The association between mutations in the lysosomal protein glucocerebrosidase and parkinsonism

Por DePaolo, J., Goker-Alpan, O., Samaddar, T., Lopez, G., Sidransky, E.
Publicado em 2009

Divergent phenotypes in Gaucher disease implicate the role of modifiers

Por Goker-Alpan, O, Hruska, K, Orvisky, E, Kishnani, P, Stubblefield, B, Schiffmann, R, Sidransky, E
Publicado em 2005

UNIPARENTAL DISOMY OF CHROMOSOME 1 CAUSING CONCURRENT CHARCOT-MARIE-TOOTH AND GAUCHER DISEASE TYPE 3

Por Benko, W.S., Hruska, K.S., Nagan, N., Goker-Alpan, O., Hart, P.S., Schiffmann, R., Sidransky, E.
Publicado no Neurology (2008)

Parkinsonism among Gaucher disease carriers

Por Goker-Alpan, O, Schiffmann, R, LaMarca, M, Nussbaum, R, McInerney-Leo, A, Sidransky, E
Publicado em 2004

Bilateral Symmetrical Cortical Osteolytic Lesions in Two Patients with Gaucher Disease

Por Oppenheim, IM, Medina Canon, A, Barcenas, W, Groden, C, Goker-Alpan, O, Resnik, C, Sidransky, E
Publicado em 2011