Results 41 to 50 of about 2,635 (172)

Topical and systemic antifungal therapy for chronic rhinosinusitis [PDF]

, 2018
Background: This review adds to a series of reviews looking at primary medical management options for patients with chronic rhinosinusitis.  Chronic rhinosinusitis is common and characterised by inflammation of the lining of the nose and paranasal ...
Balk, Bent, Braun, Chakrabarti, Chan, Chen, Cho, Chong, Chong, Chong, Corradini, Deka, DeMarcantonio, Drunen, Ebbens, Ebbens, Ebbens, Ebbens, Ebbens, Ebbens, Egger, Erskine, Fokkens, Fokkens, Frigas, Gerlinger, Gerlinger, Gliklich, Gupta, Hashemi, Hastan, Head, Head, Head, Helbling, Hofman, Hopkins, Jiang, Jiang, Joshi, Juniper, Kennedy, Kern, Keswani, Khalil, Lackner, Larsen, Liang, Lopatin, Mistry, Nikakhlagh, Panda, Patro, Philpott, Ponikau, Ponikau, Ragab, Ragab, Ravikumar, Ricchetti, Ricchetti, Rojita, Sacks, Sherris, Shin, Sok, Somu, Tan, Thamboo, Tomassen, Verma, Weschta, Weschta, Wild, Yousefi, Zhang, Zhang, Zhang   +77 more
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Ultrastructural Sperm Flagellum Defects in a Patient With CCDC39 Compound Heterozygous Mutations and Primary Ciliary Dyskinesia/Situs Viscerum Inversus

Frontiers in Genetics, 2020
Introduction: Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disease characterized by structural or functional motile cilia abnormalities. Up to 40 different genes seem, at the moment, to be involved in the pathogenesis of PCD.
Rossella Cannarella, Eugenia Tiziana Maniscalchi, Rosita Angela Condorelli, Marina Scalia, Giulia Guerri, Sandro La Vignera, Matteo Bertelli, Aldo Eugenio Calogero   +7 more
doaj   +1 more source

Kartagener Syndrome With Focal Segmental Glomerulosclerosis [PDF]

, 2013
Primary ciliary dyskinesia is characterized by congenital impairment of mucociliary clearance. Kartagener syndrome (KS) is a clinical variant of primary ciliary dyskinesia which is involved in situs inversus associated with chronic respiratory infections.
Doroushi, Behzad, Momeni, Ali, Taheri, Nadia   +2 more
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Kartagener Syndrome: A Rare Genetic Disorder

Journal of Nepal Medical Association, 2009
Kartagener Syndrome is a rare autosomal recessive disorder consisting of triad of sinusitis, bronchiectasis and situs inversus with dextrocardia. It is the subset of disorder called primary ciliary dyskinesia in which the cilia have abnormal structure ...
Kunjan Shakya
doaj   +1 more source

Large-scale analysis of disease pathways in the human interactome

, 2017
Discovering disease pathways, which can be defined as sets of proteins associated with a given disease, is an important problem that has the potential to provide clinically actionable insights for disease diagnosis, prognosis, and treatment ...
Agrawal, Monica, Leskovec, Jure, Zitnik, Marinka   +2 more
core   +1 more source

Cardiopulmonary assessment in primary ciliary dyskinesia. [PDF]

, 2012
Background Primary ciliary dyskinesia (PCD) is a rare, usually autosomal recessive disorder of ciliary dysfunction associated with lung involvement, which has a great impact on health.
GIALLAURIA, FRANCESCO, Mirra V, Montella S, SANTAMARIA, FRANCESCA, Vaino N, Valerio G, VIGORITO, CARLO   +6 more
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Kartagener Syndrome with Pan Atopic Airway Disease

APIK Journal of Internal Medicine, 2022
Kartagener syndrome (KS) is a rare type of primary ciliary dyskinesia, which comprises a triad of chronic sinusitis, situs inversus, and bronchiectasis.
Aakanksha, Saby Anna Kunjumon, Ketaki Vasudeo Utpat, Unnati Desai, Ramesh Bharmal   +4 more
doaj   +1 more source

Kartagener′s syndrome

Medical Journal of Dr. D.Y. Patil University, 2012
Bronchiectasis may have varied etiologies. In patients presenting in middle or old age with bronchiectasis, congenital and hereditary causes of bronchiectasis are not commonly encountered. In majority of adult patients, bronchiectasis follows necrotizing
Pradip V Potdar, Mitali M Nayak, Aushutosh Chitnis   +2 more
doaj   +1 more source

Genetic basis of dental agenesis - molecular genetics patterning clinical dentistry [PDF]

, 2013
Tooth agenesis is one of the most common congenital malformations in humans. Hypodontia can either occur as an isolated condition (non-syndromic hypodontia) or can be associated with a syndrome (syndromic hypodontia), highlighting the heterogeneity of ...
Chhabra, Anuj, Chhabra, Nidhi, Goswami, Mridula   +2 more
core   +1 more source

KARTAGENER SYNDROME

Gomal Journal of Medical Sciences, 2014
Kartagener Syndrome is an autosomal recessive disorder, a subgroup of primary ciliary dyskinesia, characterized by a triad of bronchiectasis, sinusitis and situs inversus.
Khalid Shakeel Babar, Habibullah Khan, Yasser Ismail, Muhammad Fawad, Qaisar Azim   +4 more
doaj