Results 31 to 40 of about 123,204 (125)

Immunisation in the current management of cystic fibrosis patients. [PDF]

, 2005
Although no special recommendations exist, clearly patients with cystic fibrosis (CF) can benefit from immunisation. We reviewed the literature regarding vaccination in CF and other chronic diseases.
Ciofu, Oana, Dab, Isi, D\uf6ring, Gerd, Bush, Andrew, European Cystic Fibrosis Society (ECFS) Vaccination Group, Adam, Georgios, Lang, Alo\uefs B., Döring, Gerd, Malfroot, Anne, Lang, Aloïs B., Lang, Aloïs B, Knoop, Christiane, Van Damme, Pierre   +12 more
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Foetal disruptive brain injuries: Diagnosing the underlying pathogenetic mechanisms with cranial ultrasonography

Developmental Medicine &Child Neurology, Volume 67, Issue 11, Page 1383-1408, November 2025.
Plain language summary: https://onlinelibrary.wiley.com/doi/10.1111/dmcn.16431 Abstract Antenatal destructive events affecting the central nervous system of the foetus lead to disruptive brain lesions that are often associated with impaired neurodevelopment.
Ana Alarcón, Nuria Carreras, Tobias Muehlbacher, Dídac Casas‐Alba, Roberta Arena, Paola Roca‐Llabrés, Juan Navarro‐Morón, Linda S. de Vries, Paul Govaert, the EurUS.Brain group, Thais Agut, Roberta Arena, Ana Alarcón, Juan Arnáez, Marco Bartocci, Isabel Benavente‐Fernández, María Carmen Bravo, Fernando Cabañas, Nuria Carreras, Olivier Claris, Jeroen Dudink, Monica Fumagalli, Alfredo García‐Alix, Paul Govaert, Sandra Horsch, Simón Lubián, Tobias Muehlbacher, Alessandro Parodi, Adelina Pellicer, Luca Ramenghi, Charles C. Roehr, Simone Schwarz, Sylke Steggerda, Eva Valverde   +33 more
wiley   +1 more source

A metagenomic approach to characterize temperate bacteriophage populations from Cystic Fibrosis and non-Cystic Fibrosis bronchiectasis patients [PDF]

, 2015
Pseudomonas aeruginosa (Pa), normally a soil commensal, is an important opportunistic pathogen in Cystic Fibrosis (CF) and non-Cystic Fibrosis Bronchiectasis (nCFBR).
Bourke, Stephen, Smith, Darren L., Anthony eDe Soyza, Cowley, Lauren A., Perry, J. D. (John), Holt, Giles S., Francesca Louise Claire Everest, Stephen eBourke, Darren L. Smith, Tariq, M. A. (Mohammad), Smith, Darren, Stephen eCummings, Holt, Giles, Clare V. Lanyon, Cowley, Lauren, Jeremy J Barr, Bourke, Stephen J., Barr, Jeremy J., Mohammad Adnan Tariq, Bridge, Simon H., Cummings, Stephen, Perry, John, Audrey Perry, Jeremy J. Barr, Barr, Jeremy, Francesca L. C. Everest, Stephen J. Bourke, Bridge, Simon, Simon H. Bridge, Audrey ePerry, Anthony De Soyza, Simon Harwood Bridge, Stephen P. Cummings, John D. Perry, Tariq, Mohammad, Darren Lee Smith, Everest, Francesca, John D Perry, Giles Samuel Holt, Lauren A. Cowley, Lanyon, Clare, Mohammad A. Tariq, Everest, F. L. C. (Francesca), Giles S. Holt, de Soyza, Anthony, Perry, Audrey, Lauren eCowley, Clare Veronica Lanyon   +47 more
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Atypical Manifestations of Old World Cutaneous Leishmaniasis: A Systematic Review and Clinical Atlas of Unusual Clinical and Specific Anatomical Presentations

Health Science Reports, Volume 8, Issue 9, September 2025.
ABSTRACT Background and Aims Cutaneous leishmaniasis (CL) represents the most common form of leishmaniasis. It imposes a significant medical burden due to long‐lasting ulcers and disfiguring scars, underscoring the need for comprehensive CL control strategies, particularly in endemic regions.
Bahareh Abtahi‐Naeini, Seyed Naser Emadi, Zabihollah Shahmoradi, Mahsa Pourmahdi‐Boroujeni, Ali Saffaei, Fereshte Rastegarnasab   +5 more
wiley   +1 more source

Health economic modelling in Cystic Fibrosis: a systematic review [PDF]

, 2019
INTRODUCTION: Cystic Fibrosis (CF) is a heritable chronic condition. Due to the genetic and progressive nature of CF, a number of interventions are available for the condition.
Sach, Tracey, Carr, Siobhan, Turner, David, Archangelidi, Olga, Bhadhuri, Arjun, Whitty, Jennifer A., Bilton, Diana, Whitty, Jennifer A, Mohindru, Bishal   +8 more
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Osseous hydatidosis - A diagnostic mimic and a therapeutic challenge: Clinicopathological and radiological features of 21 cases from India

Indian Journal of Pathology and Microbiology
Background: Bone constitutes a rare site of involvement in hydatid disease, associated with a diagnostic challenge. Objective: The present study is an analysis of the clinicopathological features of osseous hydatidosis, emphasizing on its diverse ...
Shantveer G. Uppin, Monalisa Hui, Bharat Rekhi, K. R. Harsha Vardhana, Nirmala Jambhekar, Rajeev Reddy   +5 more
doaj   +1 more source

Targeted Therapies for Slow‐Flow Vascular Malformations

Australasian Journal of Dermatology, Volume 66, Issue 3, Page 142-151, May 2025.
ABSTRACT Advances in genetic sequencing technologies have enabled the identification of key activating somatic variants in cellular signalling pathways involved in the pathogenesis of vascular malformations. Given that these genetic variants are also implicated in the pathogenesis of several cancers, the repurposing of targeted therapies developed in ...
Grace X. Li, Deshan F. Sebaratnam, James P. Pham   +2 more
wiley   +1 more source

An exploration of the factors involved in lifestyle decisions in young people with cystic fibrosis using decision making vignettes, and the role of perceived risk in infection [PDF]

, 2010
This study explored the factors involved in lifestyle decision making in young people with Cystic Fibrosis, specifically the role of infection risk. Certain pathogens present a high risk of infection to people with Cystic Fibrosis, and can significantly
Brash, Lisa Marie
core   +5 more sources

Brain MRI findings in paediatric genetic disorders associated with white matter abnormalities

Developmental Medicine &Child Neurology, Volume 67, Issue 2, Page 186-194, February 2025.
Plain language summary: https://onlinelibrary.wiley.com/doi/10.1111/dmcn.16100 This original article is commented by Wolf et al. on pages 143–144 of this issue. Abstract Aim To describe the specific brain magnetic resonance imaging (MRI) patterns of the paediatric genetic disorders associated with white matter abnormalities in Northern Finland.
Jaakko H. Oikarainen, Oula A. Knuutinen, Salla M. Kangas, Elisa J. Rahikkala, Tytti M.‐L. Pokka, Jukka S. Moilanen, Reetta M. Hinttala, Päivi M. Vieira, Johanna M. Uusimaa, Maria H. Suo‐Palosaari   +9 more
wiley   +1 more source

Cystic fibrosis [PDF]

, 2004
In the 1930s, when cystic fibrosis (CF) was first clearly recognised, it was a disorder that inevitably led to death in early childhood from respiratory failure and malnutrition.

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