Case Report: A COVID-19 Patient Presenting with Mild Rhabdomyolysis

Por Borku Uysal, Betul, Ikitimur, Hande, Yavuzer, Serap, Islamoglu, Mehmet Sami, Cengiz, Mahir
Publicado no Am J Trop Med Hyg (2020)

Most notable 100 articles of COVID-19: an Altmetric study based on bibliometric analysis

Por Borku Uysal, Betul, Islamoglu, Mehmet Sami, Koc, Suna, Karadag, Mehmet, Dokur, Mehmet
Publicado no Ir J Med Sci (2021)

Effect of oral l-Glutamine supplementation on Covid-19 treatment

Por Cengiz, Mahir, Borku Uysal, Betul, Ikitimur, Hande, Ozcan, Erkan, Islamoğlu, Mehmet Sami, Aktepe, Emre, Yavuzer, Hakan, Yavuzer, Serap
Publicado no Clin Nutr Exp (2020)

Human Cerebrospinal Fluid Induces Neuronal Excitability Changes in Resected Human Neocortical and Hippocampal Brain Slices

Por Wickham, Jenny, Corna, Andrea, Schwarz, Niklas, Uysal, Betül, Layer, Nikolas, Honegger, Jürgen B., Wuttke, Thomas V., Koch, Henner, Zeck, Günther
Publicado no Front Neurosci (2020)

Impaired Corneal Biomechanical Properties and the Prevalence of Keratoconus in Mitral Valve Prolapse

Por Kalkan Akcay, Emine, Akcay, Murat, Uysal, Betul Seher, Kosekahya, Pinar, Aslan, Abdullah Nabi, Caglayan, Mehtap, Koseoglu, Cemal, Yulek, Fatma, Cagil, Nurullah
Publicado em 2014

Determining host factors contributing to disease severity in a family cluster of 29 hospitalized SARS‐CoV‐2 patients: Could genetic factors be relevant in the clinical course of CO...

Por Ikitimur, Hande, Borku Uysal, Betul, Cengiz, Mahir, Ikitimur, Barış, Uysal, Harun, Ozcan, Erkan, Islamoglu, Mehmet Sami, Seyhan, Serhat, Yavuzer, Hakan, Yavuzer, Serap
Publicado no J Med Virol (2020)

Tocilizumab challenge: A series of cytokine storm therapy experiences in hospitalized COVID‐19 pneumonia patients

Por Borku Uysal, Betul, Ikitimur, Hande, Yavuzer, Serap, Ikitimur, Baris, Uysal, Harun, Islamoglu, Mehmet Sami, Ozcan, Erkan, Aktepe, Emre, Yavuzer, Hakan, Cengiz, Mahir
Publicado no J Med Virol (2020)

Can Positron Emission Tomography and Computed Tomography Be a Substitute for Bone Marrow Biopsy in Detection of Bone Marrow Involvement in Patients with Hodgkin’s or Non-Hodgkin’s...

Por Çetin, Güven, Çıkrıkçıoğlu, M. Ali, Özkan, Tuba, Karatoprak, Cumali, Ar, M. Cem, Eşkazan, Ahmet Emre, Ayer, Mesut, Cerit, Abdullah, Gözübenli, Kübra, Börkü Uysal, Betül, Erdem, Simge, Ergül, Nurhan, Tatar, Gamze, Çermik, T. Fikret
Publicado no Turk J Haematol (2015)

Long-term adult human brain slice cultures as a model system to study human CNS circuitry and disease

Por Schwarz, Niklas, Uysal, Betül, Welzer, Marc, Bahr, Jacqueline C, Layer, Nikolas, Löffler, Heidi, Stanaitis, Kornelijus, PA, Harshad, Weber, Yvonne G, Hedrich, Ulrike BS, Honegger, Jürgen B, Skodras, Angelos, Becker, Albert J, Wuttke, Thomas V, Koch, Henner
Publicado no eLife (2019)

In Vitro Differentiated Human Stem Cell-Derived Neurons Reproduce Synaptic Synchronicity Arising during Neurodevelopment

Por Rosa, Filip, Dhingra, Ashutosh, Uysal, Betül, Mendis, G. Dulini C., Loeffler, Heidi, Elsen, Gina, Mueller, Stephan, Schwarz, Niklas, Castillo-Lizardo, Melissa, Cuddy, Claire, Becker, Felicitas, Heutink, Peter, Reid, Christopher A., Petrou, Steven, Lerche, Holger, Maljevic, Snezana
Publicado no Stem Cell Reports (2020)

