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topic_facet:"Muscular Dystrophy, Duchenne"
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/vufind/Search/Results?lookfor=%22muscular+dystrophy%22&type=Subject&filter%5B%5D=topic_facet%3A%22Muscular+Dystrophy%2C+Duchenne%22
/vufind/Search/Results?lookfor=%22muscular+dystrophy%22&type=Subject&filter%5B%5D=topic_facet%3A%22Muscular+Dystrophy%2C+Duchenne%22
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PubPharm (408)
1
A Study Of PGN-EDO51 In Participants With Duchenne Muscular Dystrophy Amenable To Exon 51-Skipping Treatment : A Phase 2, Open-Label, Multiple Ascending Dose Study of PGN-EDO51 With a Long-Term Extension in Participants With Duchenne Muscular Dystrophy Amenable to Exon 51-Skipping Treatment (CONNECT1-EDO51)
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| 2024
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2
A Study to Evaluate the Safety and Tolerability of GEN6050X in Duchenne Muscular Dystrophy. : A Single-arm, Open-label, Single-center Study to Evaluate the Safety and Tolerability of Intravenous GEN6050X Gene Therapy in Ambulatory Boys With Duchenne Muscular Dystrophy (DMD).
enthalten in:
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| 2024
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3
Study of AOC 1044 in Healthy Adult Volunteers and Participants With Duchenne Muscular Dystrophy (DMD) Mutations Amenable to Exon 44 Skipping : A Phase 1/2, Randomized, Placebo-controlled, Double-blind, Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamic Effects of Single and Multiple Ascending Doses of AOC 1044 Administered Intravenously to Healthy Adult Volunteers and Participants With DMD Mutations Amenable to Exon 44 Skipping
enthalten in:
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| 2024
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4
Assessments in Patients With Muscular Pathology and in Control Subjects : The ActiLiège Next Study : Gait Analysis Parameter, Stair Climbing and Upper Limb Evaluation in Patients With Muscular Pathology and in Control Subjects: The ActiLiège Next Study
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| 2024
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5
Upper Extremity Muscle Strength, Balance and Functional Skills in DMD : The Association Between Upper Extremity Muscle Strength, Balance and Functional Skills in Children With Duchenne Muscular Dystrophy
enthalten in:
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| 2024
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6
Study of Ataluren in Previously Treated Participants With Nonsense Mutation Dystrophinopathy (nmDBMD) : An Open-Label, Safety Study for Ataluren (PTC124) Patients With Nonsense Mutation Dystrophinopathy
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| 2024
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7
Halt cardiomyOPathy progrEssion in Duchenne (HOPE-OLE) : Open-Label Extension of the Halt Cardiomyopathy Progression in Duchenne (HOPE-Duchenne) Trial (CAP-1002-DMD-03)
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| 2024
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8
A Long-term Follow-up Study of Participants Who Received Delandistrogene Moxeparvovec (SRP-9001) in a Previous Clinical Study : A Phase 3, Multinational, Long-term Follow-up Study to Evaluate Safety and Efficacy in Subjects Who Have Previously Received SRP-9001 in a Clinical Study
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| 2024
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9
Rehabilitation in Muscular Dystrophies From the Hospital Facility to the Home: Pilot Project [RIMUDI] : Rehabilitation in Muscular Dystrophies From the Hospital Facility to the Home: Pilot Project
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| 2024
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10
At-Home Research Study for Patients With Autoimmune, Inflammatory, Genetic, Hematological, Infectious, Neurological, CNS, Oncological, Respiratory, Metabolic Conditions : A Multi-Site Tissue Repository Providing Annotated Biospecimens for Approved Investigator-Directed Biomedical Research Initiatives
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| 2024
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Thema: Muscular Dystrophy, Duchenne
Medienart
406
E-Ressourcen
403
Aufsätze
403
E-Artikel
5
Bücher
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Zeitschriftentitel
399
ClinicalTrials.gov
3
Arquivos de Neuro-Psiquiatria
1
Journal of Korean medical science
Thema
Muscular Dystrophy, Duchenne
399
610
396
Muscular Dystrophies
291
Study Type: Interventional
188
Recruitment Status: Completed
112
Medical Condition: Duchenne Muscular Dystrophy
100
Study Type: Observational
84
Phase: Phase 2
82
Recruitment Status: Recruiting
46
Phase: Phase 3
43
Recruitment Status: Terminated
40
Phase: Phase 1
26
Phase: Phase 1, Phase 2
26
Recruitment Status: Active, not recruiting
20
Recruitment Status: Unknown status
18
Medical Condition: Muscular Dystrophy, Duchenne
17
Phase: Phase 1/Phase 2
16
Recruitment Status: Not yet recruiting
14
Cardiomyopathies
13
Recruitment Status: Enrolling by invitation
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Erscheinungszeitraum
275
2020-
128
2010-2019
4
2000-2009
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408
Englisch
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