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Your search keyword '"Mozer‐Glassberg, Yael"' showing total 8 results
Start Over Author "Mozer‐Glassberg, Yael" Publisher elsevier b.v.
8 results on '"Mozer‐Glassberg, Yael"'

1. Cell-based BSEP trans-inhibition: A novel, non-invasive test for diagnosis of antibody-induced BSEP deficiency

Author

Stindt, Jan, Dröge, Carola, Lainka, Elke, Kathemann, Simone, Pfister, Eva-Doreen, Baumann, Ulrich, Stalke, Amelie, Grabhorn, Enke, Shagrani, Mohammad Ali, Mozer-Glassberg, Yael, Hartley, Jane, Wammers, Marianne, Klindt, Caroline, Philippski, Paulina, Liebe, Roman, Herebian, Diran, Mayatepek, Ertan, Berg, Thomas, Schmidt-Choudhury, Anjona, Wiek, Constanze, Hanenberg, Helmut, Luedde, Tom, and Keitel, Verena

Published
2023
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2. Genotype correlates with the natural history of severe bile salt export pump deficiency

Author

van Wessel, Daan B.E., Thompson, Richard J., Gonzales, Emmanuel, Jankowska, Irena, Sokal, Etienne, Grammatikopoulos, Tassos, Kadaristiana, Agustina, Jacquemin, Emmanuel, Spraul, Anne, Lipiński, Patryk, Czubkowski, Piotr, Rock, Nathalie, Shagrani, Mohammad, Broering, Dieter, Algoufi, Talal, Mazhar, Nejat, Nicastro, Emanuele, Kelly, Deirdre A., Nebbia, Gabriella, Arnell, Henrik, Björn Fischler, Hulscher, Jan B.F., Serranti, Daniele, Arikan, Cigdem, Polat, Esra, Debray, Dominique, Lacaille, Florence, Goncalves, Cristina, Hierro, Loreto, Muñoz Bartolo, Gema, Mozer-Glassberg, Yael, Azaz, Amer, Brecelj, Jernej, Dezsőfi, Antal, Calvo, Pier Luigi, Grabhorn, Enke, Sturm, Ekkehard, van der Woerd, Wendy J., Kamath, Binita M., Wang, Jian-She, Li, Liting, Durmaz, Özlem, Onal, Zerrin, Bunt, Ton M.G., Hansen, Bettina E., and Verkade, Henkjan J.

Published
2020
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3. THU-289 - Analysis of long-term treatment effects of odevixibat on clinical outcomes in children with progressive familial intrahepatic cholestasis in odevixibat clinical studies vs external controls from the NAPPED database

Author

Hansen, Bettina, Valcheva, Velichka, Yu, Qifeng, van Wessel, Daan, Thompson, Richard, Gonzalès, Emmanuel, Jankowska, Irena, Sokal, Etienne, Grammatikopoulos, Tassos, Kadaristiana, Agustina, Jacquemin, Emmanuel, Spraul, Anne, Lipiński, Patryk, Czubkowski, Piotr, Rock, Nathalie, Shagrani, Mohammad, Kumar, Kishwer, Alkuraya, Fowzan, Sateesh, Meddirevula, Broering, Dieter Clemens, Nicastro, Emanuele, Kelly, Deirdre, Nebbia, Gabriella, Arnell, Henrik, Fischler, Björn, Serranti, Daniele, Arıkan, Cigdem, Polat, Esra, Debray, Dominique, Lacaille, Florence, Gonçalves, Cristina, Llanillo, Loreto Hierro, Bartolo, Gema Muñoz, Mozer-Glassberg, Yael, Azaz, Amer, Brecelj, Jernej, Dezsőfi, Antal, Calvo, Pier Luigi, Grabhorn, Enke, Sturm, Ekkehard, van der Woerd, Wendy L., Kamath, Binita M., Wang, Jian-She, Liting, Li, Durmaz, Ozlem, Önal, Zerrin, Felzen, Antonia, Nomden, Mark, Sonajalg, Jaak, Stein, Philip, Ni, Quanhong, Clemson, Christine, Mattsson, Jan, and Verkade, Henkjan J.

Published
2023
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4. Two decades of pediatric celiac disease in a tertiary referral center: What has changed?

Author

Krauthammer, Alexander, Guz-Mark, Anat, Zevit, Noam, Marderfeld, Luba, Waisbourd-Zinman, Orith, Silbermintz, Ari, Mozer-Glassberg, Yael, Nachmias Friedler, Vered, Rozenfeld Bar Lev, Michal, Matar, Manar, Assa, Amit, and Shamir, Raanan

Abstract

Celiac disease (CD) is common worldwide with increasing prevalence and changing presentation. To evaluate changes in the presentation and management of CD over the last two decades. Retrospective chart review of pediatric patients with CD between 01.1999 to 12.2018 was performed. Comparisons were made between an early (1999 to 2008) and late (2009 to 2018) decade, regarding clinical and laboratory parameters at presentation and follow-up. In a cohort of 932 patients (early decade n = 316, late decade n = 616), patients from the late decade presented with lower rates of weight loss and abdominal distention (24.2% vs 34.7% and 6% vs 11%, respectively p < 0.01), and with higher rates of abdominal pain or asymptomatic presentation (41.4% vs 27.4%, p < 0.01, and 18% vs 13%, p < 0.05, respectively). Good adherence to gluten-free diet was reported more often in the late decade (64% vs 50.6%, p < 0.001), and fewer patients were lost to follow-up. During the late decade, significantly higher rates of celiac serology normalization were achieved during the first two years of follow-up. In recent years, children with CD were diagnosed with milder symptoms, showed better adherence and demonstrated earlier normalization of celiac serology. [ABSTRACT FROM AUTHOR]

