Cerebral Air Embolism from Angioinvasive Cavitary Aspergillosis

gan Lin, Chen, Barrio, George A., Hurwitz, Lynne M., Kranz, Peter G.
Cyhoeddwyd 2014

Use of Apparent Diffusion Coefficient Values for Diagnosis of Pediatric Posterior Fossa Tumors

gan Pierce, Theodore, Kranz, Peter G, Roth, Christopher, Leong, Dalun, Wei, Peter, Provenzale, James M
Cyhoeddwyd 2014

Effect of Body Habitus on Radiation Dose During CT Fluoroscopy-Guided Spine Injections

gan Viola, Ronald J., Nguyen, Giao B., Yoshizumi, Terry T., Stinnett, Sandra S., Hoang, Jenny K., Kranz, Peter G.
Cyhoeddwyd yn Interv Neuroradiol (2014)

Cross-sectional CT Assessment of the Extent of Injectate Spread at CT Fluoroscopy–guided Cervical Epidural Interlaminar Steroid Injections

gan Amrhein, Timothy J., Bozdogan, Erol, Vekaria, Sunit, Patel, Prasad, Lerebours, Reginald, Luo, Sheng, Kranz, Peter G.
Cyhoeddwyd yn Radiology (2019)

Predictors of Late Neurological Deterioration After Spontaneous Intracerebral Hemorrhage

gan Sun, Weiping, Pan, Wenqin, Kranz, Peter G., Hailey, Claire E., Williamson, Rachel A., Sun, Wei, Laskowitz, Daniel T., James, Michael L.
Cyhoeddwyd 2013

Reorganization and Stability for Motor and Language Areas Using Cortical Stimulation: Case Example and Review of the Literature

gan Serafini, Sandra, Komisarow, Jordan M., Gallentine, William, Mikati, Mohamad A., Bonner, Melanie J., Kranz, Peter G., Haglund, Michael M., Grant, Gerald
Cyhoeddwyd 2013

Malignant brainstem gliomas in adults: clinicopathological characteristics and prognostic factors

gan Babu, Ranjith, Kranz, Peter G., Agarwal, Vijay, McLendon, Roger E., Thomas, Steven, Friedman, Allan H., Bigner, Darell D., Adamson, Cory
Cyhoeddwyd yn J Neurooncol (2014)

Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms

gan Shashi, Vandana, Francis, Alan, Hooper, Stephen R, Kranz, Peter G, Zapadka, Michael, Schoch, Kelly, Ip, Edward, Tandon, Neeraj, Howard, Timothy D, Keshavan, Matcheri S
Cyhoeddwyd 2012

Comparison of Acoustic Radiation Force Impulse Imaging Derived Carotid Plaque Stiffness with Spatially Registered MRI Determined Composition

gan Doherty, Joshua R., Dahl, Jeremy J., Kranz, Peter G., El Husseini, Nada, Chang, Hing-Chiu, Chen, Nan-kuei, Allen, Jason D., Ham, Katherine L., Trahey, Gregg E.
Cyhoeddwyd yn IEEE Trans Med Imaging (2015)

Gender and Age Interact to Affect Early Outcome after Intracerebral Hemorrhage

gan Umeano, Odera, Phillips-Bute, Barbara, Hailey, Claire E., Sun, Wei, Gray, Marisa C., Roulhac-Wilson, Briana, McDonagh, David L., Kranz, Peter G., Laskowitz, Daniel T., James, Michael L.
Cyhoeddwyd 2013

A Novel, Reproducible, and Objective Method for Volumetric Magnetic Resonance Imaging Assessment of Enhancing Glioblastoma

gan Kanaly, Charles W., Mehta, Ankit I., Ding, Dale, Hoang, Jenny, Kranz, Peter G., Herndon, James E., Coan, April, Crocker, Ian, Waller, Anthony F., Friedman, Allan H., Reardon, David A., Sampson, John H.
Cyhoeddwyd yn J Neurosurg (2014)

Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder

gan Liu, Ning, Schoch, Kelly, Luo, Xi, Pena, Loren D M, Bhavana, Venkata Hemanjani, Kukolich, Mary K, Stringer, Sarah, Powis, Zöe, Radtke, Kelly, Mroske, Cameron, Deak, Kristen L, McDonald, Marie T, McConkie-Rosell, Allyn, Markert, M Louise, Kranz, Peter G, Stong, Nicholas, Need, Anna C, Bick, David, Amaral, Michelle D, Worthey, Elizabeth A, Levy, Shawn, Wangler, Michael F, Bellen, Hugo J, Shashi, Vandana, Yamamoto, Shinya
Cyhoeddwyd yn Hum Mol Genet (2018)

Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases

gan Pena, Loren DM, Jiang, Yong-Hui, Schoch, Kelly, Spillmann, Rebecca C., Walley, Nicole, Stong, Nicholas, Horn, Sarah Rapisardo, Sullivan, Jennifer A., McConkie-Rosell, Allyn, Kansagra, Sujay, Smith, Edward C., El-Dairi, Mays, Bellet, Jane, Ann Keels, Martha, Jasien, Joan, Kranz, Peter G., Noel, Richard, Nagaraj, Shashi K., Lark, Robert K., Wechsler, Daniel SG, del Gaudio, Daniela, Leung, Marco L., Hendon, Laura G., Parker, Collette C., Jones, Kelly L., Goldstein, David B., Shashi, Vandana
Cyhoeddwyd yn Genet Med (2017)

