Perfusion MRI: The Five Most Frequently Asked Technical Questions

Por Essig, Marco, Shiroishi, Mark S., Nguyen, Thanh Binh, Saake, Marc, Provenzale, James M., Enterline, David, Anzalone, Nicoletta, Dörfler, Arnd, Rovira, Àlex, Wintermark, Max, Law, Meng
Publicado em 2013

Perfusion MRI: The Five Most Frequently Asked Clinical Questions

Por Essig, Marco, Nguyen, Thanh Binh, Shiroishi, Mark S., Saake, Marc, Provenzale, James M., Enterline, David S., Anzalone, Nicoletta, Dörfler, Arnd, Rovira, Àlex, Wintermark, Max, Law, Meng
Publicado em 2013

Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari Type I Malformation

Por MARKUNAS, CHRISTINA A., ENTERLINE, DAVID S., DUNLAP, KAITLYN, SOLDANO, KAREN, COPE, HEIDI, STAJICH, JEFFREY, GRANT, GERALD, FUCHS, HERBERT, GREGORY, SIMON G., ASHLEY-KOCH, ALLISON E.
Publicado em 2013

Stent-assisted coil emboilization of ruptured intracranial aneurysms: A retrospective multicenter review

Por Golshani, Kiarash, Ferrel, Andrew, Lessne, Mark, Shah, Pratish, Chowdhary, Abhineet, Choulakian, Armen, Alexander, Michael J., Smith, Tony P., Enterline, David S., Zomorodi, Ali R., Britz, Gavin W.
Publicado em 2012

Stratified Whole Genome Linkage Analysis of Chiari Type I Malformation Implicates Known Klippel-Feil Syndrome Genes as Putative Disease Candidates

Por Markunas, Christina A., Soldano, Karen, Dunlap, Kaitlyn, Cope, Heidi, Asiimwe, Edgar, Stajich, Jeffrey, Enterline, David, Grant, Gerald, Fuchs, Herbert, Gregory, Simon G., Ashley-Koch, Allison E.
Publicado em 2013

Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics

Por Markunas, Christina A, Lock, Eric, Soldano, Karen, Cope, Heidi, Ding, Chien-Kuang C, Enterline, David S, Grant, Gerald, Fuchs, Herbert, Ashley-Koch, Allison E, Gregory, Simon G
Publicado em 2014

Neural Tube Defects and Folate Pathway Genes: Family-Based Association Tests of Gene–Gene and Gene–Environment Interactions

Por Boyles, Abee L., Billups, Ashley V., Deak, Kristen L., Siegel, Deborah G., Mehltretter, Lorraine, Slifer, Susan H., Bassuk, Alexander G., Kessler, John A., Reed, Michael C., Nijhout, H. Frederik, George, Timothy M., Enterline, David S., Gilbert, John R., Speer, Marcy C.
Publicado em 2006

SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects

Por Deak, Kristen L., Boyles, Abee L., Etchevers, Heather C., Melvin, Elizabeth C., Siegel, Deborah G., Graham, Felicia L., Slifer, Susan H., Enterline, David S., George, Timothy M., Vekemans, Michel, McClay, David, Bassuk, Alexander G., Kessler, John A., Linney, Elwood, Gilbert, John R., Speer, Marcy C.
Publicado em 2005

LGG-08. A PHASE II PROSPECTIVE STUDY OF SELUMETINIB IN CHILDREN WITH RECURRENT OR REFRACTORY LOW-GRADE GLIOMA (LGG): A PEDIATRIC BRAIN TUMOR CONSORTIUM (PBTC) STUDY

Por Fangusaro, Jason, Onar-Thomas, Arzu, Poussaint, Tina Y, Wu, Shengjie, Ligon, Azra H, Lindeman, Neal, Banerjee, Anu, Packer, Roger J, Kilburn, Lindsay B, Pollack, Ian F, Jakacki, Regina I, Qaddoumi, Ibrahim, Fisher, Paul G, Dhall, Girish, Baxter, Patricia, Kreissman, Susan G, Stewart, Clinton F, Pfister, Stefan M, Jones, David TW, Vezina, Gilbert, Stern, Jessica, Panigrahy, Ashok, Jones, Blaise V, Patay, Zoltan, Tamrazi, Benita, Jones, Jeremy Y, Haque, Sofia S, Enterline, David S, Cha, Soonmee, Doyle, Laurence A, Smith, Malcolm, Boyett, James M, Dunkel, Ira J, Fouladi, Maryam
Publicado no Neuro Oncol (2017)