Found: 16
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Intracranial hemorrhage and other symptoms in infants associated with human parechovirus in Vienna, Austria.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Effect of nusinersen on motor, respiratory and bulbar function in early-onset spinal muscular atrophy.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 2, p. 668, doi. 10.1093/brain/awac252
- By:
- Publication type:
- Article
Time to diagnosis of Duchenne muscular dystrophy in Austria and Germany.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-022-27289-2
- By:
- Publication type:
- Article
Treatment effect of idebenone on inspiratory function in patients with Duchenne muscular dystrophy.
- Published in:
- Pediatric Pulmonology, 2017, v. 52, n. 4, p. 508, doi. 10.1002/ppul.23547
- By:
- Publication type:
- Article
SMArtCARE - A platform to collect real-life outcome data of patients with spinal muscular atrophy.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Functional electrical stimulation combined with botulinum toxin type A to improve hand function in children with spastic hemiparesis - a pilot study.
- Published in:
- Wiener Klinische Wochenschrift, 2011, v. 123, n. 3/4, p. 100, doi. 10.1007/s00508-010-1518-7
- By:
- Publication type:
- Article
Improved upper limb function in non-ambulant children with SMA type 2 and 3 during nusinersen treatment: a prospective 3-years SMArtCARE registry study.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Genetic spectrum of hereditary neuropathies with onset in the first year of life.
- Published in:
- Brain: A Journal of Neurology, 2011, v. 134, n. 9, p. 2664, doi. 10.1093/brain/awr184
- By:
- Publication type:
- Article
Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia.
- Published in:
- Brain: A Journal of Neurology, 2011, v. 134, n. 1, p. 143, doi. 10.1093/brain/awq287
- By:
- Publication type:
- Article
Mutations in the ganglioside‐induced differentiation‐associated protein‐1 (GDAP1) gene in intermediate type autosomal recessive Charcot–Marie–Tooth neuropathy.
- Published in:
- Brain: A Journal of Neurology, 2003, v. 126, n. 3, p. 642, doi. 10.1093/brain/awg068
- By:
- Publication type:
- Article
Improvements in Walking Distance during Nusinersen Treatment – A Prospective 3-year SMArtCARE Registry Study.
- Published in:
- Journal of Neuromuscular Diseases, 2023, v. 10, n. 1, p. 29, doi. 10.3233/JND-221600
- By:
- Publication type:
- Article
Clinical and Magnetic Resonance Imaging Outcome Predictors in Pediatric Anti-N-Methyl-D-Aspartate Receptor Encephalitis.
- Published in:
- 2020
- By:
- Publication type:
- journal article
SNP array-based whole genome homozygosity mapping as the first step to a molecular diagnosis in patients with Charcot-Marie-Tooth disease.
- Published in:
- Journal of Neurology, 2012, v. 259, n. 3, p. 515, doi. 10.1007/s00415-011-6213-8
- By:
- Publication type:
- Article
Neugeborenenscreeningprogramm für die spinale Muskelatrophie.
- Published in:
- Der Nervenarzt, 2022, v. 93, n. 2, p. 135, doi. 10.1007/s00115-021-01204-y
- By:
- Publication type:
- Article
Nichtgehfähige Patienten mit Duchenne-Muskeldystrophie: Empfehlungen zur Dokumentation des Krankheits- und Therapieverlaufs.
- Published in:
- Der Nervenarzt, 2019, v. 90, n. 8, p. 817, doi. 10.1007/s00115-019-0754-y
- By:
- Publication type:
- Article
Low mortality and short-term morbidity in very preterm infants in Austria 2011-2016.
- Published in:
- 2019
- By:
- Publication type:
- journal article