Хайлтын үр дүнгүүд - Kranz, Peter G

Cerebral Air Embolism from Angioinvasive Cavitary Aspergillosis -н 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 -н 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 -н 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() -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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 -н 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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