Becoming a Physician Scientist: A View Looking up from Base Camp

Por Ganetzky, Rebecca D.
Publicado no Acad Med (2017)

8-year retrospective analysis of intravenous arginine therapy for acute metabolic strokes in pediatric mitochondrial disease

Por Ganetzky, Rebecca D., Falk, Marni J.
Publicado no Mol Genet Metab (2018)

Microvascular endothelial dysfunction in mitochondrial stroke-like episodes supports use of intravenous l-arginine

Por Ganetzky, Rebecca D., Falk, Marni J.
Publicado no Mol Genet Metab Rep (2018)

Argininosuccinic Acid Lyase Deficiency Missed by Newborn Screen

Por Ganetzky, Rebecca D., Bedoukian, Emma, Deardorff, Matthew A., Ficicioglu, Can
Publicado no JIMD Rep (2016)

ECHS1 Deficiency as a Cause of Severe Neonatal Lactic Acidosis

Por Ganetzky, Rebecca D., Bloom, Kaitlyn, Ahrens-Nicklas, Rebecca, Edmondson, Andrew, Deardorff, Matthew A., Bennett, Michael J., Ficicioglu, Can
Publicado no JIMD Rep (2016)

Cytokine signature profiles in acquired aplastic anemia and myelodysplastic syndromes

Por Feng, Xingmin, Scheinberg, Phillip, Wu, Colin O., Samsel, Leigh, Nunez, Olga, Prince, Courtney, Ganetzky, Rebecca D., McCoy, J. Philip, Maciejewski, Jaroslaw P., Young, Neal S.
Publicado em 2011

Hospitalizations for mitochondrial disease across the lifespan in the U.S

Por McCormack, Shana E., Xiao, Rui, Kilbaugh, Todd J., Karlsson, Michael, Ganetzky, Rebecca D., Cunningham, Zarazuela Zolkipli, Goldstein, Amy, Falk, Marni J., Damrauer, Scott M.
Publicado no Mol Genet Metab (2017)

USMG5 Ashkenazi Jewish founder mutation impairs mitochondrial complex V dimerization and ATP synthesis

Por Barca, Emanuele, Ganetzky, Rebecca D, Potluri, Prasanth, Juanola-Falgarona, Marti, Gai, Xiaowu, Li, Dong, Jalas, Chaim, Hirsch, Yoel, Emmanuele, Valentina, Tadesse, Saba, Ziosi, Marcello, Akman, Hasan O, Chung, Wendy K, Tanji, Kurenai, McCormick, Elizabeth M, Place, Emily, Consugar, Mark, Pierce, Eric A, Hakonarson, Hakon, Wallace, Douglas C, Hirano, Michio, Falk, Marni J
Publicado no Hum Mol Genet (2018)