Rezultati - Kranz, Peter G

Cerebral Air Embolism from Angioinvasive Cavitary Aspergillosis od 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 od 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 od 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() od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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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