De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias

Por Helbig, Katherine L., Lauerer, Robert J., Bahr, Jacqueline C., Souza, Ivana A., Myers, Candace T., Uysal, Betül, Schwarz, Niklas, Gandini, Maria A., Huang, Sun, Keren, Boris, Mignot, Cyril, Afenjar, Alexandra, Billette de Villemeur, Thierry, Héron, Delphine, Nava, Caroline, Valence, Stéphanie, Buratti, Julien, Fagerberg, Christina R., Soerensen, Kristina P., Kibaek, Maria, Kamsteeg, Erik-Jan, Koolen, David A., Gunning, Boudewijn, Schelhaas, H. Jurgen, Kruer, Michael C., Fox, Jordana, Bakhtiari, Somayeh, Jarrar, Randa, Padilla-Lopez, Sergio, Lindstrom, Kristin, Jin, Sheng Chih, Zeng, Xue, Bilguvar, Kaya, Papavasileiou, Antigone, Xin, Qinghe, Zhu, Changlian, Boysen, Katja, Vairo, Filippo, Lanpher, Brendan C., Klee, Eric W., Tillema, Jan-Mendelt, Payne, Eric T., Cousin, Margot A., Kruisselbrink, Teresa M., Wick, Myra J., Baker, Joshua, Haan, Eric, Smith, Nicholas, Corbett, Mark A., MacLennan, Alastair H., Gecz, Jozef, Biskup, Saskia, Goldmann, Eva, Rodan, Lance H., Kichula, Elizabeth, Segal, Eric, Jackson, Kelly E., Asamoah, Alexander, Dimmock, David, McCarrier, Julie, Botto, Lorenzo D., Filloux, Francis, Tvrdik, Tatiana, Cascino, Gregory D., Klingerman, Sherry, Neumann, Catherine, Wang, Raymond, Jacobsen, Jessie C., Nolan, Melinda A., Snell, Russell G., Lehnert, Klaus, Sadleir, Lynette G., Anderlid, Britt-Marie, Kvarnung, Malin, Guerrini, Renzo, Friez, Michael J., Lyons, Michael J., Leonhard, Jennifer, Kringlen, Gabriel, Casas, Kari, El Achkar, Christelle M., Smith, Lacey A., Rotenberg, Alexander, Poduri, Annapurna, Sanchis-Juan, Alba, Carss, Keren J., Rankin, Julia, Zeman, Adam, Raymond, F. Lucy, Blyth, Moira, Kerr, Bronwyn, Ruiz, Karla, Urquhart, Jill, Hughes, Imelda, Banka, Siddharth, Hedrich, Ulrike B.S., Scheffer, Ingrid E., Helbig, Ingo, Zamponi, Gerald W., Lerche, Holger, Mefford, Heather C.
Publicado no Am J Hum Genet (2018)

De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias

Por Helbig, Katherine L., Lauerer, Robert J., Bahr, Jacqueline C., Souza, Ivana A., Myers, Candace T., Uysal, Betül, Schwarz, Niklas, Gandini, Maria A., Huang, Sun, Keren, Boris, Mignot, Cyril, Afenjar, Alexandra, Billette de Villemeur, Thierry, Héron, Delphine, Nava, Caroline, Valence, Stéphanie, Buratti, Julien, Fagerberg, Christina R., Soerensen, Kristina P., Kibaek, Maria, Kamsteeg, Erik-Jan, Koolen, David A., Gunning, Boudewijn, Schelhaas, H. Jurgen, Kruer, Michael C., Fox, Jordana, Bakhtiari, Somayeh, Jarrar, Randa, Padilla-Lopez, Sergio, Lindstrom, Kristin, Jin, Sheng Chih, Zeng, Xue, Bilguvar, Kaya, Papavasileiou, Antigone, Xing, Qinghe, Zhu, Changlian, Boysen, Katja, Vairo, Filippo, Lanpher, Brendan C., Klee, Eric W., Tillema, Jan-Mendelt, Payne, Eric T., Cousin, Margot A., Kruisselbrink, Teresa M., Wick, Myra J., Baker, Joshua, Haan, Eric, Smith, Nicholas, Sadeghpour, Azita, Davis, Erica E., Katsanis, Nicholas, Corbett, Mark A., MacLennan, Alastair H., Gecz, Jozef, Biskup, Saskia, Goldmann, Eva, Rodan, Lance H., Kichula, Elizabeth, Segal, Eric, Jackson, Kelly E., Asamoah, Alexander, Dimmock, David, McCarrier, Julie, Botto, Lorenzo D., Filloux, Francis, Tvrdik, Tatiana, Cascino, Gregory D., Klingerman, Sherry, Neumann, Catherine, Wang, Raymond, Jacobsen, Jessie C., Nolan, Melinda A., Snell, Russell G., Lehnert, Klaus, Sadleir, Lynette G., Anderlid, Britt-Marie, Kvarnung, Malin, Guerrini, Renzo, Friez, Michael J., Lyons, Michael J., Leonhard, Jennifer, Kringlen, Gabriel, Casas, Kari, El Achkar, Christelle M., Smith, Lacey A., Rotenberg, Alexander, Poduri, Annapurna, Sanchis-Juan, Alba, Carss, Keren J., Rankin, Julia, Zeman, Adam, Raymond, F. Lucy, Blyth, Moira, Kerr, Bronwyn, Ruiz, Karla, Urquhart, Jill, Hughes, Imelda, Banka, Siddharth, Hedrich, Ulrike B.S., Scheffer, Ingrid E., Helbig, Ingo, Zamponi, Gerald W., Lerche, Holger, Mefford, Heather C.
Publicado no Am J Hum Genet (2019)