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/vufind/Search/Results?lookfor=%22Agalsidase+alfa%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
/vufind/Search/Results?lookfor=%22Agalsidase+alfa%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
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PubPharm (191)
1
Successful treatment using agalsidase alfa of a patient with Fabry disease who had anaphylaxis after agalsidase beta : A case report
enthalten in:
Northern clinics of Istanbul
| 2024
von
Cakmak, M.
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2
Updated Evaluation of Agalsidase Alfa Enzyme Replacement Therapy for Patients with Fabry Disease : Insights from Real-World Data
enthalten in:
Drug design, development and therapy
| 2024
von
Feriozzi, S.
|
Chimenti, C.
|
Reisin, R.
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3
Updated Evaluation of Agalsidase Alfa Enzyme Replacement Therapy for Patients with Fabry Disease: Insights from Real-World Data
in:
Drug Design, Development and Therapy
| 2024
von
Feriozzi S
|
Chimenti C
|
Reisin RC
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4
Safety and efficacy of pegunigalsidase alfa in patients with Fabry disease who were previously treated with agalsidase alfa : results from BRIDGE, a phase 3 open-label study
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Linhart, A.
|
Dostálová, G.
|
Nicholls, K.
| +11
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5
Effects of Agalsidase Alfa Enzyme Replacement Therapy on Left Ventricular Hypertrophy on Electrocardiogram in a Female Patient with Fabry Disease
enthalten in:
International heart journal
| 2023
von
Nakamura, K.
|
Morita, H.
|
Takaya, Y.
| +6
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6
New insights in efficacy of different ERT dosages in Fabry disease: Switch and switch-back studies data following agalsidase beta shortage. Update of systematic review
in:
Genetics in Medicine Open
| 2023
von
Eleonora Riccio
|
Carlo Garofalo
|
Ivana Capuano
| +6
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7
Twenty years of the Fabry Outcome Survey (FOS) : insights, achievements, and lessons learned from a global patient registry
enthalten in:
Orphanet journal of rare diseases
| 2022
von
Beck, M.
|
Ramaswami, U.
|
Hernberg-Ståhl, E.
| +12
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8
Twenty years of the Fabry Outcome Survey (FOS): insights, achievements, and lessons learned from a global patient registry
enthalten in:
Orphanet journal of rare diseases
| 2022
von
Beck, M.
|
Ramaswami, U.
|
Hernberg-Ståhl, E.
| +12
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9
Twenty years of the Fabry Outcome Survey (FOS): insights, achievements, and lessons learned from a global patient registry
enthalten in:
Orphanet journal of rare diseases
| 2022
von
Beck, M.
|
Ramaswami, U.
|
Hernberg-Ståhl, E.
| +12
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10
Twenty years of the Fabry Outcome Survey (FOS): insights, achievements, and lessons learned from a global patient registry
in:
Orphanet Journal of Rare Diseases
| 2022
von
Michael Beck
|
Uma Ramaswami
|
Elizabeth Hernberg-Ståhl
| +12
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Molecular genetics and metabolism
10
Journal of inherited metabolic disease
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Orphanet journal of rare diseases
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Acta paediatrica (Oslo, Norway : 1992)
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Der Nephrologe
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Thema
159
agalsidase alfa
155
Journal Article
149
EC 3.2.1.22
149
alpha-Galactosidase
145
2HLC17MX9G
145
Isoenzymes
145
Recombinant Proteins
66
Research Support, Non-U.S. Gov't
65
agalsidase beta
63
Fabry disease
57
RZD65TSM9U
36
Review
32
Agalsidase alfa
27
Enzyme replacement therapy
27
enzyme replacement therapy
25
71965-57-6
25
Trihexosylceramides
25
globotriaosylceramide
17
Multicenter Study
16
Comparative Study
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2020-
98
2010-2019
61
2000-2009
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6
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