Anemia risk factors among people living with HIV across the United States in the current treatment era: a clinical cohort study von Harding, B N, Whitney, B M, Nance, R M, Ruderman, S A, Crane, H M, Burkholder, G, Moore, R D, Mathews, W C, Eron, J J, Hunt, P W, Volberding, P, Rodriguez, B, Mayer, K H, Saag, M S, Kitahata, M M, Heckbert, S R, Delaney, J A C

Volltext

Drug resistance in epilepsy: expression of drug resistance proteins in common causes of refractory epilepsy von SISODIYA, S. M, LIN, W.-R, HARDING, B. N, SQUIER, M. V, THOM, M

Volltext

Correlates of psychological intimate partner violence with HIV care outcomes on patients in HIV care von Fredericksen, R J, Nance, R M, Whitney, B M, Harding, B N, Fitzsimmons, E, Del Rio, C, Eron, J, Feaster, D J, Kalokhe, A S, Mathews, W C, Mayer, K H, Metsch, L R, Mugavero, M J, Potter, J, O'Cleirigh, C, Napravnik, S, Rodriguez, B, Ruderman, S, Jac, Delaney, Crane, H M

Volltext

Vascular colocalization of P-glycoprotein, multidrug-resistance associated protein 1, breast cancer resistance protein and major vault protein in human epileptogenic pathologies von Sisodiya, S. M., Martinian, L., Scheffer, G. L., Van Der Valk, P., Scheper, R. J., Harding, B. N., Thom, M.

Volltext

Cajal-Retzius cells, inhibitory interneuronal populations and neuropeptide Y expression in focal cortical dysplasia and microdysgenesis von THOM, M, HARDING, B. N, LIN, W.-R, MARTINIAN, L, CROSS, H, SISODIYA, S. M

Volltext

Deficiency of respiratory chain complex I is a common cause of leigh disease von Morris, A. A. M., Leonard, J. V., Brown, G. K., Bidouki, S. K., Bindoff, L. A., Turnbull, D. M., Woodward, C. E., Harding, A. E., Lake, B. D., Harding, B. N., Farrell, M. A., Bell, J. E., Mirakhur, M.

Volltext

Mcm2 labelling of balloon cells in focal cortical dysplasia von Thom, M., Martinian, L., Sisodiya, S. M., Cross, J. H., Williams, G., Stoeber, K., Harkness, W., Harding, B. N.

Volltext

Persistent reelin-expressing Cajal–Retzius cells in polymicrogyria von Eriksson, S. H., Thom, M., Heffernan, J., Lin, W. R., Harding, B. N., Squier, M. V., Sisodiya, S. M.

Volltext

Dysembryoplastic neuroepithelial tumour Features in 16 patients von Raymond, A. A., Halpin, S. F. S., Alsanjari, N., Cook, M. J., Kitchen, N. D., Fish, D. R., Stevens, J. M., Harding, B. N., Scaravilli, F., Kendall, B., Shorvon, S. D., Neville, B. G. R.

Volltext

Pathogenic factors underlying the lesions in Leigh's disease. Tissue responses to cellular energy deprivation and their clinico-pathological consequences von Cavanagh, J B, Harding, B N

Volltext

Management of Choroid Plexus Tumours in Children: 20 Years Experience at a Single Neurosurgical Centre von McEvoy, Andrew W., Harding, Brian N., Phipps, Kim P., Ellison, David W., Elsmore, Andrew J., Thompson, Dominic, Harkness, William, Hayward, Richard D.

Volltext

Progressive neuronal degeneration of childhood with liver disease (Alpers' disease) presenting in young adults von Harding, B N, Alsanjari, N, Smith, S J, Wiles, C M, Thrush, D, Miller, D H, Scaravilli, F, Harding, A E

Volltext

Central neurocytoma of the cervical spinal cord von STAPLETON, SIMON R, DAVID, KAROLY M, HARKNESS, WILLIAM F J, HARDING, BRIAN N

Volltext

Linkage and Physical Mapping of X-Linked Lissencephaly/SBH (XLIS): A Gene Causing Neuronal Migration Defects in Human Brain von Ross, M. Elizabeth, Allen, Kristina M., Srivastava, Anand K., Featherstone, Terry, Gleeson, Joseph G., Hirsch, Betsy, Harding, Brian N., Andermann, Eva, Abdullah, Rabi, Berg, Michael, Czapansky-Bielman, Desireé, Flanders, Dean J., Guerrini, Renzo, Motté, Jacques, Mira, A. Puche, Scheffer, Ingrid, Berkovic, Samuel, Scaravilli, F., King, Richard A., Ledbetter, David H., Schlessinger, David, Dobyns, William B., Walsh, Christopher A.

Volltext

Cortical neuronal densities and lamination in focal cortical dysplasia von Thom, M, Martinian, L, Sen, A, Cross, J H, Harding, B N, Sisodiya, S M

Volltext

Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndrome von Horslen, S P, Clayton, P T, Harding, B N, Hall, N A, Keir, G, Winchester, B

Volltext

Familial olivopontocerebellar atrophy with neonatal onset: a recessively inherited syndrome with systemic and biochemical abnormalities von Harding, B N, Dunger, D B, Grant, D B, Erdohazi, M

Volltext

Cortical neuronal densities and lamination in focal cortical dysplasia von Thom, M., Martinian, L., Sen, A., Cross, J. H., Harding, B. N., Sisodiya, S. M.

Volltext

Intractable seizures from infancy can be associated with dentato-olivary dysplasia von Harding, B.N., Boyd, S.G.

Volltext

Dentato-olivary dysplasia in sibs: an autosomal recessive disorder? von Martland, T, Harding, B N, Morton, R E, Young, I

Volltext