Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Muna Al Bimani"'
Autor:
Mohamed S. Al Riyami, Intisar Al Alawi, Badria Al Gaithi, Anisa Al Maskari, Naifain Al Kalbani, Nadia Al Hashmi, Aisha Al Balushi, Maryam Al Shahi, Suliman Al Saidi, Muna Al Bimani, Fahad Al Hatali, Holly Mabillard, John A. Sayer
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 9, Pp n/a-n/a (2023)
Abstract Background Nephrotic syndrome (NS) is one of the most common kidney disorders seen by pediatric nephrologists and is defined by the presence of heavy proteinuria (>3.5 g/24 h), hypoalbuminemia (
Externí odkaz:
https://doaj.org/article/bc1175343931410fb57746ded5631b6d
Autor:
Sumaya Al Oraimi, Khoula Al Shidhani, Hasina Al Harthi, Suaad Al Sinani, Nasser Al Busaidi, Muna Al Bimani, Qasem Al Salmi, Hussein Al Kindi
Publikováno v:
Oman Medical Journal, Vol 37, Iss 6, Pp e444-e444 (2022)
Objectives: To describe the demographic distribution of cystic fibrosis (CF) in Omani children, estimate the national prevalence, and provide updated mutational panels of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Methods: W
Externí odkaz:
https://doaj.org/article/caf6c221582e4acd8551f55e58864cad
Autor:
Hussein Al-Kindy, Muna Al-Bimani, Mariam Al-Nabhani, Allal Ouhtit, Ishita Gupta, Qasim Al-Salmi
Publikováno v:
Journal of Molecular Biomarkers & Diagnosis.
Introduction: Cystic fibrosis (CF) is the most common lethal autosomal recessive disorder among Caucasians (1: 3,000). In CF, the CFTR gene is frequently mutated, with ΔF508del being the largely common mutation in Caucasians. Our preliminary pilot s