Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Hanaa Banjar"'
Publikováno v:
Frontiers in Nutrition, Vol 9 (2022)
BackgroundChildren with cystic fibrosis (CF) are expected to have suboptimal serum vitamin D status and altered gut microbiota. The altered gut microbiota is hypothesized to have a pro-inflammatory effect that further complicates the existing respira
Externí odkaz:
https://doaj.org/article/fe2b69d7b5774cfca535110329000666
Autor:
Majdy M. Idrees, Sarfraz Saleemi, M Ali Azem, Saleh Aldammas, Manal Alhazmi, Javid Khan, Abdulgafour Gari, Maha Aldabbagh, Husam Sakkijha, Abdulla Aldalaan, Khalid Alnajashi, Waleed Alhabeeb, Imran Nizami, Amjad Kouatli, May Chehab, Omar Tamimi, Hanaa Banjar, Tarek Kashour, Antonio Lopes, Omar Minai, Paul Hassoun, Qadar Pasha, Eckhard Mayer, Ghazwan Butrous, Sastry Bhagavathula, Stefano Ghio, John Swiston, Adel Boueiz, Adriano Tonelli, Robert D. Levy, Marius Hoeper, Rober D. Levy
Publikováno v:
Annals of Thoracic Medicine, Vol 9, Iss 5, Pp 1-15 (2014)
The Saudi Association for Pulmonary Hypertension (previously called Saudi Advisory Group for Pulmonary Hypertension) has published the first Saudi Guidelines on Diagnosis and Treatment of Pulmonary Arterial Hypertension back in 2008. [1] That guideli
Externí odkaz:
https://doaj.org/article/d8cd5a2237ef4764b479a57fa53569e1
Autor:
Mais AlAshgar, Afrah Ghawi, Lama Abanemai, Hanaa Banjar, Ibrahim Al-Mogarri, Sami Alhaider, Abdullah Hejazi, Sharouk Khanjar, Abdulrahaman Alfadhel, Areej AlFattani, Hanan Alomran, Alaa Alghazzi
Publikováno v:
International Journal of Pediatrics and Adolescent Medicine. 9:108-112
Introduction Bacterial infections in CF patients are common and start early in life. The prognosis of the disease is substantially dependent on chronic respiratory infection and inflammation. Pseudomonas aeruginosa (PA) infection or chronic colonizat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98f473c2e1bfba68f4e17addb497b22b
https://doi.org/10.1016/j.ijpam.2021.07.001
https://doi.org/10.1016/j.ijpam.2021.07.001
Autor:
Hanaa Banjar, Reem Ghomraoui
Publikováno v:
International Journal of Dentistry & Oral Health. :1-4
Introduction: Previous data showed that dental caries is common in the Saudi general population as well as in the Cystic fibrosis patients. Objectives: to identify the correlation of dental caries severity with cystic fibrosis (CFTR) gene mutations i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8950480126c2995d73b8d8a874b3df1d
https://doi.org/10.46715/ijdoh2021.07.1000105
https://doi.org/10.46715/ijdoh2021.07.1000105
Autor:
Hanaa Banjar, Talal AlMaghamsi, Ibrahim Al-Mogarri, Sara AlKaf, Sami Alhaider, Nabil Moghrabi, Abdulaziz Al-Enazi, Imran Nizami
Publikováno v:
International Journal of Pediatrics and Adolescent Medicine, Vol 8, Iss 1, Pp 25-28 (2021)
International Journal of Pediatrics & Adolescent Medicine
International Journal of Pediatrics & Adolescent Medicine
Introduction Cystic fibrosis (CF) has been reported before in Saudi Arabia and the Gulf area. It has been found that screening for 10 most common cystic fibrosis transmembrane conductance regulator (CFTR) mutations can detect 80% of positive CFTR cas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2ecd1e549aa6efe19cf0a8a793c9862
http://www.sciencedirect.com/science/article/pii/S2352646719302182
http://www.sciencedirect.com/science/article/pii/S2352646719302182
The first report on immunoglobulins A, E, G and M levels in cystic fibrosis patients in Saudi Arabia
Publikováno v:
Saudi Journal of Biological Sciences, Vol 27, Iss 10, Pp 2617-2621 (2020)
Saudi Journal of Biological Sciences
Saudi Journal of Biological Sciences
Background Previous reports have shown that pulmonary and systemic hypergamma-globulinemia in CF patients is a reflection of chronic pulmonary infection. Infection with Pseudomonas aeruginosa is known to have major prognostic significance in patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64db657a39a4f9f0ebc13c1a3d118038
http://www.sciencedirect.com/science/article/pii/S1319562X20302217
http://www.sciencedirect.com/science/article/pii/S1319562X20302217
Publikováno v:
Global Journal of Rare Diseases. :015-021
Double homozygous mutation with the presence of double mutations in each allele is a very rare phenomenon with only 2 reports that have described this phenomenon in the medical literature.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f4c29efa16ebe6a95f5af58592f9847
https://doi.org/10.17352/2640-7876.000023
https://doi.org/10.17352/2640-7876.000023
Autor:
Sami Alhaider, Mohammad Chaballout, Imran Nizami, Ali Al-Nakhli, Hanaa Banjar, Hadeel Al-Ghamdi, Ibrahim Al-Mogarri, Rawia Raja, Kawthar Karkour
Publikováno v:
International Journal of Pediatrics and Adolescent Medicine, Vol 7, Iss 2, Pp 83-87 (2020)
Introduction Studies have shown that pulmonary exacerbations in cystic fibrosis (CF) patients are associated with respiratory viruses. The most common agent causing viral infections in patients with CF before the age of 3 years is respiratory syncyti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8383f3732a66ca4601729695e8af03d2
http://www.sciencedirect.com/science/article/pii/S2352646718302138
http://www.sciencedirect.com/science/article/pii/S2352646718302138
Autor:
Al-Shammari A, Al-Eid M, Ghomraoui R, Hanaa Banjar, Firas Ghomraoui, Al-Mulhim Fa, Al-Ghuneim L
Publikováno v:
Asploro Journal of Pediatrics and Child Health. 2:37-43
Introduction: Cholelithiasis has been reported in 12%-24% of Cystic Fibrosis (CF) patients, and is usually made up of cholesterol gallstones. These abnormalities are frequently asymptomatic and can include intra and extrahepatic ducts, gallbladder th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ca45b02eb991d515430c9adc570d32d
https://doi.org/10.36502/2020/asjpch.6155
https://doi.org/10.36502/2020/asjpch.6155
Autor:
Ali Al-Nakhli, Hend D. Alqahtani, Hanaa Banjar, Hanan S. Alamer, Kawthar Karkour, Rawia Raja, Waad Al-wgait, Waseem Yasin
Publikováno v:
International Journal of Pediatrics & Adolescent Medicine
International Journal of Pediatrics and Adolescent Medicine, Vol 7, Iss 4, Pp 186-190 (2020)
International Journal of Pediatrics and Adolescent Medicine, Vol 7, Iss 4, Pp 186-190 (2020)
Introduction Methicillin-resistant Staphylococcus aureus infections have been increasingly reported in patients with cystic fibrosis (CF) who have progressive deterioration in their pulmonary function. Objectives To determine the prevalence of MRSA i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5850eac8c6a478a7b76c03b93d2ef982
http://europepmc.org/articles/PMC7729253
http://europepmc.org/articles/PMC7729253