Results 221 to 230 of about 16,014 (252)
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Current Paediatrics, 1998
Most medical students can remember that Kartagener Syndrome is the association of situs inversus, bronchiectasis and sinusitis as a result of defective ciliary function. What is equally important but seldom remembered is that 50% of patients with primary ciliary dyskinesia (PCD) do not have situs inversus.
Maggie Meeks, Andy Bush
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Most medical students can remember that Kartagener Syndrome is the association of situs inversus, bronchiectasis and sinusitis as a result of defective ciliary function. What is equally important but seldom remembered is that 50% of patients with primary ciliary dyskinesia (PCD) do not have situs inversus.
Maggie Meeks, Andy Bush
openaire +1 more source
Understanding primary ciliary dyskinesia
Pediatric PulmonologyAbstractPrimary ciliary dyskinesia (PCD) is a rare, inherited disease characterized by impaired motile ciliary function leading to chronic sinopulmonary disease, persistent middle ear effusions, laterality defects, and subfertility. Over fifty PCD‐associated genes have also been identified, which have provided new insights into the processes involved ...
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The impact of primary ciliary dyskinesia on female and male fertility: a narrative review
Human Reproduction Update, 2023, Jane S Lucas, Ying C Cheong
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Attenuation of levodopa-induced dyskinesia by normalizing dopamine D3 receptor function
Nature Medicine, 2003Holger Stark +2 more
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Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry
Nature Genetics, 2002Richard Reinhardt +2 more
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Loss of bidirectional striatal synaptic plasticity in L-DOPA–induced dyskinesia
Nature Neuroscience, 2003Barbara Picconi +2 more
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Pathophysiology of levodopa-induced dyskinesia: Potential for new therapies
Nature Reviews Neuroscience, 2001Erwan Bezard, Jonathan M Brotchie
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