Weiter zum Inhalt
Toggle navigation
English
English
Favoritenliste (
0
)
(Voll)
Kontakt
Mein Konto
Abmeldung
Mein Konto
Suche
Filter bei nächster Suche beibehalten
journalStr:"Orphanet Journal of Rare Diseases"
Erweiterte Suche
Suchverlauf
Struktursuche
Narrative Service
Drug Overviews
Info Guide
/vufind/Search/Results?lookfor=%22Muscular+Atrophy%22&type=Subject&filter%5B%5D=journalStr%3A%22Orphanet+Journal+of+Rare+Diseases%22
/vufind/Search/Results?lookfor=%22Muscular+Atrophy%22&type=Subject&filter%5B%5D=journalStr%3A%22Orphanet+Journal+of+Rare+Diseases%22
Search /vufind/Search2/Results?lookfor=%22Muscular+Atrophy%22&type=Subject&filter%5B%5D=journalStr%3A%22Orphanet+Journal+of+Rare+Diseases%22
PubPharm (44)
1
RegistrAME: the Spanish self-reported patient registry of spinal muscular atrophy
in:
Orphanet Journal of Rare Diseases
| 2024
von
Maria Grazia Cattinari
|
Mencía de Lemus
|
Eduardo Tizzano
Wird geladen...
2
Multidisciplinary team meetings in treatment of spinal muscular atrophy adult patients: a real-life observatory for innovative treatments
in:
Orphanet Journal of Rare Diseases
| 2024
von
Emmanuelle Salort-Campana
|
Guilhem Solé
|
Armelle Magot
| +26
Wird geladen...
3
Ultrasound-guided interlaminar approach for nusinersen administration in patients with spinal muscular atrophy with spinal fusion or severe scoliosis
in:
Orphanet Journal of Rare Diseases
| 2023
von
Cuijie Wei
|
Zhenwei Liang
|
Ying Wu
| +9
Wird geladen...
4
Prevalence of morbidities across the lifespan for adults with spinal muscular atrophy: a retrospective cohort study
in:
Orphanet Journal of Rare Diseases
| 2023
von
Daniel G. Whitney
|
Erin E. Neil Knierbein
|
Alecia K. Daunter
Wird geladen...
5
Unilateral interlaminar fenestration on the convex side provides a reliable access for intrathecal administration of nusinersen in spinal muscular atrophy: a retrospective study
in:
Orphanet Journal of Rare Diseases
| 2023
von
Zhen Wang
|
Erwei Feng
|
Yang Jiao
| +8
Wird geladen...
6
A review of the genetic spectrum of hereditary spastic paraplegias, inherited neuropathies and spinal muscular atrophies in Africans
in:
Orphanet Journal of Rare Diseases
| 2022
von
Amokelani C. Mahungu
|
Nomakhosazana Monnakgotla
|
Melissa Nel
| +1
Wird geladen...
7
Natural history of Type 1 spinal muscular atrophy: a retrospective, global, multicenter study
in:
Orphanet Journal of Rare Diseases
| 2022
von
Claude Cances
|
Dmitry Vlodavets
|
Giacomo Pietro Comi
| +12
Wird geladen...
8
Improved upper limb function in non-ambulant children with SMA type 2 and 3 during nusinersen treatment: a prospective 3-years SMArtCARE registry study
in:
Orphanet Journal of Rare Diseases
| 2022
von
Astrid Pechmann
|
Max Behrens
|
Katharina Dörnbrack
| +44
Wird geladen...
9
Short-term safety results from compassionate use of risdiplam in patients with spinal muscular atrophy in Germany
in:
Orphanet Journal of Rare Diseases
| 2022
von
Andreas Hahn
|
René Günther
|
Albert Ludolph
| +8
Wird geladen...
10
Parents as informal caregivers of children and adolescents with spinal muscular atrophy: a systematic review of quantitative and qualitative data on the psychosocial situation, caregiver burden, and family needs
in:
Orphanet Journal of Rare Diseases
| 2022
von
Maja Brandt
|
Lene Johannsen
|
Laura Inhestern
| +1
Wird geladen...
1
2
3
4
5
Nächster »
[5]
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
Ihre gewählten Filter
Filter bei nächster Suche beibehalten
Filter aufheben
Zeitschrift: Orphanet Journal of Rare Diseases
Medienart
44
Aufsätze
44
E-Artikel
44
E-Ressourcen
Zeitschriftentitel
Orphanet Journal of Rare Diseases
Thema
44
Medicine
44
R
39
Spinal muscular atrophy
8
Nusinersen
6
SMA
4
Natural history
3
Neuromuscular disease
3
Quality of life
3
Rare disease
2
Fatigability
2
Incidence
2
Lung function
2
Outcome measure
2
Prevalence
2
Qualitative research
2
Registry
2
Scoliosis
2
Spain
2
Treatment
1
1H-nuclear magnetic resonance
Alle anzeigen ...
weniger ...
Erscheinungszeitraum
35
2020-
9
2010-2019
Erscheinungsjahr(e)
Von:
Bis:
Sprache
44
Englisch
Haven't found what you're looking for?
Wird geladen...