Neurologic complications of immune checkpoint inhibitors von Fellner, Avi, Makranz, Chen, Lotem, Michal, Bokstein, Felix, Taliansky, Alisa, Rosenberg, Shai, Blumenthal, Deborah T., Mandel, Jacob, Fichman, Suzana, Kogan, Elena, Steiner, Israel, Siegal, Tali, Lossos, Alexander, Yust-Katz, Shlomit

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A case report of unilateral cervical lymphadenopathy and multiple cranial neuropathies following mRNA-COVID-19 vaccination von Shalabi, Fatma, Lossos, Alexander, Karussis, Dimitrios

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European Association of Neuro-Oncology (EANO) guidelines for treatment of primary central nervous system lymphoma (PCNSL) von Hoang-Xuan, Khê, Deckert, Martina, Ferreri, Andrés J M, Furtner, Julia, Gallego Perez-Larraya, Jaime, Henriksson, Roger, Hottinger, Andreas F, Kasenda, Benjamin, Lefranc, Florence, Lossos, Alexander, McBain, Catherine, Preusser, Matthias, Roth, Patrick, Rudà, Roberta, Schlegel, Uwe, Soffietti, Riccardo, Soussain, Carole, Taphoorn, Martin J B, Touitou, Valérie, Weller, Michael, Bromberg, Jacoline E C

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Amylopectinosis of the fatal epilepsy Lafora disease resists autophagic glycogen catabolism von Wu, Jun, Kakhlon, Or, Weil, Miguel, Lossos, Alexander, Minassian, Berge A

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Short report: Plasma based biomarkers detect radiation induced brain injury in cancer patients treated for brain metastasis: A pilot study von Makranz, Chen, Lubotzky, Asael, Zemmour, Hai, Shemer, Ruth, Glaser, Benjamin, Cohen, Jonathan, Maoz, Myriam, Sapir, Eli, Wygoda, Marc, Peretz, Tamar, Weizman, Noam, Feldman, Jon, Abrams, Ross A, Lossos, Alexander, Dor, Yuval, Zick, Aviad

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MYORG Mutations: a Major Cause of Recessive Primary Familial Brain Calcification von Bauer, Max, Rahat, Dolev, Zisman, Elad, Tabach, Yuval, Lossos, Alexander, Meiner, Vardiella, Arkadir, David

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Germline-driven replication repair-deficient high-grade gliomas exhibit unique hypomethylation patterns von Dodgshun, Andrew J., Fukuoka, Kohei, Edwards, Melissa, Bianchi, Vanessa J., Das, Anirban, Sexton-Oates, Alexandra, Larouche, Valérie, Vanan, Magimairajan I., Lindhorst, Scott, Yalon, Michal, Mason, Gary, Crooks, Bruce, Constantini, Shlomi, Massimino, Maura, Chiaravalli, Stefano, Ramdas, Jagadeesh, Mason, Warren, Ashraf, Shamvil, Farah, Roula, Van Damme, An, Opocher, Enrico, Hamid, Syed Ahmer, Ziegler, David S., Samuel, David, Cole, Kristina A., Tomboc, Patrick, Stearns, Duncan, Thomas, Gregory A., Lossos, Alexander, Sullivan, Michael, Hansford, Jordan R., Mackay, Alan, Jones, Chris, Jones, David T. W., Ramaswamy, Vijay, Hawkins, Cynthia, Bouffet, Eric, Tabori, Uri

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Alleviation of a polyglucosan storage disorder by enhancement of autophagic glycogen catabolism von Kakhlon, Or, Vaknin, Hilla, Mishra, Kumudesh, D’Souza, Jeevitha, Marisat, Monzer, Sprecher, Uri, Wald‐Altman, Shane, Dukhovny, Anna, Raviv, Yuval, Da’adoosh, Benny, Engel, Hamutal, Benhamron, Sandrine, Nitzan, Keren, Sweetat, Sahar, Permyakova, Anna, Mordechai, Anat, Akman, Hasan Orhan, Rosenmann, Hanna, Lossos, Alexander, Tam, Joseph, Minassian, Berge A., Weil, Miguel

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Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome von Hanein, Sylvain, Martin, Elodie, Boukhris, Amir, Byrne, Paula, Goizet, Cyril, Hamri, Abdelmadjid, Benomar, Ali, Lossos, Alexander, Denora, Paola, Fernandez, José, Elleuch, Nizar, Forlani, Sylvie, Durr, Alexandra, Feki, Imed, Hutchinson, Michael, Santorelli, Filippo M., Mhiri, Chokri, Brice, Alexis, Stevanin, Giovanni

