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

por Elstein, Deborah, Zimran, Ari
Publicado 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 2009

Dental profile of patients with Gaucher disease

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

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 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 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 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 2015

Impact of the COVID-19 pandemic on the standard of care for patients with lysosomal storage diseases: A survey of healthcare professionals in the Fabry, Gaucher, and Hunter Outcome...

por Elstein, Deborah, Giugliani, Roberto, Muenzer, Joseph, Schenk, Jörn, Schwartz, Ida V.D., Anagnostopoulou, Christina
Publicado 2021

A global neuronopathic gaucher disease registry (GARDIAN): a patient-led initiative

por Collin-Histed, Tanya, Stoodley, Madeline, Beusterien, Kathleen, Elstein, Deborah, Jaffe, Dena H., Revel-Vilk, Shoshana, Davies, Elin Haf
Publicado 2023

FindZebra online search delving into rare disease case reports using natural language processing

por Liévin, Valentin, Hansen, Jonas Meinertz, Lund, Allan, Elstein, Deborah, Matthiesen, Mads Emil, Elomaa, Kaisa, Zarakowska, Kaja, Himmelhan, Iris, Botha, Jaco, Borgeskov, Hanne, Winther, Ole
Publicado 2023

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 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 2015

Demographics and patient characteristics of 1209 patients with Gaucher disease: Descriptive analysis from the Gaucher Outcome Survey (GOS)

por Zimran, Ari, Belmatoug, Nadia, Bembi, Bruno, Deegan, Patrick, Elstein, Deborah, Fernandez‐Sasso, Diego, Giraldo, Pilar, Goker‐Alpan, Ozlem, Lau, Heather, Lukina, Elena, Panahloo, Zoya, Schwartz, Ida Vanessa D.
Publicado 2017

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 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 2013

Development and validation of Gaucher disease type 1 (GD1)-specific patient-reported outcome measures (PROMs) for clinical monitoring and for clinical trials

por Elstein, Deborah, Belmatoug, Nadia, Deegan, Patrick, Göker-Alpan, Özlem, Hughes, Derralynn A., Schwartz, Ida Vanessa D., Weinreb, Neal, Bonner, Nicola, Panter, Charlotte, Fountain, Donna, Lenny, Andrew, Longworth, Louise, Miller, Rachael, Shah, Koonal, Schenk, Jörn, Sen, Rohini, Zimran, Ari
Publicado 2022

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 2013