Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centres

di Vellodi, A, Young, E, Cooper, A, Wraith, J, Winchester, B, Meaney, C, Ramaswami, U, Will, A
Pubblicazione 1997

Screening for medium chain acyl-CoA dehydrogenase deficiency using electrospray ionisation tandem mass spectrometry

di Clayton, P., Doig, M., Ghafari, S., Meaney, C., Taylor, C., Leonard, J., Morris, M., Johnson, A.
Pubblicazione 1998

Characteristics and outcomes of women initiating ART during pregnancy versus breastfeeding in Option B+ in Malawi

di Landes, M., Sodhi, S., Matengeni, A., Meaney, C., van Lettow, M., Chan, A. K., van Oosterhout, J. J.
Pubblicato in BMC Public Health (2016)

Prevalence of SAP gene defects in male patients diagnosed with common variable immunodeficiency

di EASTWOOD, D, GILMOUR, K C, NISTALA, K, MEANEY, C, CHAPEL, H, SHERRELL, Z, WEBSTER, A D, DAVIES, E G, Jones, A, GASPAR, H B
Pubblicazione 2004

Roles of Education and IQ in Cognitive Reserve in Parkinson's Disease-Mild Cognitive Impairment

di Armstrong, M.J., Naglie, G., Duff-Canning, S., Meaney, C., Gill, D., Eslinger, P.J., Zadikoff, C., Mapstone, M., Chou, K.L., Persad, C., Litvan, I., Mast, B.T., Fox, S., Tang-Wai, D.F., Marras, C.
Pubblicazione 2012

Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers

di Marras, C., Schuele, B., Munhoz, R.P., Rogaeva, E., Langston, J.W., Kasten, M., Meaney, C., Klein, C., Wadia, P.M., Lim, S.-Y., Chuang, R.S.-I., Zadikof, C., Steeves, T., Prakash, K.M., de Bie, R.M.A., Adeli, G., Thomsen, T., Johansen, K.K., Teive, H.A., Asante, A., Reginold, W., Lang, A.E.
Pubblicazione 2011