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Elsevier电子期刊(76)

在“Elsevier电子期刊”中，命中：76条，耗时：小于0.01 秒

在所有数据库中总计命中：76条

1.Long-term hematological, visceral, and growth outcomes in children with Gaucher disease type 3 treated with imiglucerase in the International Collaborative Gaucher Group Gaucher Registry

作者：Amal El-Beshlawy^a ; Anna Tylki-Szymanska^b ; Ashok Vellodi^c ; Nadia Belmatoug^d ; Gregory A. Grabowski^e ; ^f ; Edwin H. Kolodny^g ; Julie L. Batista^h ; Gerald F. Coxⁱ ; ¹ ; Pramod K. Mistry^j ; ^{pramod.mistry@yale.edu}

关键词：Gaucher disease type 3 ; Enzyme replacement therapy ; Imiglucerase ; Registry ; Anemia ; Thrombocytopenia ; Hepatosplenomegaly ; Growth

刊名：Molecular Genetics and Metabolism

出版年：2017

2.Transformation in pre-treatment presentations of Gaucher disease during the first two decades of imiglucerase enzyme replacement therapy: a report from the International Collaborative Gaucher Group Gaucher Registry

作者：Neal J Weinreb^a ; Julie Batista^b ; Hans C Andersson^c ; Manisha Balwani^d ; T. Andrew Burrow^e ; Joel Charrow^f ; Paige Kaplan^g ; Aneal Khan^h ; Priya S Kishnaniⁱ ; Edwin H Kolodny^j ; Barry E Rosenbloom^k ; C. Ronald Scott^l ; Pramod K Mistry^m

刊名：Molecular Genetics and Metabolism

出版年：2017

3.Stability is maintained in adults with Gaucher disease type 1 switched from velaglucerase alfa to eliglustat or imiglucerase: A sub-analysis of the eliglustat ENCORE trial

作者：Rebecca Pleat^a ; Timothy M. Cox^b ; T. Andrew Burrow^c ; Pilar Giraldo^d ; Ozlem Goker-Alpan^e ; Barry E. Rosenbloom^f ; Laura R. Croal^a ; Lisa H. Underhill^a ; Sebastiaan J.M. Gaemers^a ; M. Judith Peterschmitt^a ; ^{Judith.Peterschmitt@genzyme.com}

关键词：Composite endpoint ; Eliglustat ; Gaucher disease type 1 ; Imiglucerase ; Non-inferiority trial ; Velaglucerase alfa

刊名：Molecular Genetics and Metabolism Reports

出版年：2016

4.Clinical response to eliglustat in treatment-naïve patients with Gaucher disease type 1: Post-hoc comparison to imiglucerase-treated patients enrolled in the International Collaborative Gaucher Group Gaucher Registry

作者：Jennifer Ibrahim ; Lisa H. Underhill ; John S. Taylor¹ ; Jennifer Angell ; M. Judith Peterschmitt ; ^{Judith.Peterschmitt@genzyme.com" class="auth_mail" title="E-mail the corresponding author}

关键词：Gaucher disease type 1 ; Eliglustat ; Substrate reduction therapy ; Acid-β-glucosidase deficiency ; Imiglucerase ; Enzyme replacement therapy

刊名：Molecular Genetics and Metabolism Reports

出版年：2016

5.Long-term velaglucerase alfa treatment in children with Gaucher disease type 1 naïve to enzyme replacement therapy or previously treated with imiglucerase

作者：Laurie Smith^a ; ^{ldsmith@cmh.edu" class="auth_mail" title="E-mail the corresponding author} ; William Rhead^b ; Joel Charrow^c ; Suma P. Shankar^d ; ^e ; Ashish Bavdekar^f ; Nicola Longo^g ; Rebecca Mardach^h ; Paul Harmatzⁱ ; Thomas Hangartner^j ; Hak-Myung Lee^k ; Eric Crombez^l ; Gregory M. Pastores^m

关键词：AE ; adverse event ; BMB ; bone marrow burden ; BW ; body weight ; CCL18 ; chemokine (C&ndash ; C motif) ligand 18 ; EOW ; every other week ; ERT ; enzyme replacement therapy ; GD ; Gaucher disease ; ICH ; International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use ; IgG ; immunoglobulin G ; IRAE ; infusion-related adverse event ; LS ; lumbar spine ; MN ; multiples of normal ; MRI ; magnetic resonance imaging ; SAE ; serious adverse event ; TEAE ; treatment-emergent ad

刊名：Molecular Genetics and Metabolism

出版年：2016

6.Risk factors for fracture in imiglucerase-treated Gaucher disease type 1 patients in the ICGG Gaucher Registry