Published
2020
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5. FRI-436-Congenital porto-systemic shunts in children: Preliminary results from the IRCPSS

Author

McLin, Valérie, Franchi-Abella, Stéphanie, Debray, Dominique, Korff, Simona, Casotti, Valeria, Colledan, Michele, D’Antiga, Lorenzo, Goyet, Jean De Ville De, Durmaz, Ozlem, Lurz, Ebehard, Hierro, Loreto, Kanavaki, Ino, Lipsich, José, Lopez-Santamaria, Maria, Maria, Magnusson, Mozer-Glassberg, Yael, Ponce, Md, Pop, Tudor, Prieto, Cr, Rock, Nathalie, Stephenne, Xavier, Varma, Sharat, Wildhaber, Barbara, Guerin, Florent, and Gonzales, Emmanuel

Published
2019
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6. PS-195-Predicting long-term outcome after surgical biliary diversion in Bsep-deficiency patients: Results from the NAPPED consortium

Author

Wessel, Daan van, Thompson, Richard, Grammatikopoulos, Tassos, Kadaristiana, Agustina, Jankowska, Irena, Lipiński, Patryk, Czubkowski, Piotr, Gonzales, Emmanuel, Jacquemin, Emmanuel, Spraul, Anne, Sokal, Etienne, Shagrani, Mohammad Ali, Broering, Dieter Clemens, Algoufi, Talal, Mazhar, Nejat, Nicastro, Emanuele, Kelly, Deirdre, Nebbia, Gabriella, Arnell, Henrik, Fischler, Björn, Hulscher, JBF, Serranti, Daniele, Arıkan, Cigdem, Polat, Esra, Debray, Dominique, Lacaille, Florence, Gonçalves, Cristina, Hierro, Loreto, Bartolo, Gema Muñoz, Mozer-Glassberg, Yael, Azaz, Amer, Brecelj, Jernej, Dezsőfi, Antal, Calvo, Pier Luigi, Grabhorn, Enke, Sturm, Ekkehard, Woerd, Wendy van der, Kamath, Binita M., Wang, Jian-She, Liting, Li, Durmaz, Ozlem, Hansen, Bettina, and Verkade, Henkjan

Published
2019
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7. Imaging features of primary hyperoxaluria.

Author

Rootman, Mika Shapira, Mozer-Glassberg, Yael, Gurevich, Michael, Schwartz, Michael, and Konen, Osnat

Subjects
*MEDICAL imaging systems, *GENETIC disorders, *OXALATES, *KIDNEY transplantation, *KIDNEY calcification
Abstract

Abstract Primary hyperoxaluria (PH) is a group of autosomal recessive diseases that affect the metabolism of glyoxalate and oxalate. As a result of the enzymatic deficiency, there is overproduction and urinary excretion of oxalate with progressive renal damage and subsequent deposition of oxalate salts in various tissues. The definitive treatment in cases of end-stage kidney disease is a combined liver and kidney transplant. Imaging features are diverse and reflect the multiple organs that might be affected. These include nephrolithiasis and nephrocalcinosis, oxalate osteopathy, as well as other findings, such as splenomegaly and oxalate deposition in the heart. In this review article, we present various imaging findings that may appear in patients with PH. Highlights • Provide an overview of primary hyperoxaluria. • Describe the diverse imaging features of patients with primary hyperoxaluria. [ABSTRACT FROM AUTHOR]

Published
2018
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8. Evolution of disease phenotype in pediatric-onset Crohn’s disease after more than 10 years follow up—Cohort study.

Author

Rinawi, Firas, Assa, Amit, Hartman, Corina, Mozer Glassberg, Yael, Nachmias Friedler, Vered, Rosenbach, Yoram, Silbermintz, Ari, Zevit, Noam, and Shamir, Raanan

Abstract

Background Pediatric-onset Crohn’s disease (CD) is a heterogeneous disorder which is subjected to progression and complications in a substantial proportion of patients. Aims We aimed to assess the progression in pediatric-onset CD phenotype on long term follow up. Methods Medical charts of pediatric onset CD patients with at least 10 years follow-up were analyzed retrospectively. Disease phenotype was determined at diagnosis and during follow up at different time points. Phenotype was determined according to the Paris classification. The impact of possible predictors on phenotype progression was assessed as well as the association between different therapeutic regimens during disease course and phenotype progression. Results Progression of disease location, behavior, and perianal involvement was observed in 20%, 38% and 20% of patients, respectively, after a median follow-up of 16.4 (±4.4) years. Microscopic ileocolonic disease at diagnosis was significant predictors for progression of disease extent. Treatment with anti tumor necrosis factor-ɑ agents and number of flares per years of follow-up were associated with progression of disease extent, behavior and perianal involvement. Conclusion Disease extent, behavior and prevalence of perianal disease change significantly over time in pediatric-onset CD. In our cohort, most clinical, laboratory and endoscopic parameters do not serve as predictors for long-term disease progression. [ABSTRACT FROM AUTHOR]

Published
2016
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