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Ophthalmological Manifestations of Paranasal Sinus Diseases [PDF]

, 1991
Paranasal sinus diseases manifest themselves in a high percentage of eases by striking and threatening ocular and orbital signs and symptoms (Ducrey 1985; Duke-Elder 1972,1974; Ganz 1977; Herrmann 1958; Jakobiec and Jones 1986; Jakobiec et al. 1986; Seiferth and Wustrow 1977; Siegert 1975; Smith et al. 1986; Wustrow 1965).
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The Expression of Fibrinolytic Components in Chronic Paranasal Sinus Disease

American Journal of Rhinology & Allergy, 2011
Background Fibrinolytic components, their receptors, and inhibitors are considered to play an important role in inflammation and tissue remodeling including chronic rhinosinusitis (CRS). To clarify the relationship between these components and the pathology of CRS, we analyzed fibrinolytic components in sinonasal mucosa of CRS. Methods Sinonasal mucosa
Gabriele Holtappels, Takayuki Sejima, Claus Bachert   +2 more
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State of the Art Diagnostic Imaging of Paranasal Sinus Disease

Laryngo-Rhino-Otologie, 2002
The following article describes a diagnostic concept of paranasal sinus imaging, based on more than 10 years close collaboration of the authors. CT and MR are the primary imaging modalities for investigating paranasal sinus lesions. Conventional X-ray images add little information due to insufficient sensitivity.
Schuknecht B, Simmen D
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Optic Nerve Blindness due to Paranasal Sinus Disease

Ophthalmologica, 1999
Patients with total blindness caused by paranasal sinus disease have rarely been reported. We retrospectively studied the prognosis of patients who had optic nerve blindness due to paranasal sinus disease. During the past 10 years, we identified 17 patients with optic nerve disease and posterior paranasal sinus disease.
Eiko Saito, Hiroshi Nagata, Emiko Adachi-Usami, Naoya Fujimoto   +3 more
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Immunoglobulin G4–related sclerosing disease of the paranasal sinus

Head & Neck, 2012
BackgroundImmunoglobulin G4 (IgG4)–related sclerosing disease is a systemic disease characterized by extensive IgG4‐positive plasma cells and T‐lymphocyte infiltration of various organs. We present a case of a 69‐year‐old man with maxillary sinus IgG4 sclerosing disease, with orbital invasion treated with rituximab and dexamethasone pulse therapy ...
Yungpo Bernard Su, Russell B. Smith, Robert Lindau, Roger Kobayashi   +3 more
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Reliability of High-Pitch Ultra-Low-Dose Paranasal Sinus Computed Tomography for Evaluating Paranasal Sinus Anatomy and Sinus Disease

Journal of Craniofacial Surgery, 2014
The aim of this study was to evaluate the reliability of high-pitch ultra-low-dose computed tomography (CT) for detecting important paranasal sinus anatomic landmarks and pathologies.Sixty patients (22 females, 38 males) aged 15 to 67 years (mean age, 33.68 y; SD, 9.83 y) underwent high-pitch ultra-low-dose CT of the paranasal sinuses between February ...
Elif Aksoy, Hasan Tanyeri, Ercan Karaarslan, Ömer Faruk Ünal, Sila Ulus Özden   +4 more
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CT characterization of inflammatory paranasal sinus disease in cystic fibrosis

Acta Radiologica, 2002
Purpose: In patients with cystic fibrosis (CF) the prevalence of paranasal sinus affection approaches 100%. We hypothesized that the hyperviscous mucus reducing mucociliary clearance in CF patients could give sinonasal inflammatory patterns different from those in non-CF patients.
F. Kolmannskog, Signe Søvik, S. Dølvik, Heidi B. Eggesbø   +3 more
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The Surgical Diagnosis of Paranasal Sinus Disease

Radiology, 1927
The diagnosis and treatment of paranasal sinus disease encompasses a field of so extensive area, that, in this paper, I propose to generalize my remarks on the major sinuses, with a more detailed discussion of some recent observations on the ethmoid cells and sphenoidal sinus.
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Optic nerve involvement in posterior paranasal sinus diseases

Neuro-Ophthalmology, 1989
During a 13-year period, we encountered 18 cases of involvement by posterior paranasal sinus diseases in patients with optic neuritis. These could be divided into two groups, a mucocele and pyocele group (nine cases) and a sinusitis group (nine cases), both with the following clinical profile: The chief complaint was decreased vision, prodromal ...
Kahoru Shiraki, Taeko Sugimoto, Haruyuki Sotani, Shigeo Miyazaki, Masashi Shimo-Oku   +4 more
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Nasal and Paranasal Sinus Disease in Patients With Congenital Velopharyngeal Insufficiency

Archives of Otolaryngology - Head and Neck Surgery, 1994
To investigate nasal and paranasal disease in patients with congenital velopharyngeal insufficiency (CVPI).Case series.Patients with CVPI or cleft palate were investigated at Kyoto (Japan) University Hospital.Consecutive sample (60 patients with CVPI and 333 with cleft palate). No eligibility criteria or sociodemographic features. Random sample (normal
Yasuyuki Ishikawa, Ryoichi Amitani
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