Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Matthias, Bischof"'
Publikováno v:
Neurology and Therapy, Vol 12, Iss 4, Pp 1205-1220 (2023)
Abstract Introduction We sought to evaluate the cost-effectiveness of newborn screening (NBS) versus no NBS for 5q spinal muscular atrophy (SMA) in England. Methods A cost-utility analysis using a combination of decision tree and Markov model structu
Externí odkaz:
https://doaj.org/article/8ba8bf0ac4f94632a823eb63a735fc06
Autor:
Rebecca Dean, Ivar Jensen, Phil Cyr, Beckley Miller, Benit Maru, Douglas M. Sproule, Douglas E. Feltner, Thomas Wiesner, Daniel C. Malone, Matthias Bischof, Walter Toro, Omar Dabbous
Publikováno v:
Journal of Market Access & Health Policy, Vol 9, Iss 1 (2021)
Background: Recent cost-utility analysis (CUA) models for onasemnogene abeparvovec (Zolgensma®, formerly AVXS-101) in spinal muscular atrophy type 1 (SMA1) differ on key assumptions and results. Objective: To compare the manufacturer’s proprietary
Externí odkaz:
https://doaj.org/article/4ff5f47c0a944bf891888597b331385c
Autor:
Rimma Velikanova, Simon van der Schans, Matthias Bischof, Rudolf Walther van Olden, Maarten Postma, Cornelis Boersma
Publikováno v:
Value in Health, 25(10), 1696-1704. ELSEVIER SCIENCE INC
Objectives: Spinal muscular atrophy (SMA) is a rare genetic disorder that causes progressive muscle weakness and paralysis. In its most common and severe form, the majority of untreated infants die before 2 years of age. Early detection and treatment
Autor:
Marjolaine Gauthier-Loiselle, Matthias Bischof, Anish Patel, O. Dabbous, Sherry Shi, Martin Cloutier, Mikhail Davidson, Nicole LaMarca, Walter Toro
Publikováno v:
Advances in Therapy
Introduction Spinal muscular atrophy (SMA) is a rare, genetic neuromuscular disorder caused by deletion/mutation of the survival motor neuron 1 gene, characterized by progressive loss of motor neurons, resulting in increasing muscular weakness, deter
Publikováno v:
Value in Health. 25:1922-1923
Autor:
Maria Lorenzi, Matthias Bischof, Eric Druyts, Jennifer M Lee, Chakrapani Balijepalli, O. Dabbous
Publikováno v:
Current medical research and opinion. 37(10)
Objective Onasemnogene abeparvovec, a one-time intravenous gene replacement therapy, and nusinersen, an antisense oligonucleotide that requires ongoing intrathecal administration, have been evaluated as treatments for spinal muscular atrophy (SMA) ty
Autor:
Phil Cyr, Matthias Bischof, Daniel C. Malone, Ivar Jensen, Benit Maru, Thomas Wiesner, Rebecca Dean, Walter Toro, Beckley Miller, Douglas E. Feltner, O. Dabbous, Douglas M. Sproule
Publikováno v:
Journal of Market Access & Health Policy, Vol 9, Iss 1 (2021)
Journal of Market Access & Health Policy
article-version (VoR) Version of Record
Journal of Market Access & Health Policy
article-version (VoR) Version of Record
Background: Recent cost-utility analysis (CUA) models for onasemnogene abeparvovec (Zolgensma®, formerly AVXS-101) in spinal muscular atrophy type 1 (SMA1) differ on key assumptions and results. Objective: To compare the manufacturer’s proprietary
Autor:
Paul Hodgkins, Juliana Setyawan, Matthias Bischof, Josephine Mauskopf, Evelina Zimovetz, Stephen Beard
Publikováno v:
CNS Drugs
Background An economic analysis from the perspective of the UK National Health Service (NHS) evaluated the cost effectiveness of lisdexamfetamine dimesylate (LDX) compared with atomoxetine in children and adolescents with attention-deficit/hyperactiv
Autor:
Eric Meggers, Manfred Jung, Klaus Harms, Matthias Bischof, Melanie Helms, Florian Ritterbusch, Peter Göbel
Publikováno v:
European Journal of Inorganic Chemistry. 2015:1654-1659
Chiral bis-cyclometalated octahedral organoiridium(III) complexes were designed to target different classes of enzymes, namely carbonic anhydrases, histone deacetylases, and serine proteases. The stereoselective non-racemic synthesis of selected comp
Autor:
Marco A. Alcala, Hyounsoo Uh, Yong J. Lee, Ruth A. Modzelewski, Shu Ying Kwan, Kristy A. Gogick, David L. Bartlett, Stéphane Petoud, Adam R. Meier, Matthias Bischof, Chad M. Shade, Timothy G. Strein, Charles K. Brown, Zachary P. Thompson
Publikováno v:
Biomaterials
Biomaterials, Elsevier, 2011, 32 (35), pp.9343-52. ⟨10.1016/j.biomaterials.2011.07.076⟩
Biomaterials, Elsevier, 2011, 32 (35), pp.9343-52. ⟨10.1016/j.biomaterials.2011.07.076⟩
International audience; We have created a dendrimer complex suitable for preferential accumulation within liver tumors and luminescence imaging by substituting thirty-two naphthalimide fluorophores on the surface of the dendrimer and incorporating ei