Tonic-clonic seizures in patients taking sildenafil

par Gilad, Ronit, Lampl, Yair, Eshel, Yehiel, Sadeh, Menachem
Publié 2002

BENEFICIAL EFFECT OF ALBUTEROL IN CONGENTIAL MYASTHENIC SYNDROME WITH EPSILON SUBUINT MUTATIONS

par Sadeh, Menachem, Shen, Xin-Ming, Engel, Andrew G.
Publié 2011

Clinical, epidemiological, genetic, and electrophysiological characteristics of transthyretin familial amyloid polyneuropathies in Israel

par Sadeh, Menachem, Livneh, Avi, Arad, Michael, Lossos, Alexander
Publié dans Orphanet J Rare Dis (2015)

Electrical stimulation of the posterior tibial nerve reduces neuropathic pain in patients with polyneuropathy

par Dabby, Ron, Sadeh, Menachem, Goldberg, Ilan, Finkelshtein, Vitaly
Publié dans J Pain Res (2017)

Auditory Hallucinations in Acute Stroke

par Lampl, Yair, Lorberboym, Mordechai, Gilad, Ronit, Boaz, Mona, Sadeh, Menachem
Publié dans Behav Neurol (2005)

Pathological Laughter as a Symptom of Midbrain Infarction

par Dabby, Ron, Watemberg, Nathan, Lampl, Yair, Eilam, Anda, Rapaport, Abraham, Sadeh, Menachem
Publié dans Behav Neurol (2004)

The Proteomic Profile of Hereditary Inclusion Body Myopathy

par Sela, Ilan, Milman Krentsis, Irit, Shlomai, Zipora, Sadeh, Menachem, Dabby, Ron, Argov, Zohar, Ben-Bassat, Hannah, Mitrani-Rosenbaum, Stella
Publié 2011

Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama Disease

par Blumen, Sergiu C., Drory, Vivian E., Sadeh, Menachem, El-Ad, Baruch, Soimu, Uri, Groozman, Galina B., Bouchard, Jean-Pierre, Goldfarb, Lev G.
Publié 2010

Two novel MYH7 proline substitutions cause Laing Distal Myopathy-like phenotypes with variable expressivity and neck extensor contracture

par Feinstein-Linial, Miora, Buvoli, Massimo, Buvoli, Ada, Sadeh, Menachem, Dabby, Ron, Straussberg, Rachel, Shelef, Ilan, Dayan, Daniel, Leinwand, Leslie Anne, Birk, Ohad S.
Publié dans BMC Med Genet (2016)

Congenital myasthenic syndrome in Israel: Genetic and clinical characterization

par Aharoni, Sharon, Sadeh, Menachem, Shapira, Yehuda, Edvardson, Simon, Daana, Muhannad, Dor-Wollman, Talia, Mimouni-Bloch, Aviva, Halevy, Ayelet, Cohen, Rony, Sagie, Liora, Argov, Zohar, Rabie, Malcolm, Spiegel, Ronen, Chervinsky, Ilana, Orenstein, Naama, Engel, Andrew G., Nevo, Yoram
Publié dans Neuromuscul Disord (2016)

Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosis

par González-Pérez, Paloma, Cirulli, Elizabeth T., Drory, Vivian E., Dabby, Ron, Nisipeanu, Puiu, Carasso, Ralph L., Sadeh, Menachem, Fox, Andrew, Festoff, Barry W., Sapp, Peter C., McKenna-Yasek, Diane, Goldstein, David B., Brown, Robert H., Blumen, Sergiu C.
Publié 2012