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European Respiratory Journal, ISSN 0903-1936, 04/2016, Volume 47, Issue 4, pp. 1103 - 1112
Symptoms of primary ciliary dyskinesia (PCD) are nonspecific and guidance on whom to refer for testing is limited. Diagnostic tests for PCD are highly... 
TESTS | DEFECTS | MODELS | RESPIRATORY SYSTEM | DISEASE | LUNG-FUNCTION | MISSING DATA | COHORT | CHILDREN | Kartagener Syndrome - diagnosis | Prevalence | Area Under Curve | Humans | Middle Aged | Child, Preschool | Probability | Infant | Logistic Models | Male | Treatment Outcome | Young Adult | Algorithms | Sensitivity and Specificity | Adolescent | Adult | Female | ROC Curve | Aged | Child | Infant, Newborn | Index Medicus | Original
Journal Article
European Respiratory Journal, ISSN 0903-1936, 01/2017, Volume 49, Issue 1, pp. 1601090 - 1601090
Journal Article
Respirology, ISSN 1323-7799, 11/2018, Volume 23, Issue S2, pp. 51 - 52
Journal Article
European Respiratory Journal, ISSN 0903-1936, 12/2009, Volume 34, Issue 6, pp. 1264 - 1276
Journal Article
European Respiratory Journal, ISSN 0903-1936, 10/2016, Volume 48, Issue 4, pp. 1096 - 1107
Journal Article
Nature Genetics, ISSN 1061-4036, 04/2012, Volume 44, Issue 4, pp. 381 - 389
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2013, Volume 8, Issue 3, pp. e59436 - e59436
Despite recent progress in defining the ciliome, the genetic basis for many cases of primary ciliary dyskinesia (PCD) remains elusive. We evaluated five... 
SITUS-INVERSUS | CELLS | PROTEIN | GENE | MULTIDISCIPLINARY SCIENCES | LEUCINE-RICH REPEAT | OF-FUNCTION MUTATIONS | KARTAGENER-SYNDROME | PROTEOMIC ANALYSIS | BEAT FREQUENCY | IDENTIFICATION | Oligonucleotides - genetics | Chromosomes, Human, Pair 8 - genetics | RNA, Small Interfering - genetics | Humans | Molecular Sequence Data | Male | Microscopy, Video | Kartagener Syndrome - genetics | Base Sequence | HEK293 Cells | Adult | Female | Nasal Mucosa - metabolism | Gene Expression Regulation, Developmental - physiology | Genetic Linkage | Dyneins - metabolism | Amino Acid Sequence | Gene Silencing | Microscopy, Electron | Reverse Transcriptase Polymerase Chain Reaction | Genes, Recessive | Sequence Analysis, DNA | Proteins - genetics | Analysis of Variance | Pedigree | Kartagener Syndrome - pathology | Adolescent | Nasal Mucosa - cytology | Arabs - genetics | Dyneins - genetics | Proteins | Analysis | Nitric oxide | Dynein | Genetic research | Aspartate | Genetic aspects | Movement disorders | Pediatrics | Motility | Transplants & implants | Epithelial cells | Trafficking | Amino acids | Leucine | Defects | Respiratory tract | Histidine | Primary ciliary dyskinesia | Genetics | Aspartic acid | Children | Dyskinesia | Cilia | Cilia beat frequency | Zebrafish | Medicine | Acids | Insects | Chromosome 8 | Mutation | Cytoplasm | Index Medicus
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 06/2018, Volume 197, Issue 12, pp. e24 - e39
Journal Article
European Respiratory Journal, ISSN 0903-1936, 12/2010, Volume 36, Issue 6, pp. 1248 - 1258
Journal Article
The European respiratory journal, ISSN 0903-1936, 03/2018, Volume 51, Issue 3, pp. 1702221 - 1702221
Primary ciliary dyskinesia (PCD) is a chronic suppurative lung disease characterised by abnormal mucociliary clearance due to genetic defects of motile cilia.... 
CHALLENGE | ASTHMA | RECOMMENDATIONS | RESPIRATORY SYSTEM | EXERCISE | CHILDREN | Respiratory therapy | Respiratory tract | Corticoids | Primary ciliary dyskinesia | Lung diseases | Patients | Cilia | Asthma | Dyskinesia | Index Medicus
Journal Article