe, K.; Sirisena, N.; Andraweera, P.; Jayasekara, R.; Dissanayake, V.
2012A clinical approach to the investigation of suspected vaccine anaphylaxisGold, M.
1995A clinically mild case of mucopolysaccharidosis type I - Scheie syndrome (case report)Kozlowski, K.; Nicol, R.; Hopwood, J.
2004A combined 13CO2/H2 breath test can be used to assess starch digestion and fermentation in humansSymonds, E.; Kritas, S.; Omari, T.; Butler, R.
2005A common mitchondrial DNA variant is associated with thinness in mothers and their 20-yr-old offspringParker, E.; Phillips, D.; Cockington, R.; Cull, C.; Poulton, J.
2006A comparison of booster immunisation with a combination DTPa-IPV vaccine or DTPa plus IPV in separate injections when co-administered with MMR, at age 4-6 yearsMarshall, H.; Nolan, T.; Roberton, D.; Richmond, P.; Lambert, S.; Jacquet, J.; Schuerman, L.
2010A comparison of oral narratives in children with specific language and non-specific language impairmentPearce, W.; James, D.; McCormack, P.