Recombinant Adeno-Associated Virus Serotype 9 Gene Therapy in Spinal Muscular Atrophy

por Kotulska, Katarzyna, Fattal-Valevski, Aviva, Haberlova, Jana
Publicado 2021

Controlled amnioreduction for twin-to-twin transfusion syndrome

por Gordon, Zoya, Fattal-Valevski, Aviva, Elad, David, Jaffa, Ariel J.
Publicado 2022

Functional Benefit and Orthotic Effect of Dorsiflexion-FES in Children with Hemiplegic Cerebral Palsy

por Segal, Idan, Khamis, Sam, Sagie, Liora, Genizi, Jacob, Azriel, David, Katzenelenbogen, Sharona, Fattal-Valevski, Aviva
Publicado 2023

Cerebrospinal fluid characteristics of patients treated with intrathecal nusinersen for spinal muscular atrophy

por Orbach, Rotem, Sagi, Liora, Sadot, Efraim, Tokatly Latzer, Itay, Shtamler, Anna, Zisberg, Tehila, Fattal‐Valevski, Aviva
Publicado 2022

Radiologically isolated aquaporin-4 antibody neuromyelitis optica spectrum disorder

por Abdel-Mannan, Omar, Klein, Ainat, Bachar Zipori, Anat, Ben-Sira, Liat, Fattal-valevski, Aviva, Hacohen, Yael, Meirson, Hadas
Publicado 2022

Brain Plasticity following Intensive Bimanual Therapy in Children with Hemiparesis: Preliminary Evidence

por Weinstein, Maya, Myers, Vicki, Green, Dido, Schertz, Mitchell, Shiran, Shelly I., Geva, Ronny, Artzi, Moran, Gordon, Andrew M., Fattal-Valevski, Aviva, Ben Bashat, Dafna
Publicado 2015

Effect of cyclic, low dose pyrimethamine treatment in patients with Late Onset Tay Sachs: an open label, extended pilot study

por Osher, Etty, Fattal-Valevski, Aviva, Sagie, Liora, Urshanski, Nataly, Sagiv, Nadav, Peleg, Leah, Lerman-Sagie, Tally, Zimran, Ari, Elstein, Deborah, Navon, Ruth, Valevski, Avi, Stern, Naftali
Publicado 2015

Cortical Reorganization following Injury Early in Life

por Artzi, Moran, Shiran, Shelly Irene, Weinstein, Maya, Myers, Vicki, Tarrasch, Ricardo, Schertz, Mitchell, Fattal-Valevski, Aviva, Miller, Elka, Gordon, Andrew M., Green, Dido, Ben Bashat, Dafna
Publicado 2016

Muscle microRNAs in the cerebrospinal fluid predict clinical response to nusinersen therapy in type II and type III spinal muscular atrophy patients

por Magen, Iddo, Aharoni, Sharon, Yacovzada, Nancy Sarah, Tokatly Latzer, Itay, Alves, Christiano R. R., Sagi, Liora, Fattal‐Valevski, Aviva, Swoboda, Kathryn J., Katz, Jacob, Bruckheimer, Elchanan, Nevo, Yoram, Hornstein, Eran
Publicado 2022

ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia

por Bouwkamp, Christian G., Afawi, Zaid, Fattal-Valevski, Aviva, Krabbendam, Inge E., Rivetti, Stefano, Masalha, Rafik, Quadri, Marialuisa, Breedveld, Guido J., Mandel, Hanna, Tailakh, Muhammad Abu, Beverloo, H. Berna, Stevanin, Giovanni, Brice, Alexis, van IJcken, Wilfred F.J., Vernooij, Meike W., Dolga, Amalia M., de Vrij, Femke M.S., Bonifati, Vincenzo, Kushner, Steven A.
Publicado 2018

Thiamine deficiency disorders: diagnosis, prevalence, and a roadmap for global control programs

por Whitfield, Kyly C., Bourassa, Megan W., Adamolekun, Bola, Bergeron, Gilles, Bettendorff, Lucien, Brown, Kenneth H., Cox, Lorna, Fattal‐Valevski, Aviva, Fischer, Philip R., Frank, Elizabeth L., Hiffler, Laurent, Hlaing, Lwin Mar, Jefferds, Maria Elena, Kapner, Hallie, Kounnavong, Sengchanh, Mousavi, Maral P.S., Roth, Daniel E., Tsaloglou, Maria‐Nefeli, Wieringa, Frank, Combs, Gerald F.
Publicado 2018

Hereditary orotic aciduria identified by newborn screening

por Staretz-Chacham, Orna, Damseh, Nadirah S., Daas, Suha, Abu Salah, Nasser, Anikster, Yair, Barel, Ortal, Dumin, Elena, Fattal-Valevski, Aviva, Falik-Zaccai, Tzipora C., Hershkovitz, Eli, Josefsberg, Sagi, Landau, Yuval, Lerman-Sagie, Tally, Mandel, Hanna, Rock, Rachel, Rostami, Nira, Saraf-Levy, Talya, Shaul Lotan, Nava, Spiegel, Ronen, Tal, Galit, Ulanovsky, Igor, Wilnai, Yael, Korman, Stanley H., Almashanu, Shlomo
Publicado 2023

Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number

por Thompson, Kyle, Majd, Homa, Dallabona, Christina, Reinson, Karit, King, Martin S., Alston, Charlotte L., He, Langping, Lodi, Tiziana, Jones, Simon A., Fattal-Valevski, Aviva, Fraenkel, Nitay D., Saada, Ann, Haham, Alon, Isohanni, Pirjo, Vara, Roshni, Barbosa, Inês A., Simpson, Michael A., Deshpande, Charu, Puusepp, Sanna, Bonnen, Penelope E., Rodenburg, Richard J., Suomalainen, Anu, Õunap, Katrin, Elpeleg, Orly, Ferrero, Ileana, McFarland, Robert, Kunji, Edmund R.S., Taylor, Robert W.
Publicado 2016

Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number

por Thompson, Kyle, Majd, Homa, Dallabona, Cristina, Reinson, Karit, King, Martin S., Alston, Charlotte L., He, Langping, Lodi, Tiziana, Jones, Simon A., Fattal-Valevski, Aviva, Fraenkel, Nitay D., Saada, Ann, Haham, Alon, Isohanni, Pirjo, Vara, Roshni, Barbosa, Inês A., Simpson, Michael A., Deshpande, Charu, Puusepp, Sanna, Bonnen, Penelope E., Rodenburg, Richard J., Suomalainen, Anu, Õunap, Katrin, Elpeleg, Orly, Ferrero, Ileana, McFarland, Robert, Kunji, Edmund R.S., Taylor, Robert W.
Publicado 2016