1935
DOI: 10.1007/bf02163110
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Zur Pathogenese der Bronchiektasien

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Cited by 36 publications
(12 citation statements)
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“…He described four cases illustrating the triad. Later he reported seven further cases (Kartagener, 1933b;Kartagener and Horlacher, 1935) and since then the syndrome has been associated with his name. So far 82 cases have been reported in the literature, some of them having occurred in twins and siblings.…”
Section: Summaymentioning
confidence: 95%
See 1 more Smart Citation
“…He described four cases illustrating the triad. Later he reported seven further cases (Kartagener, 1933b;Kartagener and Horlacher, 1935) and since then the syndrome has been associated with his name. So far 82 cases have been reported in the literature, some of them having occurred in twins and siblings.…”
Section: Summaymentioning
confidence: 95%
“…Some people have the strange idea that you can hand a deaf aid over the counter, as you would hand out a wireless set, but the fitting of a hearing-aid is a skilled and individual process, as there is immense diversity between the needs of the patients." Although isolated cases had been reported by Siewert (1904), Oeri (1909), andGuenther (1923), Kartagener (1933a) was the first to call attention to the association of bfonchiectasis and sinus maldevelopment with transposition of the viscera. He described four cases illustrating the triad.…”
Section: Summaymentioning
confidence: 98%
“…Apart from brief case reports by Oeri (1909) and Guenther (1923), there is no further mention of the condition in the literature till Kartagener's (1933a) report of four cases, followed later by a further seven cases (Kartagener, 1933b;Kartagener and Horlacher, 1935). About the same time cases were also reported by Nuissel and Helbach (1934), Behrmann (1935), and Kautzky (1936).…”
Section: Physician West Cornwall Group Of Hospitalsmentioning
confidence: 99%
“…Bronchiectasis, chronic sinusitis, and situs inversus are the classic three abnormalities. This syndrome is a part of primary ciliary dyskinesias (PCD), a rare genetic group of diseases that involve a constitutional abnormality of the cilia leading to respiratory damages [1,2]. More rarely, PCD may be associated with cardiac, renal, or sensory defects, resulting in complex phenotypes.…”
Section: Introductionmentioning
confidence: 99%