Items where Author is "Fachim, H.A."

LOUREIRO, C.M., CORSI-ZUELLI, F., FACHIM, H.A., SHUHAMA, R., MENEZES, P.R., DALTON, C.F., LOUZADA-JUNIOR, P., BELANGERO, S.I.N., COELI-LACCHINI, F.B., REYNOLDS, G.P., LACCHINI, R. and DEL-BEN, C.M. (2023). Effect of D2R, NMDAR and CB1R genetic variants associated with cannabis use and childhood trauma in first-episode psychosis in a Brazilian population [abstract only]. European Psychiatry, 66 (S1), S255-S255.

FACHIM, H.A., CORSI-ZUELLI, F., LOUREIRO, C.M., IAMJAN, S.A., SHUHAMA, R., JOCA, S., MENEZES, P.R., HEALD, A., LOUZADA-JUNIOR, P., DALTON, Caroline, DEL-BEN, C.M. and REYNOLDS, G.P. (2020). Early-life stress effects on BDNF DNA methylation in first-episode psychosis and in rats reared in isolation. Progress in Neuro-Psychopharmacology and Biological Psychiatry, p. 110188.

FACHIM, H.A., LOUREIRO, C.M., SIDDALS, K., DALTON, Caroline, REYNOLDS, G.P., GIBSON, J.M., CHEN, Z.B. and HEALD, A.H. (2020). Circulating microRNA changes in patients with impaired glucose regulation. Adipocyte, 9 (1), 443-453.

FACHIM, H.A., SIDDALS, K., MALIPATIL, N., DONN, R.P., MORENO, G.Y.C., DALTON, Caroline, ADAM, S., SORAN, H., GIBSON, J.M. and HEALD, A.H. (2020). Lifestyle intervention in individuals with impaired glucose regulation affects Caveolin-1 expression and DNA methylation. Adipocyte, 9 (1), 96-107.

LOUREIRO, Camila, FACHIM, H.A., CORSI-ZUELLI, F., MENEZES, P.R., DALTON, Caroline, DEL-BEN, C.M., LOUZADA-JUNIOR, P. and REYNOLDS, Gavin (2019). P.071 Associations between genetic variants of NMDA receptor genes and first episode psychosis in a Brazilian sample. European Neuropsychopharmacology, 29 (6), S68.

FACHIM, H.A., SIDDALS, K., MALIPATIL, N., DONN, R., DALTON, Caroline, GIBSON, M. and HEALD, A (2019). Weight loss in people with impaired glucose regulation affects caveolin-1 (CAV1) expression and DNA methylation in a tissue-specific way. Diabetologia, 62, S138-S138.

WEI, X., ZHANG, S., YANG, W., LUO, Z., SUN, P., DALTON, Caroline, FACHIM, H.A. and REYNOLDS, G.P. (2019). Neuromyelitis optica spectrum disorder in three generations of a Chinese family. Multiple Sclerosis and Related Disorders, 32, 94-96.