Results 121 to 130 of about 1,525 (164)
Терапевтический архив, 2003 Some of the next articles are maybe not open access.
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New England Journal of Medicine, 2021
Kartagener’s Syndrome A 46-year-old woman presented with cough, shortness of breath, and fevers.
Kenneth Zurcher, Akira Kawashima
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Kartagener’s Syndrome A 46-year-old woman presented with cough, shortness of breath, and fevers.
Kenneth Zurcher, Akira Kawashima
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EuroIntervention, 2007
289 A 46-year-old man with Kartagener’s Syndrome (primary ciliary diskinesia, autosomal recessive disorder with dextrocardia, situs inversus, bronchiectasis and paranasal sinusitis) presented with new onset angina. Coronary arteriography revealed severe three-vessel disease with occluded left anterior descending and circumflex coronary arteries. Due to
Annick, Weustink +3 more
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289 A 46-year-old man with Kartagener’s Syndrome (primary ciliary diskinesia, autosomal recessive disorder with dextrocardia, situs inversus, bronchiectasis and paranasal sinusitis) presented with new onset angina. Coronary arteriography revealed severe three-vessel disease with occluded left anterior descending and circumflex coronary arteries. Due to
Annick, Weustink +3 more
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Chest, 1972
Clinical observations of 19 patients with Kartagener's syndrome seen during the past 25 years support the concept of congenital functional or anatomic defects in the mucociliary epithelium and its supporting structures. The case of a woman with this syndrome, who is alive at the age of 72 years, is detailed to suggest that, with reasonable medical ...
R D, Miller, M B, Divertie
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Clinical observations of 19 patients with Kartagener's syndrome seen during the past 25 years support the concept of congenital functional or anatomic defects in the mucociliary epithelium and its supporting structures. The case of a woman with this syndrome, who is alive at the age of 72 years, is detailed to suggest that, with reasonable medical ...
R D, Miller, M B, Divertie
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Dentomaxillofacial Radiology, 2006
Kartagener syndrome (KS), an autosomal recessively inherited disease, is characterized by the triad of situs inversus, bronchiectasis and sinusitis. This disorder affects the activity of proteins important to the movement of cilia, especially in the respiratory tract and the spermatozoa, developing a series of systemic alterations, which can be ...
M S, Casanova +3 more
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Kartagener syndrome (KS), an autosomal recessively inherited disease, is characterized by the triad of situs inversus, bronchiectasis and sinusitis. This disorder affects the activity of proteins important to the movement of cilia, especially in the respiratory tract and the spermatozoa, developing a series of systemic alterations, which can be ...
M S, Casanova +3 more
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Archives of Surgery, 1959
The purpose of this paper is to report a case of Kartagener's syndrome. The occurrence of situs inversus and bronchiectasis was first noted in 1904 by Siewert,4who described a case of situs inversus in a 20-year-old youth. The triad of situs inversus, bronchiectasis, and paranasal sinusitis has been more fully described by Adams and Churchill ...
B G, STREETE, F E, STULL
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The purpose of this paper is to report a case of Kartagener's syndrome. The occurrence of situs inversus and bronchiectasis was first noted in 1904 by Siewert,4who described a case of situs inversus in a 20-year-old youth. The triad of situs inversus, bronchiectasis, and paranasal sinusitis has been more fully described by Adams and Churchill ...
B G, STREETE, F E, STULL
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Kartagener's Syndrome in Childhood
Archives of Pediatrics & Adolescent Medicine, 1971Kartagener's syndrome is manifest by the association of sinusitis, situs inversus, and bronchiectasis. We treated three children with Kartagener's syndrome, two of them sisters. Respiratory symptoms began in infancy in all three patients. In case 1, a normal bronchogram was seen at 6 years of age; a second bronchogram at 13 years was grossly abnormal ...
J V, Hartline, P S, Zelkowitz
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Inheritance of Kartagener syndrome
American Journal of Medical Genetics, 1981AbstractThe surmised autosomal recessive inheritance of situs inversus of Kartagener syndrome is re‐examined on the hypothesis that the homozygous state replaces lateralization of the viscera in normal ontogeny by an indifferent lateralization. The segregation ratio in the progeny of two carrier parents (if there were no ascertainment bias) would then ...
A, Moreno, E A, Murphy
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