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Italy-KV-KV Azienda Directories

Liste d'affari ed elenchi di società:
Kvesto Enzo
Indirizzo commerciale:  Salita al Monbeu 14,Trieste Ts 34100 - IT,,Italy
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KVERNELAND MALETTI SPA
Indirizzo commerciale:  Str. Ponte Alto 74,41100 MODENA (MO) - ITALY,,Italy
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Kvalito IT
Indirizzo commerciale:  Grensen 17,Oslo, Oslo - Norway,,Italy
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KVAERNER HEURTEY ITALIANA Srl
Indirizzo commerciale:  Via Marco Aurelio 8,20127 MILANO (MI) - ITALY,,Italy
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Show 1-4 record,Total 4 record










Azienda News:
  • How Does Cystic Fibrosis (CF) Cause Nasal Polyps?
    If surgery is required, patients report that it greatly improves headaches, congestion, and runny nose One study found that people with CF had fewer hospital stays in the first six months after sinus surgery 4 Some researchers believe that cystic fibrosis-related nasal polyps are different from nasal polyps caused by other health conditions 5
  • Nasal Polyps in Cystic Fibrosis - CHEST
    Nasal polyps frequently appear in patients with cystic fibrosis (CF) The aims of this study were to focus on what problems (symptoms, endoscopic findings, and laboratory correlates) nasal polyps cause the CF patient, and how these correlate to the total health situation of this patient group
  • Nasal Polyps in Cystic Fibrosis Patients: Causes, Symptoms, and . . .
    Treatment for nasal polyps in cystic fibrosis patients aims to alleviate symptoms, reduce inflammation, and prevent recurrence The approach depends on the severity of the condition and the patient’s overall health 1 Medications Intranasal Corticosteroids: These are the first-line treatment for nasal polyps They help reduce inflammation
  • Why Do Cystic Fibrosis Patients Get Nasal Polyps?
    Why Do Cystic Fibrosis Patients Get Nasal Polyps Why Do Cystic Fibrosis Patients Get Nasal Polyps Useful Articles on the Topic Article Description Site
  • Etiology of Nasal Polyps in Cystic Fibrosis: Not a Unimodal Disease
    Agents capable of reducing extracellular DNA may help manage sinusitis in CF patients Keywords: cystic fibrosis, DNA, eosinophil, histology, mucolytic, nasal Chi EY Degranulation of cystic fibrosis nasal polyp mast cells J Pathol 1992;166:395–404 doi: 10 1002 path 1711660412 [Google Scholar] ACTIONS View on publisher site;
  • Sinonasal Manifestations of Cystic Fibrosis - Medscape
    The investigators found that in patients with cystic fibrosis who had nasal polyps and the poorest baseline scores on the QOD, the drug combination led to clinically significant change In patients with better baseline QOD scores, however, the treatment tended to produce qualitative score improvements that were nonetheless not clinically
  • Chronic rhinosinusitis and nasal polyposis in cystic fibrosis: update . . .
    Although cystic fibrosis (CF) is an irreversible genetic disease, advances in treatment have increased the life expectancy of CF patients Upper airway involvement, which is mainly due to pathological changes in the paranasal sinuses, is prevalent in CF patients, although many are only mildly sympto …
  • Nasal polyps in cystic fibrosis - American Academy of Allergy, Asthma . . .
    I have a teenage patient with cystic fibrosis who has had severe recurrent nasal polyps requiring multiple surgeries Other than the nasal polyps and some GI issues, her CF has been of a generally mild phenotype Her nasal polyps have recurred despite faithfully using nasal steroids Allergy testing showed minimal allergic sensitization
  • Treatment and Prognosis of Nasal Polyps in Cystic Fibrosis
    Simple polypectomy was an adequate procedure for patients with substantial nasal symptoms There were no visual complications Other surgical complications were rare Children and adolescents with nasal polyps should have sweat tests by pilocarpine iontophoresis to rule out cystic fibrosis (Am J Dis Child 1982;136:1067-1070)
  • Nasal Polyps in Cystic Fibrosis - SpringerLink
    Nasal polyps are common in cystic fibrosis (CF) Nasal polyps in children should prompt appropriate investigations for the potential diagnosis of CF Possible etiologies for nasal polyp formation in CF include direct consequence of #916;F508 affecting chromosome 7,




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