Quantitative sonographic assessment of muscle thickness and fasciculations distribution is a sensitive tool for neuromuscular disorders

by Abraham, Alon, Fainmesser, Yaara, Drory, Vivian E, Bril, Vera
Published in PloS one

Influence of serum uric acid levels on prognosis and survival in amyotrophic lateral sclerosis: a meta-analysis

by Abraham, Alon, Drory, Vivian E.
Published in Journal of neurology

Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis

by WU, Chi-Hong, FALLINI, Claudia, KOST, Jason E, GONZALEZ-PEREZ, Paloma, FOX, Andrew D, ADAMS, Jenni, TARONI, Franco, TILOCA, Cinzia, LYN LECLERC, Ashley, CHAFE, Shawn C, MANGROO, Dev, MOORE, Melissa J, TICOZZI, Nicola, ZITZEWITZ, Jill A, XU, Zuo-Shang, DEN BERG, Leonard H. Van, GLASS, Jonathan D, SICILIANO, Gabriele, CIRULLI, Elizabeth T, GOLDSTEIN, David B, SALACHAS, Francois, MEININGER, Vincent, ROSSOLL, Wilfried, KEAGLE, Pamela J, RATTI, Antonia, GELLERA, Cinzia, BOSCO, Daryl A, BASSELL, Gary J, SILANI, Vincenzo, DRORY, Vivian E, BROWN, Robert H, LANDERS, John E, SAPP, Peter C, PIOTROWSKA, Katarzyna, LOWE, Patrick, KOPPERS, Max, MCKENNA-YASEK, Diane, BARON, Desiree M
Published in Nature (London)

Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis

by Johnson, Janel O, Glynn, Shannon M, Gibbs, J Raphael, Nalls, Mike A, Sabatelli, Mario, Restagno, Gabriella, Drory, Vivian E, Chiò, Adriano, Rogaeva, Ekaterina, Traynor, Bryan J
Published in Brain (London, England : 1878)

Wet, volatile, and dry biomarkers of exercise-induced muscle fatigue

by Finsterer, Josef, Drory, Vivian E
Published in BMC musculoskeletal disorders

Mechanism, Prevalence, and More Severe Neuropathy Phenotype of the Charcot-Marie-Tooth Type 1A Triplication

by Liu, Pengfei, Gelowani, Violet, Zhang, Feng, Drory, Vivian E., Ben-Shachar, Shay, Roney, Erin, Medeiros, Adam C., Moore, Rebecca J., DiVincenzo, Christina, Burnette, William B., Higgins, Joseph J., Li, Jun, Orr-Urtreger, Avi, Lupski, James R.
Published in American journal of human genetics

Glycans in sera of amyotrophic lateral sclerosis patients and their role in killing neuronal cells

by Edri-Brami, Meital, Rosental, Benyamin, Hayoun, Dana, Welt, Michael, Rosen, Hila, Wirguin, Itzhak, Nefussy, Beatrice, Drory, Vivian E, Porgador, Angel, Lichtenstein, Rachel G
Published in PloS one

Split-hand phenomenon in motor neuron diseases: Sonographic assesment of muscle thickness

by Abraham, Alon, Fainmesser, Yaara, Drory, Vivian E, Bril, Vera
Published in Clinical neurophysiology

Superiority of sonographic evaluation of contracted versus relaxed muscle thickness in motor neuron diseases

by Abraham, Alon, Fainmesser, Yaara, Lovblom, Leif E., Bril, Vera, Drory, Vivian E
Published in Clinical neurophysiology

The Sensitivity and Specificity of Split-Hand Index Using Muscle Sonography

by Avidan, Reuven, Fainmesser, Yaara, Drory, Vivian E., Bril, Vera, Abraham, Alon
Published in Canadian journal of neurological sciences

Longer-term follow-up of nusinersen efficacy and safety in adult patients with spinal muscular atrophy types 2 and 3

by Fainmesser, Yaara, Drory, Vivian E, Ben-Shushan, Stephan, Lavon, Anat, Spector, Luba, Abramovich, Beatrice, Abraham, Alon
Published in Neuromuscular disorders : NMD

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

by Johnson, Janel O, Pioro, Erik P, Boehringer, Ashley, Chia, Ruth, Feit, Howard, Renton, Alan E, Pliner, Hannah A, Abramzon, Yevgeniya, Marangi, Giuseppe, Winborn, Brett J, Gibbs, J Raphael, Nalls, Michael A, Morgan, Sarah, Shoai, Maryam, Hardy, John, Pittman, Alan, Orrell, Richard W, Malaspina, Andrea, Sidle, Katie C, Fratta, Pietro, Harms, Matthew B, Baloh, Robert H, Pestronk, Alan, Weihl, Conrad C, Rogaeva, Ekaterina, Zinman, Lorne, Drory, Vivian E, Borghero, Giuseppe, Mora, Gabriele, Calvo, Andrea, Rothstein, Jeffrey D, Drepper, Carsten, Sendtner, Michael, Singleton, Andrew B, Taylor, J Paul, Cookson, Mark R, Restagno, Gabriella, Sabatelli, Mario, Bowser, Robert, Chiò, Adriano, Traynor, Bryan J
Published in Nature neuroscience

