Berdon W.E., McManus C., Afzelius B. More on Kartagener’s syndrome and the contributions of Afzelius and A.K. Siewert. „Pediatr Radiol”. 34 (7), s. 585–586, 2004. DOI: 10.1007/s00247-004-1203-y. PMID: 15164138.
Berdon W.E., Willi U. Situs inversus, bronchiectasis, and sinusitis and its relation to immotile cilia: history of the diseases and their discoverers-Manes Kartagener and Bjorn Afzelius. „Pediatr Radiol”. 34 (1), s. 38–42, 2004. DOI: 10.1007/s00247-003-1072-9. PMID: 14551758.
Moore A., Escudier E., Roger G., Tamalet A., Pelosse B., Marlin S., Clément A., Geremek M., Delaisi B., Bridoux A.M., Coste A., Witt M., Duriez B., Amselem S. RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa. „J Med Genet”. 43 (4), s. 326–333, 2006. DOI: 10.1136/jmg.2005.034868. PMID: 16055928.
De Boeck K., Proesmans M., Mortelmans L., Van Billoen B., Willems T., Jorissen M. Mucociliary transport using 99mTc-albumin colloid: a reliable screening test for primary ciliary dyskinesia. „Thorax”. 60 (5), s. 414–417, 2005. DOI: 10.1136/thx.2004.027680. PMID: 15860718.
Fliegauf M., Olbrich H., Horvath J., Wildhaber J.H., Zariwala M.A., Kennedy M., Knowles M.R., Omran H. Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia. „Am J Respir Crit Care Med”. 171 (12), s. 1343–1349, 2005. DOI: 10.1164/rccm.200411-1583OC. PMID: 15750039.
Pifferi M., Caramella D., Cangiotti A.M., Ragazzo V., Macchia P., Boner A.L. Nasal nitric oxide in atypical primary ciliary dyskinesia. „Chest”. 131 (3), s. 870–873, 2007. DOI: 10.1378/chest.06-2472. PMID: 17356106.
Berdon W.E., McManus C., Afzelius B. More on Kartagener’s syndrome and the contributions of Afzelius and A.K. Siewert. „Pediatr Radiol”. 34 (7), s. 585–586, 2004. DOI: 10.1007/s00247-004-1203-y. PMID: 15164138.
Afzelius B. A human syndrome caused by immotile cilia. „Science”. 193, s. 317–319, 1976. PMID: 1084576.
Berdon W.E., Willi U. Situs inversus, bronchiectasis, and sinusitis and its relation to immotile cilia: history of the diseases and their discoverers-Manes Kartagener and Bjorn Afzelius. „Pediatr Radiol”. 34 (1), s. 38–42, 2004. DOI: 10.1007/s00247-003-1072-9. PMID: 14551758.
Katsuhara K., Kawamoto S., Wakabayashi T., Belsky J.L. Situs inversus totalis and Kartagener’s syndrome in a Japanese population. „Chest”. 61 (1), s. 56–61, 1972. PMID: 4538074.
Torgersen J. Situs inversus, asymmetry, and twinning. „Am J Hum Genet”. 2 (4), s. 361–370, 1951. PMID: 14837905.
Bush A., Cole P., Hariri M., Mackay I., Phillips G., O’Callaghan C., Wilson R., Warner J.O. Primary ciliary dyskinesia: diagnosis and standards of care. „Eur Respir J”. 12 (4), s. 982–988, 1999. PMID: 9817179.
Waite D.A., Wakefield S.J., Moriarty K.M., Lewis M.E., Cuttance P.C., Scott A.G. Polynesian bronchiectasis. „Eur J Respir Dis Suppl”. 127, s. 31–36, 1983. PMID: 6578056.
Wakefield S., Waite D. Abnormal cilia in Polynesians with bronchiectasis. „Am Rev Respir Dis”. 121 (6), s. 1003–1010, czerwiec 1980. PMID: 6968169.
Tek I., Dinçer I., Gürlek A. Kartagener’s syndrome with dextrocardia and corrected transposition of great arteries. „Int J Cardiol”. 75 (2-3), s. 305–308, 2000. PMID: 11186968.
Pomerleau D., Gilbert G., Thibert D. [Kartagener’s syndrome associated with tetralogy of Fallot]. „Union Med Can”. 101 (1), s. 79–84, 1972. PMID: 4536858.
Moore A., Escudier E., Roger G., Tamalet A., Pelosse B., Marlin S., Clément A., Geremek M., Delaisi B., Bridoux A.M., Coste A., Witt M., Duriez B., Amselem S. RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa. „J Med Genet”. 43 (4), s. 326–333, 2006. DOI: 10.1136/jmg.2005.034868. PMID: 16055928.
Krawczyński M.R., Dmeńska H., Witt M. Apparent X-linked primary ciliary dyskinesia associated with retinitis pigmentosa and a hearing loss. „J Appl Genet”. 45 (1), s. 107–110, 2004. PMID: 14960774.
Roomans G.M., Ivanovs A., Shebani E.B., Johannesson M. Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia. „Ups J Med Sci”. 111 (1), s. 155–168, 2006. PMID: 16553254.
Coren M.E., Meeks M., Morrison I., Buchdahl R.M., Bush A. Primary ciliary dyskinesia: age at diagnosis and symptom history. „Acta Paediatr”. 91 (6), s. 667–669, 2002. PMID: 12162599.
De Boeck K., Proesmans M., Mortelmans L., Van Billoen B., Willems T., Jorissen M. Mucociliary transport using 99mTc-albumin colloid: a reliable screening test for primary ciliary dyskinesia. „Thorax”. 60 (5), s. 414–417, 2005. DOI: 10.1136/thx.2004.027680. PMID: 15860718.
Chilvers M.A., Rutman A., O’Callaghan C. Ciliary beat pattern is associated with specific ultrastructural defects in primary ciliary dyskinesia. „J Allergy Clin Immunol”. 112 (3), s. 518–524, 2003. PMID: 13679810.
Toskala E., Haataja J., Shirasaki H., Rautiainen M. Culture of cells harvested with nasal brushing: a method for evaluating ciliary function. „Rhinology”. 43 (2), s. 121–124, 2005. PMID: 16008067.
Fliegauf M., Olbrich H., Horvath J., Wildhaber J.H., Zariwala M.A., Kennedy M., Knowles M.R., Omran H. Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia. „Am J Respir Crit Care Med”. 171 (12), s. 1343–1349, 2005. DOI: 10.1164/rccm.200411-1583OC. PMID: 15750039.
Pifferi M., Caramella D., Cangiotti A.M., Ragazzo V., Macchia P., Boner A.L. Nasal nitric oxide in atypical primary ciliary dyskinesia. „Chest”. 131 (3), s. 870–873, 2007. DOI: 10.1378/chest.06-2472. PMID: 17356106.
Cayan S., Conaghan J., Schriock E.D., Ryan I.P., Black L.D., Turek P.J. Birth after intracytoplasmic sperm injection with use of testicular sperm from men with Kartagener/immotile cilia syndrome. „Fertil Steril”. 76 (3), s. 612–614, 2001. PMID: 11532490.