Gaucher disease and the clinical experience with substrate reduction therapy.

Por Zimran, Ari, Elstein, Deborah
Publicado em 2003

Review of the safety and efficacy of imiglucerase treatment of Gaucher disease

Por Elstein, Deborah, Zimran, Ari
Publicado em 2009

Poor results of drilling in early stages of juxta-articular osteonecrosis in 12 joints affected by Gaucher disease

Por Lebel, Ehud, Phillips, Mici, Elstein, Deborah, Zimran, Ari, Itzchaki, Menachem
Publicado em 2009

Dental profile of patients with Gaucher disease

Por Mann Jonathan, Sgan-Cohen Harold, Elstein Deborah, Fischman Stuart L, Zimran Ari
Publicado em 2003-07-01

Dental profile of patients with Gaucher disease

Por Fischman, Stuart L, Elstein, Deborah, Sgan-Cohen, Harold, Mann, Jonathan, Zimran, Ari
Publicado em 2003

Mandibular and Dental Manifestations of Gaucher Disease

Por Saranjam, Hamid R., Sidransky, Ellen, Levine, William Z., Zimran, Ari, Elstein, Deborah
Publicado em 2012

Bone Mineral Density in Gravida: Effect of Pregnancies and Breast-Feeding in Women of Differing Ages and Parity

Por Lebel, Ehud, Mishukov, Yuri, Babchenko, Liana, Samueloff, Arnon, Zimran, Ari, Elstein, Deborah
Publicado no J Osteoporos (2014)

Achievement of Therapeutic Goals with Low-Dose Imiglucerase in Gaucher Disease: A Single-Center Experience

Por Tukan, Irina, Hadas-Halpern, Irith, Altarescu, Gheona, Abrahamov, Ayala, Elstein, Deborah, Zimran, Ari
Publicado em 2013

Anesthetic management for oocyte retrieval: An exploratory analysis comparing outcome in in vitro fertilization cycles with and without pre-implantation genetic diagnosis

Por Ioscovich, Alexander, Eldar-Geva, Talia, Weitman, Marina, Altarescu, Gheona, Rivilis, Alina, Elstein, Deborah
Publicado em 2013

Seven‐year safety and efficacy with velaglucerase alfa for treatment‐naïve adult patients with type 1 Gaucher disease

Por Zimran, Ari, Wang, Nan, Ogg, Carol, Crombez, Eric, Cohn, Gabriel M., Elstein, Deborah
Publicado no Am J Hematol (2015)

Prevention of Lysosomal Storage Diseases and Derivation of Mutant Stem Cell Lines by Preimplantation Genetic Diagnosis

Por Altarescu, Gheona, Beeri, Rachel, Eiges, Rachel, Epsztejn-Litman, Silvina, Eldar-Geva, Talia, Elstein, Deborah, Zimran, Ari, Margalioth, Ehud J., Levy-Lahad, Ephrat, Renbaum, Paul
Publicado em 2012

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 no Orphanet J Rare Dis (2015)

Proof-of-principle rapid noninvasive prenatal diagnosis of autosomal recessive founder mutations

Por Zeevi, David A., Altarescu, Gheona, Weinberg-Shukron, Ariella, Zahdeh, Fouad, Dinur, Tama, Chicco, Gaya, Herskovitz, Yair, Renbaum, Paul, Elstein, Deborah, Levy-Lahad, Ephrat, Rolfs, Arndt, Zimran, Ari
Publicado no J Clin Invest (2015)

Velaglucerase alfa (VPRIV) enzyme replacement therapy in patients with Gaucher disease: Long-term data from phase III clinical trials

Por Hughes, Derralynn A, Gonzalez, Derlis E, Lukina, Elena A, Mehta, Atul, Kabra, Madhulika, Elstein, Deborah, Kisinovsky, Isaac, Giraldo, Pilar, Bavdekar, Ashish, Hangartner, Thomas N, Wang, Nan, Crombez, Eric, Zimran, Ari
Publicado no Am J Hematol (2015)

Glucosylsphingosine Is a Highly Sensitive and Specific Biomarker for Primary Diagnostic and Follow-Up Monitoring in Gaucher Disease in a Non-Jewish, Caucasian Cohort of Gaucher Dis...

Por Rolfs, Arndt, Giese, Anne-Katrin, Grittner, Ulrike, Mascher, Daniel, Elstein, Deborah, Zimran, Ari, Böttcher, Tobias, Lukas, Jan, Hübner, Rayk, Gölnitz, Uta, Röhle, Anja, Dudesek, Ales, Meyer, Wolfgang, Wittstock, Matthias, Mascher, Hermann
Publicado em 2013

Comparison of Parkinson risk in Ashkenazi Jewish Gaucher patients and GBA heterozygotes

Por Alcalay, Roy N., Dinur, Tama, Quinn, Timothy, Sakanaka, Karina, Levy, Oren, Waters, Cheryl, Fahn, Stanley, Dorovski, Tsvyatko, Chung, Wendy K, Pauciulo, Michael, Nichols, William, Rana, Huma Q., Balwani, Manisha, Bier, Louise, Elstein, Deborah, Zimran, Ari
Publicado em 2014

Functional and genetic characterization of the non-lysosomal glucosylceramidase 2 as a modifier for Gaucher disease

Por Yildiz, Yildiz, Hoffmann, Per, vom Dahl, Stefan, Breiden, Bernadette, Sandhoff, Roger, Niederau, Claus, Horwitz, Mia, Karlsson, Stefan, Filocamo, Mirella, Elstein, Deborah, Beck, Michael, Sandhoff, Konrad, Mengel, Eugen, Gonzalez, Maria C, Nöthen, Markus M, Sidransky, Ellen, Zimran, Ari, Mattheisen, Manuel
Publicado em 2013

Safety and efficacy of velaglucerase alfa in Gaucher disease type 1 patients previously treated with imiglucerase

Por Zimran, Ari, Pastores, Gregory M., Tylki-Szymanska, Anna, Hughes, Derralynn A., Elstein, Deborah, Mardach, Rebecca, Eng, Christine, Smith, Laurie, Heisel-Kurth, Margaret, Charrow, Joel, Harmatz, Paul, Fernhoff, Paul, Rhead, William, Longo, Nicola, Giraldo, Pilar, Ruiz, Juan A., Zahrieh, David, Crombez, Eric, Grabowski, Gregory A.
Publicado em 2013

Zimran A, Brill-Almon E, Chertkoff R, et al. Pivotal trial with plant cell–expressed recombinant glucocerebrosidase, taliglucerase alfa, a novel enzyme replacement therapy for Gauc...

Por Zimran, Ari, Brill-Almon, Einat, Chertkoff, Raul, Petakov, Milan, Blanco-Favela, Francisco, Muñoz, Eduardo Terreros, Solorio-Meza, Sergio E., Amato, Dominick, Duran, Gloria, Giona, Fiorina, Heitner, Rene, Rosenbaum, Hanna, Giraldo, Pilar, Mehta, Atul, Park, Glen, Phillips, Mici, Elstein, Deborah, Altarescu, Gheona, Szleifer, Mali, Hashmueli, Sharon, Aviezer, David
Publicado em 2012