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A Recurrent Nonsense Mutation in NECTIN4 Underlying Ectodermal Dysplasia-Syndactyly Syndrome with a Novel Phenotype in a Consanguineous Kashmiri Family.
Ali G, Sadia S, Ain-Ul-Batool S, Azeem Z, Awan NB, Kazmi SAR, Ur-Rehman Z, Anjum Z, Ur-Rehman F, Wali A, Khan K, Zaman N, Ayub M, Sajid M, Hassan N. Ali G, et al. Among authors: ur rehman f. Genet Res (Camb). 2023 Oct 4;2023:9999660. doi: 10.1155/2023/9999660. eCollection 2023. Genet Res (Camb). 2023. PMID: 37829154 Free PMC article.
Nanocrytals-Mediated Oral Drug Delivery: Enhanced Bioavailability of Amiodarone.
Awan AM, Farid A, Shah SU, Khan D, Ur Rehman F, Dar MJ, Iftikhar T, Ghazanfar S, Galanakis CM, Alamri AS, Asdaq SMB, Shah KU. Awan AM, et al. Among authors: ur rehman f. Pharmaceutics. 2022 Jun 18;14(6):1300. doi: 10.3390/pharmaceutics14061300. Pharmaceutics. 2022. PMID: 35745871 Free PMC article.
Investigating The Role of Inflammatory Markers at Admission in Defining the Severity of Moderate-to-Critical COVID-19: A Cross-Sectional Analysis.
Jawad Zaidi SM, Awan MH, Bhatti HW, Sabir S, Ahmed S, Arshad I, Khalid MA, Ur Rehman F. Jawad Zaidi SM, et al. Among authors: ur rehman f. J Community Hosp Intern Med Perspect. 2022 Apr 12;12(2):1-5. doi: 10.55729/2000-9666.1029. eCollection 2022. J Community Hosp Intern Med Perspect. 2022. PMID: 35712690 Free PMC article.
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