Vivi Sury

A mutation in the saposin A coding region of the prosaposin gene in an infant presenting as Krabbe disease: first report of saposin A deficiency in humans

Ronen Spiegel, Gideon Bach, Vivi Sury et al. · Molecular Genetics and Metabolism · 2004 · 130 citations

Life Sciences, Genetics, Molecular Genetics +3

The clinical spectrum of fetal Niemann–Pick type C

Ronen Spiegel, Annick Raas‐Rothschild, Orit Reish et al. · American Journal of Medical Genetics Part A · 2009 · 96 citations

Medicine, Pediatrics, Maternal-fetal Medicine +6

A novel SCARB2 mutation in progressive myoclonus epilepsy indicated by reduced β-glucocerebrosidase activity

Marsha Zeigler, Vardiella Meiner, J. P. Newman et al. · Journal of the Neurological Sciences · 2014 · 22 citations

Medicine, Genetics, Neurology +15

The identification of lysosomal ganglioside sialidase in human cells

Marcia Zeigler, Vivi Sury, Gideon Bach · European Journal of Biochemistry · 1989 · 19 citations · Full text

Life Sciences, Biochemistry, Cell Biology +6

Genetic screening for Krabbe disease: Learning from the past and looking to the future

Michal Macarov, Joël Zlotogora, Vardiella Meiner et al. · American Journal of Medical Genetics Part A · 2011 · 11 citations

Life Sciences, Genetics, Obstetrics +14