Common Causes of Uncommon SeizuresEL-BITAR, Mohamad K; BOUSTANY, Rose-Mary N.Pediatric neurology. 2009, Vol 41, Num 2, pp 83-87, issn 0887-8994, 5 p.Article

CLN3p Impacts Galactosylceramide Transport, Raft Morphology, and Lipid ContentRUSYN, Elena; MOUSALLEM, Talal; PERSAUD-SAWIN, Dixie-Ann et al.Pediatric research. 2008, Vol 63, Num 6, pp 625-631, issn 0031-3998, 7 p.Article

Motifs within the CLN3 protein: modulation of cell growth rates and apoptosisPERSAUD-SAWIN, Dixie-Ann N. W; VANDONGEN, Antonius; BOUSTANY, Rose-Mary N et al.Human molecular genetics (Print). 2002, Vol 11, Num 18, pp 2129-2142, issn 0964-6906Article

A 23-year-old man with seizures and visual deficitBOUSTANY, Rose-Mary; BRITTON, Jeffrey W; PARISI, Joseph E et al.Neurology. 2008, Vol 70, Num 1, pp 73-78, issn 0028-3878, 6 p.Article

Neuronal ceroid lipofuscinosis : A common pathway?PERSAUD-SAWIN, Dixie-Ann; MOUSALLEM, Talal; WANG, Christine et al.Pediatric research. 2007, Vol 61, Num 2, pp 146-152, issn 0031-3998, 7 p.Article

A galactosylceramide binding domain is involved in trafficking of CLN3 from Golgi to rafts via recycling endosomesPERSAUD-SAWIN, Dixie-Ann; MCNAMARA, James O; RYLOVA, Svetlana et al.Pediatric research. 2004, Vol 56, Num 3, pp 449-463, issn 0031-3998, 15 p.Article

Impaired cell adhesion and apoptosis in a novel CLN9 Batten disease variantSCHULZ, Angela; DHAR, Sumeer; RYLOVA, Svetlana et al.Annals of neurology. 2004, Vol 56, Num 3, pp 342-350, issn 0364-5134, 9 p.Article

Clinicopathological and molecular characterization of neuronal ceroid lipofuscinosis in the Portuguese populationTEIXEIRA, Carla; GUIMARAES, Antonio; BESSA, Carlos et al.Journal of neurology. 2003, Vol 250, Num 6, pp 661-667, issn 0340-5354, 7 p.Article

The CLN3 gene is a novel molecular target for cancer drug discoveryRYLOVA, Svetlana N; AMALFITANO, Andrea; PERSAUD-SAWIN, Dixie-Ann et al.Cancer research (Baltimore). 2002, Vol 62, Num 3, pp 801-808, issn 0008-5472Article

Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegiaSVENSON, Ingrid K; ASHLEY-KOCH, Allison E; PERICAK-VANCE, Margaret A et al.American journal of human genetics. 2001, Vol 68, Num 5, pp 1077-1085, issn 0002-9297Article

Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegiaASHLEY-KOCH, Allison; BONNER, Erin R; MARCHUK, Douglas A et al.Neurogenetics (Oxford. Print). 2001, Vol 3, Num 2, pp 91-97, issn 1364-6745Article

Mutations in a novel CLN6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinosis in man and mouseHANLIN GAO; BOUSTANY, Rose-Mary N; BRONSON, Roderick T et al.American journal of human genetics. 2002, Vol 70, Num 2, pp 324-335, issn 0002-9297Article