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A Comprehensive Approach for the Diagnosis of Primary Ciliary Dyskinesia—Experiences from the First 100 Patients of the PCD-UNIBE Diagnostic Center
Primary ciliary dyskinesia (PCD) is a rare genetic disease characterized by dyskinetic cilia. Respiratory symptoms usually start at birth. The lack of diagnostic gold standard tests is challenging, as PCD diagnostics requires different methods with high expertise. We founded PCD-UNIBE as the first c...
Autores principales: | Müller, Loretta, Savas, Sibel T., Tschanz, Stefan A., Stokes, Andrea, Escher, Anaïs, Nussbaumer, Mirjam, Bullo, Marina, Kuehni, Claudia E., Blanchon, Sylvain, Jung, Andreas, Regamey, Nicolas, Haenni, Beat, Schneiter, Martin, Ingold, Jonas, Kieninger, Elisabeth, Casaulta, Carmen, Latzin, Philipp |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466881/ https://www.ncbi.nlm.nih.gov/pubmed/34573882 http://dx.doi.org/10.3390/diagnostics11091540 |
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