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Results 61-70 of 483 (Search time: 0.005 seconds).
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PreviewIssue DateTitleAuthor(s)
2000Saposins A,B,C, and D in plasma of patients with lysosomal storage disordersChang, M.; Bindloss, C.; Grabowski, G.; Qi, X.; Winchester, B.; Hopwood, J.; Meikle, P.
2000Epidemic of schizophrenia in children or inappropriate prescribing?Jureidini, J.
2023Heatwaves and wildfires suffocate our healthy start to life: time to assess impact and take action.Bansal, A.; Cherbuin, N.; Davis, D.L.; Peek, M.J.; Wingett, A.; Christensen, B.K.; Carlisle, H.; Broom, M.; Schoenaker, D.A.J.M.; Dahlstrom, J.E.; Phillips, C.B.; Vardoulakis, S.; Nanan, R.; Nolan, C.J.
2023The unfinished agenda of communicable diseases among children and adolescents before the COVID-19 pandemic, 1990–2019: a systematic analysis of the Global Burden of Disease Study 2019Sharew, N.T.
2020Coronavirus disease 2019 in patients with inborn errors of immunity: an international studyMeyts, I.; Bucciol, G.; Quinti, I.; Neven, B.; Fischer, A.; Seoane, E.; Lopez-Granados, E.; Gianelli, C.; Robles-Marhuenda, A.; Jeandel, P.Y.; Paillard, C.; Sankaran, V.G.; Demirdag, Y.Y.; Lougaris, V.; Aiuti, A.; Plebani, A.; Milito, C.; Dalm, V.A.; Guevara-Hoyer, K.; Sánchez-Ramón, S.; et al.
2021Diet quality trajectories and cardiovascular phenotypes/metabolic syndrome risk by 11-12 yearsKerr, J.A.; Liu, R.S.; Gasser, C.E.; Mensah, F.K.; Burgner, D.; Lycett, K.; Gillespie, A.N.; Juonala, M.; Clifford, S.A.; Olds, T.; Saffery, R.; Gold, L.; Liu, M.; Azzopardi, P.; Edwards, B.; Dwyer, T.; Wake, M.
2019GJB2 and GJB6 mutations in hereditary recessive non-syndromic hearing impairment in CameroonTingang Wonkam, E.; Chimusa, E.; Noubiap, J.J.; Adadey, S.M.; F Fokouo, J.V.; Wonkam, A.
2019Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2Corbett, M.A.; Kroes, T.; Veneziano, L.; Bennett, M.F.; Florian, R.; Schneider, A.L.; Coppola, A.; Licchetta, L.; Franceschetti, S.; Suppa, A.; Wenger, A.; Mei, D.; Pendziwiat, M.; Kaya, S.; Delledonne, M.; Straussberg, R.; Xumerle, L.; Regan, B.; Crompton, D.; van Rootselaar, A.-F.; et al.
2019Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmissionGuo, H.; Li, Y.; Shen, L.; Wang, T.; Jia, X.; Liu, L.; Xu, T.; Ou, M.; Hoekzema, K.; Wu, H.; Gillentine, M.A.; Liu, C.; Ni, H.; Peng, P.; Zhao, R.; Zhang, Y.; Phornphutkul, C.; Stegmann, A.P.A.; Prada, C.E.; Hopkin, R.J.; et al.
2007Stressed mucosaDavidson, G.; Kritas, S.; Butler, R.; Cooke, R.J.; Vandenplas, Y.; Wahn, U.

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