Alexander disease with serial MRS and a new mutation in the glial fibrillary acidic protein geneBASSUK, A. G; JOSHI, A; BURTON, B. K et al.Neurology. 2003, Vol 61, Num 7, pp 1014-1015, issn 0028-3878, 2 p.Article

Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunctionSOWERS, L. P; LOO, L; EL-SHANTI, H et al.Molecular psychiatry. 2013, Vol 18, Num 10, pp 1077-1089, issn 1359-4184, 13 p.Article

A child with spinal cord AVM presenting with raised intracranial pressureBASSUK, A. G; BURROWES, D. M; VELIMIROVIC, B et al.Neurology. 2003, Vol 60, Num 10, pp 1724-1725, issn 0028-3878, 2 p.Article

Contribution of VANGL2 mutations to isolated neural tube defectsKIBAR, Z; SALEM, S; BOSOI, C. M et al.Clinical genetics. 2011, Vol 80, Num 1, pp 76-82, issn 0009-9163, 7 p.Article

Activation of the granulocyte-macrophage colony-stimulating factor promoter in T cells requires cooperative binding of Elf-1 and AP-1 transcription factorsCHUNG-YIH WANG; BASSUK, A. G; BOISE, L. H et al.Molecular and cellular biology (Print). 1994, Vol 14, Num 2, pp 1153-1159, issn 0270-7306Article

SCARB2 Mutations in Progressive Myoclonus Epilepsy (PME) Without Renal FailureDIBBENS, L. M; MICHDUCCI, R; WALLACE, R et al.Annals of neurology. 2009, Vol 66, Num 4, pp 532-536, issn 0364-5134, 5 p.Article

In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndromeBASSUK, A. G; CHEN, Y. Z; BATISH, S. D et al.Neurogenetics (Oxford. Print). 2007, Vol 8, Num 1, pp 45-49, issn 1364-6745, 5 p.Article

Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10RAMPERSAUD, E; BASSUK, A. G; BODURTHA, J et al.Journal of medical genetics. 2005, Vol 42, Num 12, pp 940-946, issn 0022-2593, 7 p.Article