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Structural basis of glycogen branching enzyme deficiency and pharmacologic rescue by rational peptide design von Froese, D Sean, Michaeli, Amit, McCorvie, Thomas J, Krojer, Tobias, Sasi, Meitav, Melaev, Esther, Goldblum, Amiram, Zatsepin, Maria, Lossos, Alexander, Álvarez, Rafael, Escribá, Pablo V, Minassian, Berge A, von Delft, Frank, Kakhlon, Or, Yue, Wyatt W

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Neurological misdiagnoses of lymphoma von Makranz, Chen, Arkadir, David, Nachmias, Boaz, Gatt, Moshe E., Eliahou, Ruth, Atlan, Karine, Mordechai, Anat, Goldshmit, Netta, Lossos, Alexander

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Triacylglycerol mimetics regulate membrane interactions of glycogen branching enzyme: implications for therapy von Alvarez, Rafael, Casas, Jesús, López, David J., Ibarguren, Maitane, Suari-Rivera, Ariadna, Terés, Silvia, Guardiola-Serrano, Francisca, Lossos, Alexander, Busquets, Xavier, Kakhlon, Or, Escribá, Pablo V.

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Adult polyglucosan body disease: Natural History and Key Magnetic Resonance Imaging Findings von Mochel, Fanny, Schiffmann, Raphael, Steenweg, Marjan E., Akman, Hasan O., Wallace, Mary, Sedel, Frédéric, Laforêt, Pascal, Levy, Richard, Powers, J. Michael, Demeret, Sophie, Maisonobe, Thierry, Froissart, Roseline, Da Nobrega, Bruno Barcelos, Fogel, Brent L., Natowicz, Marvin R., Lubetzki, Catherine, Durr, Alexandra, Brice, Alexis, Rosenmann, Hanna, Barash, Varda, Kakhlon, Or, Gomori, J. Moshe, van der Knaap, Marjo S., Lossos, Alexander

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KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations von KLEBEL, Stephan, LOSSOS, Alexander, RASTETTER, Agnes, MARTIN, Elodie, BOUTEILLER, Delphine, ORLANDO, Laurent, GYAPAY, Gabor, EL-HACHIMI, Khalid H, ZIMMERMAN, Batel, GAMLIEL, Moriya, MISK, Adel, LERER, Israela, AZZEDINE, Hamid, BRICE, Alexis, DURR, Alexandra, STEVANIN, Giovanni, MUNDWILLER, Emeline, SHEFFER, Ruth, GAUSSEN, Marion, MARELLI, Cecilia, NAWARA, Magdalena, CARPENTIER, Wassila, MEYER, Vincent

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Multi-system neurological disorder associated with a CRYAB variant von Sadeh, Menachem, Rahat, Dolev, Meiner, Vardiella, Fellig, Yakov, Arad, Michael, Schueler-Furman, Ora, Hu, Ying, Li, Yan, Bönnemann, Carsten G., Lossos, Alexander

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Clinical utility and treatment outcome of comprehensive genomic profiling in high grade glioma patients von Blumenthal, Deborah T., Dvir, Addie, Lossos, Alexander, Tzuk-Shina, Tzahala, Lior, Tzach, Limon, Dror, Yust-Katz, Shlomit, Lokiec, Alejandro, Ram, Zvi, Ross, Jeffrey S., Ali, Siraj M., Yair, Roi, Soussan-Gutman, Lior, Bokstein, Felix

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SCLC, Paraneoplastic Dermatomyositis, Positive Transcription Intermediary Factor 1-γ, and Point Mutation in the Transcription Intermediary Factor 1-γ Coding Gene: A Case Report von Arnon, Johnathan, Elia, Anna, Nevo, Yuval, Lossos, Alexander, Nechushtan, Hovav

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Diagnostic clues in herpes encephalitis following radiation therapy von Benoliel Berman, Tal, Bauer, Max, Moscovici, Samuel, Lossos, Alexander

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Prolonged Hiccups Following a Single Oral Dose of Prednisone von Lossos, Bar, Cherniak, Meir, Lossos, Alexander

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Teaching Neuro Images : Hypertrophic olivary degeneration in a young man with POLG gene mutation von Arkadir, David, Meiner, Vardiella, Karni, Arnon, Lossos, Alexander

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