Pages that link to "Q34142777"
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The following pages link to Primary ciliary dyskinesia: age at diagnosis and symptom history (Q34142777):
Displaying 50 items.
- Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia (Q24306694) (← links)
- Splice-site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesia (Q24306741) (← links)
- DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects (Q24318839) (← links)
- Primary ciliary dyskinesia (Siewert's/Kartagener's syndrome): respiratory symptoms and psycho-social impact (Q24805598) (← links)
- Clinical spectrum of primary ciliary dyskinesia in childhood (Q26767007) (← links)
- Diagnosis and management of primary ciliary dyskinesia (Q26999374) (← links)
- Diagnosing primary ciliary dyskinesia: an international patient perspective (Q27321360) (← links)
- PICADAR: a diagnostic predictive tool for primary ciliary dyskinesia (Q27321411) (← links)
- Inactivation of Chibby affects function of motile airway cilia (Q28585930) (← links)
- Diagnostic Support for Selected Paediatric Pulmonary Diseases Using Answer-Pattern Recognition in Questionnaires Based on Combined Data Mining Applications--A Monocentric Observational Pilot Study (Q30000042) (← links)
- Primary ciliary dyskinesia: evaluation using cilia beat frequency assessment via spectral analysis of digital microscopy images. (Q30502506) (← links)
- Quantitative analysis of ciliary beating in primary ciliary dyskinesia: a pilot study (Q30533929) (← links)
- Primary ciliary dyskinesia: critical evaluation of clinical symptoms and diagnosis in patients with normal and abnormal ultrastructure (Q30577804) (← links)
- Cilia distribution and polarity in the epithelial lining of the mouse middle ear cavity (Q30843326) (← links)
- Primary Ciliary Dyskinesia: An Update on Clinical Aspects, Genetics, Diagnosis, and Future Treatment Strategies (Q33780616) (← links)
- Mucociliary transport using 99mTc-albumin colloid: a reliable screening test for primary ciliary dyskinesia (Q34557180) (← links)
- Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome (Q34609964) (← links)
- Diseases of the nose and paranasal sinuses in child (Q34751071) (← links)
- Recent advances in primary ciliary dyskinesia genetics. (Q34852544) (← links)
- How has research in the last five years changed my clinical practice? (Q35284521) (← links)
- Update of respiratory tract disease in children with primary ciliary dyskinesia. (Q35532206) (← links)
- Variation in DNAH1 may contribute to primary ciliary dyskinesia (Q35575537) (← links)
- Primary Ciliary Dyskinesia in Children: A Review for Pediatricians, Allergists, and Pediatric Pulmonologists (Q35664961) (← links)
- Genetic Testing in the Diagnosis of Primary Ciliary Dyskinesia: State-of-the-Art and Future Perspectives (Q35667275) (← links)
- Kartagener's syndrome: review of a case series (Q35734175) (← links)
- Ciliopathies: the central role of cilia in a spectrum of pediatric disorders (Q35764547) (← links)
- Ultrastructural pathology of primary ciliary dyskinesia: report about 125 cases in Germany (Q35797827) (← links)
- Otologic features in children with primary ciliary dyskinesia. (Q35839100) (← links)
- Diagnostic accuracy of nasal nitric oxide for establishing diagnosis of primary ciliary dyskinesia: a meta-analysis (Q35860393) (← links)
- A missense mutation in TUBD1 is associated with high juvenile mortality in Braunvieh and Fleckvieh cattle (Q36029600) (← links)
- Primary ciliary dyskinesia: current state of the art. (Q36121455) (← links)
- Diagnostic needs for rare diseases and shared prediagnostic phenomena: Results of a German-wide expert Delphi survey (Q36289696) (← links)
- Kartagener's syndrome: A case series. (Q36458073) (← links)
- Primary ciliary dyskinesia and upper airway diseases (Q36616809) (← links)
- Primary ciliary dyskinesia: improving the diagnostic approach (Q36880306) (← links)
- Primary ciliary dyskinesia: recent advances in pathogenesis, diagnosis and treatment (Q36920626) (← links)
- Successful twin birth following blastocyst culture of embryos derived from the immotile ejaculated spermatozoa from a patient with primary ciliary dyskinesia: a case report (Q36970236) (← links)
- A case of Kartagener syndrome with rhinolalia clausa (Q36973278) (← links)
- Primary ciliary dyskinesia: Myths and realities (Q37021718) (← links)
- Managing wheeze in preschool children: How difficult can it be? (Q37106030) (← links)
- A review of non-cystic fibrosis pediatric bronchiectasis (Q37106325) (← links)
- Primary ciliary dyskinesia, an orphan disease (Q38025037) (← links)
- Allergic bronchopulmonary aspergillosis in an adult with Kartagener syndrome (Q38562058) (← links)
- The patient's experience of primary ciliary dyskinesia: a systematic review (Q38737398) (← links)
- A new tool improves diagnostic test performance for transmission em evaluation of axonemal dynein arms (Q38813267) (← links)
- Clinical Features and Associated Likelihood of Primary Ciliary Dyskinesia in Children and Adolescents (Q39857217) (← links)
- Successful treatment of persistent hypoxemia by nasal suctioning in a neonate with primary ciliary dyskinesia (Q42554116) (← links)
- Diagnosing primary ciliary dyskinesia (Q42764830) (← links)
- Nasal nitric oxide to diagnose primary ciliary dyskinesia in newborns (Q43141892) (← links)
- Primary ciliary dyskinesia (Pcd) in Austria (Q43240010) (← links)