Characteristics of pathogenic fungi and antifungal therapy in cystic fibrosis (Q34130445)

31 July 2017

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title

Characteristics of pathogenic fungi and antifungal therapy in cystic fibrosis (English)

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31 July 2017

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Frank-Michael C Müller

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1

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Marc Seidler

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2

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publication date

1 August 2010

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Expert Review of Anti-infective Therapy

31 July 2017

published in

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31 July 2017

volume

8

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31 July 2017

issue

8

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31 July 2017

page(s)

957-964

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Chronic colonization with Pandoraea apista in cystic fibrosis patients determined by repetitive-element-sequence PCR.

31 July 2017

cites work

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Microbiology of sputum from patients at cystic fibrosis centers in the United States

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Diagnosing allergic bronchopulmonary aspergillosis in children with cystic fibrosis

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The effect of chronic infection with Aspergillus fumigatus on lung function and hospitalization in patients with cystic fibrosis

21 January 2018

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Impact of mold infections in explanted lungs on outcomes of lung transplantation

21 January 2018

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Clinical significance of Scedosporium apiospermum in patients with cystic fibrosis

21 January 2018

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Scedosporium apiospermum: changing clinical spectrum of a therapy-refractory opportunist*

21 January 2018

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21 January 2018

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Molecular epidemiology of Scedosporium apiospermum infection determined by PCR amplification of ribosomal intergenic spacer sequences in patients with chronic lung disease

21 January 2018

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Genotyping study of Scedosporium apiospermum isolates from patients with cystic fibrosis

21 January 2018

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Detection of occult Scedosporium species in respiratory tract specimens from patients with cystic fibrosis by use of selective media.

21 January 2018

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Disseminated infection by Scedosporium prolificans: an emerging fatality among haematology patients. Case report and review

21 January 2018

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Molecular typing of Australian Scedosporium isolates showing genetic variability and numerous S. aurantiacum

21 January 2018

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Bilateral endogenous Scedosporium prolificans endophthalmitis after lung transplantation.

21 January 2018

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Isolation of fungi, especially Exophiala dermatitidis, in patients suffering from cystic fibrosis. A prospective study

21 January 2018

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Exophiala dermatitidis pneumonia in cystic fibrosis

21 January 2018

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High prevalence of the neurotrope Exophiala dermatitidis and related oligotrophic black yeasts in sauna facilities

21 January 2018

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Development of a novel PCR assay for the identification of the black yeast, Exophiala (Wangiella) dermatitidis from adult patients with cystic fibrosis (CF).

21 January 2018

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21 January 2018

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Susceptibility to five antifungals of Aspergillus fumigatus strains isolated from chronically colonised cystic fibrosis patients receiving azole therapy

21 January 2018

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Emergence of azole resistance in Aspergillus fumigatus and spread of a single resistance mechanism

21 January 2018

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Epidemiological cutoffs and cross-resistance to azole drugs in Aspergillus fumigatus.

21 January 2018

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Frequency and evolution of Azole resistance in Aspergillus fumigatus associated with treatment failure

21 January 2018

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Pharmacokinetics and safety of itraconazole in patients with cystic fibrosis

21 January 2018

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A d-optimal designed population pharmacokinetic study of oral itraconazole in adult cystic fibrosis patients

21 January 2018

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Voriconazole: a new triazole antifungal agent

21 January 2018

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Voriconazole therapy in children with cystic fibrosis

21 January 2018

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Voriconazole pharmacokinetic variability in cystic fibrosis lung transplant patients

21 January 2018

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Safe management of tacrolimus together with posaconazole in lung transplant patients with cystic fibrosis

21 January 2018

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Development of an oligonucleotide array for direct detection of fungi in sputum samples from patients with cystic fibrosis

21 January 2018

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Prevalence and risk factors for recovery of filamentous fungi in individuals with cystic fibrosis.

21 January 2018

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Fungal infections in patients with cystic fibrosis

21 January 2018

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Molecular typing and colonization patterns of Aspergillus fumigatus in patients with cystic fibrosis

21 January 2018

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21 January 2018

Identifiers

DOI

10.1586/ERI.10.72

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31 July 2017

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