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PubPharm (98)
1
Long-Term Follow-Up Cares and Check Initiative : A Program to Advance Long-Term Follow-Up in Newborns Identified with a Disease through Newborn Screening
enthalten in:
International journal of neonatal screening
| 2024
von
Lietsch, M.
|
Chan, K.
|
Taylor, J.
| +11
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2
Comparative effectiveness of azathioprine and mycophenolate mofetil for myasthenia gravis (PROMISE-MG) : a prospective cohort study
enthalten in:
The Lancet. Neurology
| 2024
von
Narayanaswami, P.
|
Sanders, D.
|
Thomas, L.
| +51
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3
Prophylactic use of cardiac medications for delay of left ventricular dysfunction in Duchenne muscular dystrophy
enthalten in:
Birth defects research
| 2024
von
Conway, K.
|
Thomas, S.
|
Ciafaloni, E.
| +5
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4
Safety and efficacy of arimoclomol for inclusion body myositis : a multicentre, randomised, double-blind, placebo-controlled trial
enthalten in:
The Lancet. Neurology
| 2023
von
Machado, P.
|
McDermott, M.
|
Blaettler, T.
| +91
CommentIn: Lancet Neurol. 2023 Oct;22(10):873-874. - PMID 37739563
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5
Newborn screening for Duchenne muscular dystrophy : A two-year pilot study
enthalten in:
Annals of clinical and translational neurology
| 2023
von
Tavakoli, N.
|
Gruber, D.
|
Armstrong, N.
| +24
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6
Detecting early signs in Duchenne muscular dystrophy : comprehensive review and diagnostic implications
enthalten in:
Frontiers in pediatrics
| 2023
von
Mercuri, E.
|
Pane, M.
|
Cicala, G.
| +2
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7
Racial and Ethnic Differences in Timing of Diagnosis and Clinical Services Received in Duchenne Muscular Dystrophy
enthalten in:
Neuroepidemiology
| 2023
von
Mann, J.
|
Zhang, Y.
|
McDermott, S.
| +9
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8
Newborn Screening for Spinal Muscular Atrophy in New York State : Clinical Outcomes From the First 3 Years
enthalten in:
Neurology
| 2022
von
Lee, B.
|
Deng, S.
|
Chiriboga, C.
| +16
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9
Time to diagnosis of Duchenne muscular dystrophy remains unchanged : Findings from the Muscular Dystrophy Surveillance, Tracking, and Research Network, 2000-2015
enthalten in:
Muscle & nerve
| 2022
von
Thomas, S.
|
Conway, K.
|
Fapo, O.
| +9
CommentIn: Muscle Nerve. 2022 Aug;66(2):116-117. - PMID 35560237
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10
Selected clinical and demographic factors and all-cause mortality among individuals with Duchenne muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking, and Research Network
enthalten in:
Neuromuscular disorders : NMD
| 2022
von
Paramsothy, P.
|
Wang, Y.
|
Cai, B.
| +8
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Thema: Journal Article
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98
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Muscle & nerve
11
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9
Journal of child neurology
5
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3
Neuromuscular disorders : NMD
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The Lancet. Neurology
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American journal of medical genetics. Part A
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Thema
Journal Article
27
Research Support, U.S. Gov't, P.H.S.
26
Research Support, Non-U.S. Gov't
20
Research Support, N.I.H., Extramural
18
Duchenne muscular dystrophy
15
Review
13
Multicenter Study
11
Randomized Controlled Trial
9
Prednisone
9
VB0R961HZT
7
Immunosuppressive Agents
6
Adrenal Cortex Hormones
6
Case Reports
6
Comparative Study
6
Glucocorticoids
5
Dystrophin
5
Pregnenediones
4
5Z9SP3X666
4
Duchenne
4
KR5YZ6AE4B
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Erscheinungszeitraum
34
2020-
44
2010-2019
18
2000-2009
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98
Englisch
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