De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype

gan Shashi, Vandana, Pena, Loren D.M., Kim, Katherine, Burton, Barbara, Hempel, Maja, Schoch, Kelly, Walkiewicz, Magdalena, McLaughlin, Heather M., Cho, Megan, Stong, Nicholas, Hickey, Scott E., Shuss, Christine M., Freemark, Michael S., Bellet, Jane S., Keels, Martha Ann, Bonner, Melanie J., El-Dairi, Maysantoine, Butler, Megan, Kranz, Peter G., Stumpel, Constance T.R.M., Klinkenberg, Sylvia, Oberndorff, Karin, Alawi, Malik, Santer, Rene, Petrovski, Slavé, Kuismin, Outi, Korpi-Heikkilä, Satu, Pietilainen, Olli, Aarno, Palotie, Kurki, Mitja I., Hoischen, Alexander, Need, Anna C., Goldstein, David B., Kortüm, Fanny
Cyhoeddwyd yn Am J Hum Genet (2016)

De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype

gan Shashi, Vandana, Pena, Loren D.M., Kim, Katherine, Burton, Barbara, Hempel, Maja, Schoch, Kelly, Walkiewicz, Magdalena, McLaughlin, Heather M., Cho, Megan, Stong, Nicholas, Hickey, Scott E., Shuss, Christine M., Freemark, Michael S., Bellet, Jane S., Keels, Martha Ann, Bonner, Melanie J., El-Dairi, Maysantoine, Butler, Megan, Kranz, Peter G., Stumpel, Constance T.R.M., Klinkenberg, Sylvia, Oberndorff, Karin, Alawi, Malik, Santer, Rene, Petrovski, Slavé, Kuismin, Outi, Korpi-Heikkilä, Satu, Pietilainen, Olli, Aarno, Palotie, Kurki, Mitja I., Hoischen, Alexander, Need, Anna C., Goldstein, David B., Kortüm, Fanny
Cyhoeddwyd yn Am J Hum Genet (2017)

A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay

gan Schoch, Kelly, Meng, Linyan, Szelinger, Szabolcs, Bearden, David R., Stray-Pedersen, Asbjorg, Busk, Oyvind L., Stong, Nicholas, Liston, Eriskay, Cohn, Ronald D., Scaglia, Fernando, Rosenfeld, Jill A., Tarpinian, Jennifer, Skraban, Cara M., Deardorff, Matthew A., Friedman, Jeremy N., Akdemir, Zeynep Coban, Walley, Nicole, Mikati, Mohamad A., Kranz, Peter G., Jasien, Joan, McConkie-Rosell, Allyn, McDonald, Marie, Wechsler, Stephanie Burns, Freemark, Michael, Kansagra, Sujay, Freedman, Sharon, Bali, Deeksha, Millan, Francisca, Bale, Sherri, Nelson, Stanley F., Lee, Hane, Dorrani, Naghmeh, Goldstein, David B., Xiao, Rui, Yang, Yaping, Posey, Jennifer E., Martinez-Agosto, Julian A., Lupski, James R., Wangler, Michael F., Shashi, Vandana
Cyhoeddwyd yn Am J Hum Genet (2017)

Loss of tubulin deglutamylase CCP1 causes infantile‐onset neurodegeneration

gan Shashi, Vandana, Magiera, Maria M, Klein, Dennis, Zaki, Maha, Schoch, Kelly, Rudnik‐Schöneborn, Sabine, Norman, Andrew, Lopes Abath Neto, Osorio, Dusl, Marina, Yuan, Xidi, Bartesaghi, Luca, De Marco, Patrizia, Alfares, Ahmed A, Marom, Ronit, Arold, Stefan T, Guzmán‐Vega, Francisco J, Pena, Loren DM, Smith, Edward C, Steinlin, Maja, Babiker, Mohamed OE, Mohassel, Payam, Foley, A Reghan, Donkervoort, Sandra, Kaur, Rupleen, Ghosh, Partha S, Stanley, Valentina, Musaev, Damir, Nava, Caroline, Mignot, Cyril, Keren, Boris, Scala, Marcello, Tassano, Elisa, Picco, Paolo, Doneda, Paola, Fiorillo, Chiara, Issa, Mahmoud Y, Alassiri, Ali, Alahmad, Ahmed, Gerard, Amanda, Liu, Pengfei, Yang, Yaping, Ertl‐Wagner, Birgit, Kranz, Peter G, Wentzensen, Ingrid M, Stucka, Rolf, Stong, Nicholas, Allen, Andrew S, Goldstein, David B, Schoser, Benedikt, Rösler, Kai M, Alfadhel, Majid, Capra, Valeria, Chrast, Roman, Strom, Tim M, Kamsteeg, Erik‐Jan, Bönnemann, Carsten G, Gleeson, Joseph G, Martini, Rudolf, Janke, Carsten, Senderek, Jan
Cyhoeddwyd yn EMBO J (2018)