Zobrazeno 1 - 10
of 837
pro vyhledávání: '"A. Fattal-Valevski"'
Autor:
Esther Osher, Yossi Anis, Ruth Singer-Shapiro, Nataly Urshanski, Tamar Unger, Shira Albeck, Oren Bogin, Gary Weisinger, Fortune Kohen, Avi Valevski, Aviva Fattal-Valevski, Liora Sagi, Michal Weitman, Yulia Shenberger, Nadav Sagiv, Ruth Navon, Meir Wilchek, Naftali Stern
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 32, Iss 3, Pp 101300- (2024)
Tay-Sachs (TS) disease is a neurodegenerative disease resulting from mutations in the gene encoding the α-subunit (HEXA) of lysosomal β-hexosaminidase A (HexA). We report that (1) recombinant HEXA alone increased HexA activity and decreased GM2 con
Externí odkaz:
https://doaj.org/article/b46b268575554f2eb291b7d475a23c94
Autor:
Osher, Esther, Anis, Yossi, Singer-Shapiro, Ruth, Urshanski, Nataly, Unger, Tamar, Albeck, Shira, Bogin, Oren, Weisinger, Gary, Kohen, Fortune, Valevski, Avi, Fattal-Valevski, Aviva, Sagi, Liora, Weitman, Michal, Shenberger, Yulia, Sagiv, Nadav, Navon, Ruth, Wilchek, Meir, Stern, Naftali
Publikováno v:
In Molecular Therapy - Methods & Clinical Development 12 September 2024 32(3)
Autor:
Kirschner, Janbernd, Bernert, Günther, Butoianu, Nina, De Waele, Liesbeth, Fattal-Valevski, Aviva, Haberlova, Jana, Moreno, Teresa, Klein, Andrea, Kostera-Pruszczyk, Anna, Mercuri, Eugenio, Quijano-Roy, Susana, Sejersen, Thomas, Tizzano, Eduardo F., van der Pol, W Ludo, Wallace, Sean, Zafeiriou, Dimitrios, Ziegler, Andreas, Muntoni, Francesco, Servais, Laurent
Publikováno v:
In European Journal of Paediatric Neurology July 2024 51:73-78
Autor:
Kurd, Mohammad, Pratt, Li-tal, Gilboa, Tal, Fattal-valevski, Aviva, Vaknin-Dembinsky, Adi, Gadoth, Avi, Hacohen, Yael, Meirson, Hadas
Publikováno v:
In European Journal of Paediatric Neurology March 2024 49:13-16
Akademický článek
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Autor:
Zerem, Ayelet, Libzon, Stephanie, Ben Sira, Liat, Meirson, Hadas, Hausman-Kedem, Moran, Haviv, Noam, Yosovich, Keren, Mory, Adi, Baris Feldman, Hagit, Lev, Dorit, Lerman-Sagie, Tally, Fattal-Valevski, Aviva, Hacohen, Yael, Marom, Daphna
Publikováno v:
In European Journal of Paediatric Neurology July 2023 45:29-35
Autor:
Tokatly Latzer, Itay, Tauman, Riva, Senderowich, Noam, Markovitz, Raviv, Bachar-Zipori, Anat, Klein, Ainat, Meirson, Hadas, Fattal-Valevski, Aviva, Hausman-Kedem, Moran
Publikováno v:
In Pediatric Neurology May 2023 142:39-46
Autor:
Orna Staretz-Chacham, Nadirah S. Damseh, Suha Daas, Nasser Abu Salah, Yair Anikster, Ortal Barel, Elena Dumin, Aviva Fattal-Valevski, Tzipora C. Falik-Zaccai, Eli Hershkovitz, Sagi Josefsberg, Yuval Landau, Tally Lerman-Sagie, Hanna Mandel, Rachel Rock, Nira Rostami, Talya Saraf-Levy, Nava Shaul Lotan, Ronen Spiegel, Galit Tal, Igor Ulanovsky, Yael Wilnai, Stanley H. Korman, Shlomo Almashanu
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Introduction: Hereditary orotic aciduria is an extremely rare, autosomal recessive disease caused by deficiency of uridine monophosphate synthase. Untreated, affected individuals may develop refractory megaloblastic anemia, neurodevelopmental disabil
Externí odkaz:
https://doaj.org/article/a4eeec32a8884c4395e424f817425fe1
Autor:
Menascu, Shay, Fattal-Valevski, Aviva, Vaknin-Dembinsky, Adi, Milo, Ron, Geva, Keren, Magalashvili, David, Dolev, Mark, Flecther, Shlomo, Kalron, Alon, Miron, Shmulik, Hoffmann, Chen, Aloni, Roy, Gurevich, Michael, Achiron, Anat
Publikováno v:
In Journal of the Neurological Sciences 15 January 2022 432
Autor:
Fattal-Valevski, Aviva, Ben Sira, Liat, Lerman-Sagie, Tally, Strausberg, Rachel, Bloch-Mimouni, Aviva, Edvardson, Simon, Kaufman, Rami, Chernuha, Veronika, Schneebaum Sender, Nira, Heimer, Gali, Ben Zeev, Bruria
Publikováno v:
In European Journal of Paediatric Neurology May 2021 32:40-45