Found: 8
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Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
- Published in:
- Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-015-0254-5
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- Publication type:
- Article
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
- Published in:
- 2015
- By:
- Publication type:
- journal article
CAD mutations and uridine-responsive epileptic encephalopathy.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Die deutsche Version des Neurophysiology of Pain Questionnaire: Übersetzung, transkulturelle Adaptation, Reliabilität und Validität.
- Published in:
- Der Schmerz, 2019, v. 33, n. 3, p. 244, doi. 10.1007/s00482-019-0366-2
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- Publication type:
- Article
Effect of Additional Pain Neuroscience Education in Interdisciplinary Multimodal Pain Therapy on Current Pain. A Non-Randomized, Controlled Intervention Study.
- Published in:
- Journal of Pain Research, 2020, v. 13, p. 2947, doi. 10.2147/JPR.S272943
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- Publication type:
- Article
Outcome of severe unilateral cerebellar hypoplasia.
- Published in:
- Developmental Medicine & Child Neurology, 2010, v. 52, n. 8, p. 718, doi. 10.1111/j.1469-8749.2009.03522.x
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- Publication type:
- 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
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- Publication type:
- Article
Die Anwendung von Ability Skill and Task Training (ASTT®) bei Kindern mit unilateral-spastischer Cerebralparese zur Förderung des Erwerbs alltagsorientierter bimanueller Aktivitäten -- eine Therapiemethode in der pädiatrischen Ergotherapie
- Published in:
- Ergoscience, 2017, v. 12, n. 2, p. 56, doi. 10.2443/skv-s-2017-54020170202
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- Publication type:
- Article