Results 101 to 110 of about 2,654 (190)

Síndrome de Kartagener, reporte de caso

Revista Médica Hondureña
Introduction: Kartagener Syndrome is a clinical variant of primary ciliary dyskinesia It is a rare autosomal recessive disease, one in every 32,000 births, characterized by a triad of bronchiectasis, chronic sinusitis and situs ...
Suyapa Sosa Ferrari, Luisa Rodríguez, Gerardo Mejía, Javier Sánchez   +3 more
doaj   +1 more source

Kartagener syndrome [PDF]

QJM: An International Journal of Medicine, 2018
D, Yang, B C, Liu, J, Luo, T X, Huang, C T, Liu   +4 more
openaire   +3 more sources

47 Year Old Patient with Pseudo-Asthma

Oman Medical Journal, 2011
47- year- old female patient presented in out-patient department in Afyon Chest Disease Hospital with dyspnea, cough and purulent sputum. She has been receiving regular inhaler β-agonist and corticosteroids with the diagnosis of asthma bronchial since ...
Bulent Altinsoy
doaj  

Loci for primary ciliary dyskinesia map to chromosome 16p12.1-12.2 and 15q13.1-15.1 in Faroe Islands and Israeli Druze genetic isolates [PDF]

, 2004
Amirav, I, Bisgaard, H, Chodhari, R, Chung, EMK, Faeroe, O, Gardiner, RM, Jeganathan, D, Luder, AS, Meeks, M, Mitchison, HM, Nielsen, K, Smyth, D   +11 more
core   +2 more sources

Novel homozygous mutations of DNAH5 in Kartagener syndrome. [PDF]

QJM, 2022
Cheng XD, Ni F, Lu Y.
europepmc   +1 more source

Kartagener syndrome [PDF]

Internal and Emergency Medicine, 2015
Suat-Jin, Lu, Suat W, Loo
openaire   +2 more sources

A founder CEP120 mutation in Jeune asphyxiating thoracic dystrophy expands the role of centriolar proteins in skeletal ciliopathies [PDF]

, 2017
Jeune asphyxiating thoracic dystrophy (JATD) is a skeletal dysplasia characterized by a small thoracic cage and a range of skeletal and extra-skeletal anomalies.
Alamro, Rana, Alkuraya, Fowzan S., Almoisheer, Agaadir, Alshiddi, Tarfa, Alzahrani, Fatma, Beales, Philip L., Faqeih, Eissa, Hashem, Amal, Holder, Isabel, Lausch, Ekkehart, Mitchison, Hannah M., Schmidts, Miriam, Shaheen, Ranad, Superti-Furga, Andrea   +13 more
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A Rare Case of Kartagener Syndrome Presenting with Sinusitis, Situs Inversus, and Bronchiectasis: Emphasizing Early Diagnosis and Management Strategies. [PDF]

Cureus, 2023
Butt SRR, Shakoor H, Khan TJ, Almaalouli B, Ekhator C, Ansari S, Shaikh N, Shehryar A, Rehman A.   +8 more
europepmc   +1 more source

Lung Transplantation for Primary Ciliary Dyskinesia and Kartagener Syndrome: A Multicenter Study. [PDF]

Transpl Int, 2023
Marro M, Leiva-Juárez MM, D'Ovidio F, Chan J, Van Raemdonck D, Ceulemans LJ, Moreno P, Kindelan AA, Krueger T, Koutsokera A, Ehrsam JP, Inci I, Yazicioglu A, Yekeler E, Boffini M, Brioude G, Thomas PA, Pizanis N, Aigner C, Schiavon M, Rea F, Anile M, Venuta F, Keshavjee S.   +23 more
europepmc   +1 more source

Update on management of rhinitis [PDF]

, 1998
Rhinitis is common in Hong Kong. The aim of treatment is to control the symptoms and to allow an undisturbed lifestyle without the side-effects of therapy. A secondary goal is to prevent the complication of sinusitis and its sequelae. Most of these goals
Ho, WK, Lam, PKY, Wei, WI
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