作者：Patrick B. Deegan^a ; Julie Batista^b

刊名：Molecular Genetics and Metabolism

出版年：2016

7.Four-year follow-up from the ENCORE trial: A randomized, controlled, non-inferiority study comparing eliglustat to imiglucerase in patients with Gaucher disease type 1 stabilized on enzyme replacement therapy

作者：Timothy M. Cox^a ; Guillermo Drelichman^b ; Manisha Balwani^c ; Thomas Andrew Burrow^d ; Elena Lukina^e ; Barry Rosenbloom^f ; Sebastiaan J.M. Gaemers^g ; Jennifer Angell^g ; M. Judith Peterschmitt^g

刊名：Molecular Genetics and Metabolism

出版年：2016

8.A multicenter, open-label extension study of velaglucerase alfa in Japanese patients with Gaucher disease: Results after a cumulative treatment period of 24 months

作者：Hiroyuki Ida^a ; ^{hiroy@jikei.ac.jp" class="auth_mail" title="E-mail the corresponding author} ; Akemi Tanaka^b ; Tomoko Matsubayashi^c ; ^{matsuba@hama-med.ac.jp" class="auth_mail" title="E-mail the corresponding author} ; Kei Murayama^d ; ^{kmuraya@mri.biglobe.ne.jp" class="auth_mail" title="E-mail the corresponding author} ; Teruaki Hongo^e ; ^{hongot47@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Hak-Myung Lee^f ; ^{halee@shire.com" class="auth_mail" title="E-mail the corresponding author} ; Bjö ; rn Mellgard^g ; ^{bmellgard@shire.com" class="auth_mail" title="E-mail the corresponding author}

关键词：AE ; adverse event ; BMB ; bone marrow burden ; BMD ; bone mineral density ; BSAP ; bone-specific alkaline phosphatase ; CCL18 ; chemokine (C-C motif) ligand 18 ; CTx ; type I collagen telopeptides C-terminal cross-links ; DXA ; dual energy X-ray absorptiometry ; EOW ; every other week ; ERT ; enzyme replacement therapy ; GD ; Gaucher disease ; MRI ; magnetic resonance imaging ; NTx ; type I collagen telopeptides N-terminal cross-links ; SAE ; serious adverse event

刊名：Blood Cells, Molecules and Diseases

出版年：2016

9.Evaluation of Bone Mineral Density in Patients with Type 1 Gaucher Disease in Argentina

作者：M.S. Larroudé ; ; ¹ ; ² ; ^{mlarroude@cdrossi.com" class="auth_mail" title="E-mail the corresponding author} ; G. Aguilar¹ ; I. Rossi¹ ; G. Drelichman³ ; N. Fernandez Escobar³ ; N. Basack³ ; M. Slago⁴ ; A. Schenone⁴ ; A. Fynn⁵ ; M.F. Cuello⁵ ; R. Fernandez⁵ ; A. Ruiz⁶ ; P. Reichel⁶ ; N. Guelbert⁷ ; H. Robledo⁷ ; N. Watman⁸ ; M. Bolesina⁸ ; G. Elena⁹ ; S.E. Veber⁹ ; G. Pujal¹⁰ ; G. Galvan¹⁰ ; J.J. Chain¹¹ ; A. Arizo¹² ; J. Bietti¹² ; M. Aznar¹³ ; M. Dragosky¹⁴ ; M. Marquez¹⁴ ; L. Feldman¹⁵ ; K. Muller¹⁵ ; S. Zirone¹⁶ ; G. Buchovsky¹⁷ ; V. Lanza¹⁸ ; I. Fernandez¹⁹ ; R. Jaureguiberry²⁰ ; M.A. Barbieri²¹ ; A. Maro²¹ ; G. Zarate²² ; G. Fernandez²² ; M. Rapetti²³ ; A. Degano²⁴ ; G. Kantor²⁵ ; A. Albina²⁶ ; M. Alvarez Bollea²⁷ ; H. Arrocena²⁸ ; V. Bacciedoni²⁹ ; F. Del Rio²⁹

关键词：Argentina ; bone mineral density ; Gaucher disease ; osteoporosis

刊名：Journal of Clinical Densitometry

出版年：2016

10.Development of anti-velaglucerase alfa antibodies in clinical trial-treated patients with Gaucher disease

关键词：ADA ; anti-drug antibody ; AE ; adverse event ; CCL18 ; chemokine (C-C motif) ligand 18 ; ECL ; electrochemiluminescence ; ELISA ; enzyme-linked immunosorbent assay ; ERT ; enzyme replacement therapy ; GD ; Gaucher disease ; RIP ; radioimmunoprecipitation ; TEAE ; treatment emergent adverse event

刊名：Blood Cells, Molecules and Diseases

出版年：2016

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