scholarly journals A case report of a cystic fibrosis patient with repeated isolation of Trichosporon mycotoxinivorans identified by a novel short-extraction method

2016 ◽  
Vol 16 (1) ◽  
Author(s):  
Daniel Goldenberger ◽  
Vladimira Hinić ◽  
Spasenija Savic Prince ◽  
Michael Tamm ◽  
Anna-Maria Balestra ◽  
...  
2020 ◽  
Vol 2 ◽  
pp. 10-10
Author(s):  
Françoise Le Pimpec-Barthes ◽  
Giuseppe Mangiameli ◽  
Ciprian Pricopi ◽  
Alex Arame ◽  
Anne Hernigou ◽  
...  

2021 ◽  
Vol 9 ◽  
Author(s):  
Giulia Baresi ◽  
Mauro Giacomelli ◽  
Daniele Moratto ◽  
Marco Chiarini ◽  
Immacolata Claudia Conforti ◽  
...  

Since the beginning of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic, data registered in the European countries revealed increasing cases of infection in cystic fibrosis (CF) patients. In the course of this pandemic, we enrolled 17 CF patients for a study evaluating inflammatory markers. One of them developed COVID-19, giving us the possibility to analyze inflammatory markers in the acute phase as compared to levels detected before and after the infectious episode and to levels measured in the other CF patients enrolled to the study who did not experience COVID-19 and 23 patients referred to our center for SARS-CoV-2 infection.


2020 ◽  
Vol 2 (2) ◽  
Author(s):  
Octavio Carretero-Vicario ◽  
Irene Taravillo ◽  
Laura Corbella ◽  
Mercedes Catalan ◽  
Cristina Garfia ◽  
...  

2018 ◽  
Vol 18 (1) ◽  
Author(s):  
Vanitha Mariappan ◽  
Surendran Thavagnanam ◽  
Kumutha Malar Vellasamy ◽  
Cindy Ju Shuan Teh ◽  
Nadia Atiya ◽  
...  

2008 ◽  
Vol 15 (5) ◽  
pp. 237-239 ◽  
Author(s):  
Dimas Mateos Corral ◽  
Allan L Coates ◽  
Yvonne CW Yau ◽  
Raymond Tellier ◽  
Mindy Glass ◽  
...  

Burkholderia pseudomalleiis a pathogen identified with increasing frequency in the respiratory tracts of cystic fibrosis (CF) patients from endemic areas such as Southeast Asia and northern Australia. The following report describes the first known reported case in a CF patient from the Caribbean attending a North American CF clinic.


1997 ◽  
Vol 111 (8) ◽  
pp. 760-762 ◽  
Author(s):  
Elizabeth C. Adam ◽  
Dietlind U. Schumacher ◽  
Udo Schumacher

AbstractThe ciliary beat frequency measurements taken from a nasal polyp from a cystic fibrosis patient were similar to that of the control nasal polyps. The addition of a ciliotoxic lectin produced byPseudomonas aeruginosastopped the beating of the cilia as in the controls. This reaction could be blocked by the pre-incubation of the lectin with its inhibitor fucose. As in the control, the addition of fucose after the cilia had slowed resulted in a return to normal ciliary beating within 24 hours. This shows that the delta F508 CF mutation observed in this patient does not affect ciliary beating and suggests that treatment with fucose in the early stages of aPseudomonas aeruginosainfection could be advantageous for cystic fibrosis patients.


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