Weiter zum Inhalt
Toggle navigation
English
English
Favoritenliste (
0
)
(Voll)
Kontakt
Mein Konto
Abmeldung
Mein Konto
Suche
Erweiterte Suche
Suchverlauf
Struktursuche
Narrative Service
Drug Overviews
Info Guide
/vufind/Search/Results?lookfor=%22Kwon%2C+Jennifer+M.%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Kwon%2C+Jennifer+M.%22&type=Person&sort=year
Search /vufind/Search2/Results?lookfor=%22Kwon%2C+Jennifer+M.%22&type=Person&sort=year
PubPharm (97)
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
Wird geladen...
2
Development and assessment of educational materials for spinal muscular atrophy carrier screening in the Plain community
enthalten in:
Journal of genetic counseling
| 2024
von
Eichten, C.
|
Kuhl, A.
|
Baker, M.
| +3
Wird geladen...
3
Onasemnogene abeparvovec for presymptomatic infants with two copies of SMN2 at risk for spinal muscular atrophy type 1 : the Phase III SPR1NT trial
enthalten in:
Nature medicine
| 2022
von
Strauss, K.
|
Farrar, M.
|
Muntoni, F.
| +17
CommentIn: Nat Med. 2022 Jul;28(7):1348-1349. - PMID 35840728
Wird geladen...
4
Onasemnogene abeparvovec for presymptomatic infants with three copies of SMN2 at risk for spinal muscular atrophy : the Phase III SPR1NT trial
enthalten in:
Nature medicine
| 2022
von
Strauss, K.
|
Farrar, M.
|
Muntoni, F.
| +18
CommentIn: Nat Med. 2022 Jul;28(7):1348-1349. - PMID 35840728
Wird geladen...
5
An expanded access program of risdiplam for patients with Type 1 or 2 spinal muscular atrophy
enthalten in:
Annals of clinical and translational neurology
| 2022
von
Kwon, J.
|
Arya, K.
|
Kuntz, N.
| +12
Wird geladen...
6
Autoimmune Encephalitis : Distinguishing Features and Specific Therapies
enthalten in:
Critical care clinics
| 2022
von
Co, D.
|
Kwon, J.
Wird geladen...
7
Newborn screening for spinal muscular atrophy : The Wisconsin first year experience
enthalten in:
Neuromuscular disorders : NMD
| 2022
von
Baker, M.
|
Mochal, S.
|
Dawe, S.
| +6
Wird geladen...
8
An expanded access program of risdiplam for patients with Type 1 or 2 spinal muscular atrophy
enthalten in:
Annals of Clinical and Translational Neurology
| 2022
von
Kwon, J.
|
Arya, K.
|
Kuntz, N.
| +11
Wird geladen...
9
Expert recommendations and clinical considerations in the use of onasemnogene abeparvovec gene therapy for spinal muscular atrophy
enthalten in:
Muscle & nerve
| 2021
von
Kichula, E.
|
Proud, C.
|
Farrar, M.
| +4
Wird geladen...
10
Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy in patients with two copies of SMN2 (STR1VE) : an open-label, single-arm, multicentre, phase 3 trial
enthalten in:
The Lancet. Neurology
| 2021
von
Day, J.
|
Finkel, R.
|
Chiriboga, C.
| +18
CommentIn: Lancet Neurol. 2021 Apr;20(4):251-252. - PMID 33743228
Wird geladen...
1
2
3
4
5
6
7
8
9
10
Nächster »
[10]
Filter & Sortierung
Treffer pro Seite
10
20
50
Sortieren
Relevanz
Neueste zuerst
Älteste zuerst
Verfasser
Zeitschriftentitel
Bibliothek
Standort (Printmedien)
Verwandte Substanzen
Verwandte Substanzen werden ermittelt...
Verwandte Erkrankungen/Symptome
Verwandte Erkrankungen/Symptome werden ermittelt...
Verwandte Gene
Verwandte Gene werden ermittelt...
Systematic Reviews
Clinical Studies
Patente
Covid-19/SARS-CoV-2
Exclude Systematic Reviews
Exclude Clinical Studies
Exclude Patents
Medienart
97
Aufsätze
49
Gedruckte Aufsätze
48
E-Artikel
48
E-Ressourcen
Zeitschriftentitel
8
Journal of child neurology
7
American journal of human genetics
7
Journal of inherited metabolic disease
7
Molecular genetics and metabolism
5
Genetics in medicine
4
Pediatric neurology
3
Genetics in medicine : official journal of the ...
3
Human genetics <Berlin>
3
Muscle & nerve
2
Annals of neurology
2
Biological psychiatry
2
Contemporary clinical trials
2
Human genetics
2
Human molecular genetics
2
Molecular and cellular biology
2
Nature medicine
2
Neurologic clinics
2
Neuroscience letters
2
Orphanet journal of rare diseases
2
Pediatrics
Alle anzeigen ...
weniger ...
Thema
38
Journal Article
17
Research Support, Non-U.S. Gov't
11
Research Support, N.I.H., Extramural
9
Review
7
Newborn screening
5
Multicenter Study
5
Spinal muscular atrophy
4
Comparative Study
4
Duchene muscular dystrophy
4
Neurology
4
Neuromuscular disorders
4
Research Support, U.S. Gov't, P.H.S.
3
Bacterial Artificial Chromo
3
Batten Disease
3
Case Reports
3
Clinical Trial, Phase III
3
Duchenne muscular dystrophy
3
Genotyping Restriction Fragment Length Polymorp...
3
Intelligible Speech
3
Marker D10S583
Alle anzeigen ...
weniger ...
Erscheinungszeitraum
87
2000-
2
1900-1999
Erscheinungsjahr(e)
Von:
Bis:
Sprache
64
Englisch
Haven't found what you're looking for?
Wird geladen...