Kết quả tìm kiếm - Kranz, Peter G

Cerebral Air Embolism from Angioinvasive Cavitary Aspergillosis Bằng Lin, Chen, Barrio, George A., Hurwitz, Lynne M., Kranz, Peter G.

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Postsurgical Recurrence of CSF-Venous Fistulas in Spontaneous Intracranial Hypotension Bằng Malinzak, Michael D., Kranz, Peter G., Gray, Linda, Amrhein, Timothy J.

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Use of Apparent Diffusion Coefficient Values for Diagnosis of Pediatric Posterior Fossa Tumors Bằng Pierce, Theodore, Kranz, Peter G, Roth, Christopher, Leong, Dalun, Wei, Peter, Provenzale, James M

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Dual energy CT for the identification of CSF-Venous Fistulas and CSF leaks in spontaneous intracranial hypotension: Report of four cases() Bằng Houk, Jessica L, Marin, Daniele M, Malinzak, Michael D, Kranz, Peter G, Amrhein, Timothy J

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Effect of Body Habitus on Radiation Dose During CT Fluoroscopy-Guided Spine Injections Bằng Viola, Ronald J., Nguyen, Giao B., Yoshizumi, Terry T., Stinnett, Sandra S., Hoang, Jenny K., Kranz, Peter G.

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Cross-sectional CT Assessment of the Extent of Injectate Spread at CT Fluoroscopy–guided Cervical Epidural Interlaminar Steroid Injections Bằng Amrhein, Timothy J., Bozdogan, Erol, Vekaria, Sunit, Patel, Prasad, Lerebours, Reginald, Luo, Sheng, Kranz, Peter G.

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Predictors of Late Neurological Deterioration After Spontaneous Intracerebral Hemorrhage Bằng Sun, Weiping, Pan, Wenqin, Kranz, Peter G., Hailey, Claire E., Williamson, Rachel A., Sun, Wei, Laskowitz, Daniel T., James, Michael L.

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Reorganization and Stability for Motor and Language Areas Using Cortical Stimulation: Case Example and Review of the Literature Bằng Serafini, Sandra, Komisarow, Jordan M., Gallentine, William, Mikati, Mohamad A., Bonner, Melanie J., Kranz, Peter G., Haglund, Michael M., Grant, Gerald

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Malignant brainstem gliomas in adults: clinicopathological characteristics and prognostic factors Bằng Babu, Ranjith, Kranz, Peter G., Agarwal, Vijay, McLendon, Roger E., Thomas, Steven, Friedman, Allan H., Bigner, Darell D., Adamson, Cory

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Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms Bằng Shashi, Vandana, Francis, Alan, Hooper, Stephen R, Kranz, Peter G, Zapadka, Michael, Schoch, Kelly, Ip, Edward, Tandon, Neeraj, Howard, Timothy D, Keshavan, Matcheri S

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Efficacy of epidural blood patching or surgery in spontaneous intracranial hypotension: an evidence map protocol Bằng Amrhein, Timothy J., Kranz, Peter G., Cantrell, Sarah, Deline, Constance R., Carr, Carrie M., Kim, Dong Kun, Goldstein, Karen M., Williams, John W.

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Gender and Age Interact to Affect Early Outcome after Intracerebral Hemorrhage Bằng 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.

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

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

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

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

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

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

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Loss of tubulin deglutamylase CCP1 causes infantile‐onset neurodegeneration Bằng 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

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