Bone Mineral Density in Cystic Fibrosis Patients with the CFTR I1234V Mutation in a Large Kindred Family Is Associated with Pancreatic Sufficiency

Autor: Atqah Abdul Wahab, M. Hammoudeh, Mona Allangawi, Fawziya Al-Khalaf, Prem Chandra

Publikováno v: International Journal of Rheumatology, Vol 2014 (2014)

Objectives. To study bone mineral density (BMD) in cystic fibrosis (CF) children and adults with the CFTR I1234V mutation associated with pancreatic sufficiency. Methods. Lumbar spine, total hip, and whole-body mineral density were measured by dual-e

Externí odkaz: https://doaj.org/article/362ef5a9cabd41a887752746406391b6

Variability of ß-lactamase resistance Pseudomonas aeruginosa genes infecting patients with cystic fibrosis

Autor: Atqah Abdul Wahab, Mazen A Sid Ahmed, Emad Ibrahim, Ali A. Sultan, Jana Jass

Publikováno v: Respiratory infections and bronchiectasis.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::95cbc0ecc7809e9b95d309a53e623dbc
https://doi.org/10.1183/13993003.congress-2021.pa2353

Molecular Identification and Susceptibility Pattern of ClinicalNocardiaSpecies: Emergence ofNocardia crassostreaeas an Agent of Invasive Nocardiosis

Autor: Mona Allangawi, Ahmed AlMuzrkchi, Anand Deshmukh, Atqah Abdul Wahab, Saad J. Taj-Aldeen, Sanjay Doiphode, Corné H. W. Klaassen, Jacques F. Meis

Publikováno v: Canadian Journal of Infectious Diseases and Medical Microbiology, Vol 24, Iss 2, Pp e33-e38 (2013)
Scopus-Elsevier
Canadian Journal of Infectious Diseases & Medical Microbiology, 24, 2, pp. e33-e38
Canadian Journal of Infectious Diseases & Medical Microbiology, 24, e33-e38

BACKGROUND:Nocardiaspecies are rare, opportunistic organisms that cause disease in both immunocompetent and immunocompromised individuals.OBJECTIVE: To investigate the clinical presentations of variousNocardiainfections based on the 16S ribosomal RNA

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6a1817f3a2c5a0eae2c8cd4f99bfc18
https://doi.org/10.1155/2013/256025

Persistence ofcandida dubliniensisin the lower airways of cystic fibrosis patients

Autor: Saad J. Taj-Aldeen, Teun Boeckhout, Atqah Abdul Wahab, Husam M. Salah, Anna Kolecka

Publikováno v: 7.3 Cystic Fibrosis.

Background: Candida dubliniesis is emerging yeast in the respiratory tract of patients with cystic fibrosis (CF). Aims and objectives: To determine the frequency of C . dubliniensis recovered from lower respiratory samples of CF patients and compare

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::72cb353461fdda9f7f214af519d98e5b
https://doi.org/10.1183/13993003.congress-2015.pa2058

High prevalence of Candida dubliniensis in lower respiratory tract secretions from cystic fibrosis patients may be related to increased adherence properties

Autor: Atqah Abdul Wahab, Jonathan S. Finkel, Mei ElGindi, Saad J. Taj-Aldeen, Anna Kolecka, Teun Boekhout

Publikováno v: International Journal of Infectious Diseases, 24, 14-9. Elsevier B.V.

Summary Objectives We identified Candida spp isolated from lower respiratory tract secretions obtained from cystic fibrosis (CF) patients, by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS), with the aim of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc312f90f3023472e95f2d100b4a48fc
https://pure.knaw.nl/portal/en/publications/4dd56b50-80ad-4da9-ae2a-c6a19dbf2157