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

by Majounie, Elisa, PhD, Renton, Alan E, PhD, Mok, Kin, MSc, Dopper, Elise GP, Waite, Adrian, PhD, Rollinson, Sara, PhD, Chiò, Adriano, MD, Restagno, Gabriella, MD, Nicolaou, Nayia, MSc, Simon-Sanchez, Javier, PhD, van Swieten, John C, Prof, Abramzon, Yevgeniya, Johnson, Janel O, PhD, Sendtner, Michael, Prof, Pamphlett, Roger, MD, Orrell, Richard W, MD, Mead, Simon, MD, Sidle, Katie C, MD, Houlden, Henry, Prof, Rohrer, Jonathan D, MD, Morrison, Karen E, Prof, Pall, Hardev, MD, Talbot, Kevin, Prof, Ansorge, Olaf, MD, Hernandez, Dena G, MSc, Arepalli, Sampath, MS, Sabatelli, Mario, MD, Mora, Gabriele, MD, Corbo, Massimo, MD, Giannini, Fabio, MD, Calvo, Andrea, MD, Englund, Elisabet, MD, Borghero, Giuseppe, MD, Floris, Gian Luca, MD, Remes, Anne M, Prof, Laaksovirta, Hannu, MD, McCluskey, Leo, MD, Trojanowski, John Q, Prof, Van Deerlin, Vivianna M, MD, Schellenberg, Gerard D, Prof, Nalls, Michael A, PhD, Drory, Vivian E, MD, Lu, Chin-Song, Prof, Yeh, Tu-Hsueh, MD, Ishiura, Hiroyuki, MD, Takahashi, Yuji, MD, Tsuji, Shoji, Prof, Le Ber, Isabelle, MD, Brice, Alexis, Prof, Drepper, Carsten, PhD, Williams, Nigel, PhD, Kirby, Janine, PhD, Shaw, Pamela, Prof, Hardy, John, Prof, Tienari, Pentti J, MD, Heutink, Peter, Prof, Morris, Huw R, MD, Pickering-Brown, Stuart, Prof, Traynor, Bryan J, Dr
Published in Lancet neurology

Characterization of patients with ocular myasthenia gravis — A case series

by Karni, Arnon, Asmail, Ali, Drory, Vivian E., Kolb, Hadar, Kesler, Anat
Published in eNeurologicalSci

Pre-morbid Laboratory Tests, Diseases, and Medications in Amyotrophic Lateral Sclerosis in Israel

by Abraham, Alon, Abramovich, Beatrice, Banon, Tamar, Weil, Clara, Chodick, Gabriel, Birman, Nurit, Fainmesser, Yaara, Drory, Vivian E
Published in The Israel Medical Association journal

Common genetic basis of ALS patients and soccer players may contribute to disease risk

by Ben-Zaken, Sigal, Nefussy, Beatrice, Meckel, Yoav, Eliakim, Alon, Nemet, Dan, Gotkine, Marc, Lorber, Dana, Zeev, Aviva, Drory, Vivian E.
Published in Neurological sciences

Rare homozygosity in amyotrophic lateral sclerosis suggests the contribution of recessive variants to disease genetics

by Goldstein, Orly, Kedmi, Merav, Gana-Weisz, Mali, Twito, Shir, Nefussy, Beatrice, Vainer, Batel, Fainmesser, Yaara, Abraham, Alon, Nayshool, Omri, Orr-Urtreger, Avi, Drory, Vivian E.
Published in Journal of the neurological sciences

Effect of ethnic origin and gender on the clinical manifestations of myasthenia gravis among the Jewish population in Israel

by Asmail, Ali, Kesler, Anat, Drory, Vivian E, Kolb, Hadar, Karni, Arnon
Published in Journal of neuroimmunology

Thymus involvement in myasthenia gravis: Epidemiological and clinical impacts of different self-tolerance breakdown mechanisms

by Karni, Arnon, Asmail, Ali, Drory, Vivian E, Kolb, Hadar, Kesler, Anat
Published in Journal of neuroimmunology

Do patients with amyotrophic lateral sclerosis (ALS) have increased energy needs?

by Vaisman, Nachum, Lusaus, Michal, Nefussy, Beatrice, Niv, Eva, Comaneshter, Doron, Hallack, Ron, Drory, Vivian E
Published in Journal of the neurological sciences