Primary ciliary dyskinesia (PCD) is a rare disease, characterised by chronic airway infection. In cystic fibrosis, FEV1 is insensitive to detect patients with structural damage, and Lung Clearance Index (LCI) was proposed as a better marker of early lung damage. In PCD, the relationship between functional and structural abnormalities has been less studied. We aimed to re-examine this in a cohort of children and adults with mild to moderate PCD.status: publishe
Background Primary ciliary dyskinesia (PCD) is generally likened to cystic fibrosis (CF) due to simi...
BACKGROUND: Structural lung changes seen on computed tomography (CT) scans in Cystic Fibrosis (CF) a...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Primary ciliary dyskinesia (PCD) is a rare disease, characterised by chronic airway infection. In cy...
Primary ciliary dyskinesia (PCD) has been considered to be relatively mild disease, especially compa...
Primary ciliary dyskinesia (PCD) has been considered a relatively mild disease, especially compared ...
Background: Primary ciliary dyskinesia (PCD) is characterized by impaired mucociliary clearance that...
Background: High-resolution CT (HRCT) scan data on primary ciliary dyskinesia (PCD) related lung dis...
Primary ciliary dyskinesia is a condition in which abnormal cilia structure or function leads to red...
Primary ciliary dyskinesia (PCD) presents with symptoms early in life and the disease course may be ...
Primary ciliary dyskinesia (PCD) presents with symptoms early in life and the disease course may be ...
Functional and structural lung evaluations are part of the follow-up of patients with primary ciliar...
Introduction and objectives Mutation type may affect clinical phenotype in PCD, as shown by differen...
BACKGROUND: Primary ciliary dyskinesia (PCD) and cystic fibrosis (CF) are increasingly compared. Th...
RATIONALE Primary ciliary dyskinesia (PCD) is an inherited disorder characterized by heterogeneous ...
Background Primary ciliary dyskinesia (PCD) is generally likened to cystic fibrosis (CF) due to simi...
BACKGROUND: Structural lung changes seen on computed tomography (CT) scans in Cystic Fibrosis (CF) a...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Primary ciliary dyskinesia (PCD) is a rare disease, characterised by chronic airway infection. In cy...
Primary ciliary dyskinesia (PCD) has been considered to be relatively mild disease, especially compa...
Primary ciliary dyskinesia (PCD) has been considered a relatively mild disease, especially compared ...
Background: Primary ciliary dyskinesia (PCD) is characterized by impaired mucociliary clearance that...
Background: High-resolution CT (HRCT) scan data on primary ciliary dyskinesia (PCD) related lung dis...
Primary ciliary dyskinesia is a condition in which abnormal cilia structure or function leads to red...
Primary ciliary dyskinesia (PCD) presents with symptoms early in life and the disease course may be ...
Primary ciliary dyskinesia (PCD) presents with symptoms early in life and the disease course may be ...
Functional and structural lung evaluations are part of the follow-up of patients with primary ciliar...
Introduction and objectives Mutation type may affect clinical phenotype in PCD, as shown by differen...
BACKGROUND: Primary ciliary dyskinesia (PCD) and cystic fibrosis (CF) are increasingly compared. Th...
RATIONALE Primary ciliary dyskinesia (PCD) is an inherited disorder characterized by heterogeneous ...
Background Primary ciliary dyskinesia (PCD) is generally likened to cystic fibrosis (CF) due to simi...
BACKGROUND: Structural lung changes seen on computed tomography (CT) scans in Cystic Fibrosis (CF) a...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...