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Results 1-10 of 15 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2015Growth trajectories in early childhood, their relationship with antenatal and postnatal factors, and development of obesity by age 9 years: results from an Australian birth cohort studyGiles, L.; Whitrow, M.; Davies, M.; Davies, C.; Rumbold, A.; Moore, V.
2015The Importance of Efficacy: Using the Extended Parallel Process Model to Examine Factors Related to Preschool-Age Children Enrolled in Medicaid Receiving Preventive Dental VisitsAskelson, N.M.; Chi, D.L.; Momany, E.T.; Kuthy, R.A.; Carter, K.D.; Field, K.; Damiano, P.C.
2015Exclusive breastfeeding duration during the first 6 months of life is positively associated with length-for-age among infants 6-12 months old, in Mangochi district, MalawiKamudoni, P.; Maleta, K.; Shi, Z.; Holmboe-Ottesen, G.
2015Butanolysis derivatization: improved sensitivity in LC-MS/MS quantitation of heparan sulfate in urine from mucopolysaccharidosis patientsTrim, P.; Hopwood, J.; Snel, M.
2015The prevalence of non-alcoholic fatty liver disease in children and adolescents: a systematic review and meta-analysisAnderson, E.; Howe, L.; Jones, H.; Higgins, J.; Lawlor, D.; Fraser, A.; Wong, V.
2015Accuracy of two motor assessments during the first year of life in preterm infants for predicting motor outcome at preschool ageSpittle, A.J.; Lee, K.J.; Spencer-Smith, M.; Lorefice, L.E.; Anderson, P.J.; Doyle, L.W.; Parikh, N.A.
2015Bone marrow recovery by morphometry during induction chemotherapy for acute lymphoblastic leukemia in childrenNguyen, T.; Melville, A.; Nath, S.; Story, C.; Howell, S.; Sutton, R.; Zannettino, A.; Revesz, T.; Bandapalli, O.
2015Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activityBrookes, E.; Laurent, B.; Õunap, K.; Carroll, R.; Moeschler, J.; Field, M.; Schwartz, C.; Gecz, J.; Shi, Y.
2015Exclusive breastfeeding and risk of dental malocclusionPeres, K.; Cascaes, A.; Peres, M.; Demarco, F.; Santos, I.; Matijasevich, A.; Barros, A.
2015Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorderKumar, R.; Corbett, M.; Smith, N.; Jolly, L.; Tan, C.; Keating, D.; Duffield, M.; Utsumi, T.; Moriya, K.; Smith, K.; Hoischen, A.; Abbott, K.; Harbord, M.; Compton, A.; Woenig, J.; Arts, P.; Kwint, M.; Wieskamp, N.; Gijsen, S.; Veltman, J.; et al.

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