H
Hina Bashir
Researcher at University of Lahore
Publications - 9
Citations - 37
Hina Bashir is an academic researcher from University of Lahore. The author has contributed to research in topics: Anesthesia & Medicine. The author has an hindex of 3, co-authored 4 publications receiving 20 citations. Previous affiliations of Hina Bashir include Yahoo!.
Papers
More filters
Journal ArticleDOI
Deleterious Variants in WNT10A, EDAR, and EDA Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations.
Asia Parveen,Sher Alam Khan,Muhammad Usman Mirza,Hina Bashir,Hina Bashir,Fatima Arshad,M. M. Iqbal,Waseem Ahmad,Ahsan Wahab,Amal Fiaz,Sidra Naz,Fareeha Ashraf,Tayyaba Mobeen,Salman Aziz,Syed Shoaib Ahmed,Noor Muhammad,Nehal F. Hassib,Mostafa I. Mostafa,Nagwa E. A. Gaboon,Roquyya Gul,Saadullah Khan,Matheus Froeyen,Muhammad Shoaib,Naveed Wasif,Naveed Wasif +24 more
TL;DR: The genetic cause of 18 syndromic and non-syndromic tooth agenesis patients in six autosomal recessive and X-linked pedigrees (A-F) is explained, which expand the mutational spectrum of these unique clinical manifestations.
Journal ArticleDOI
A novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulations
Asia Parveen,Asia Parveen,Muhammad Usman Mirza,Michiel Vanmeert,Javed Akhtar,Hina Bashir,Saadullah Khan,Saqib Shehzad,Matheus Froeyen,Wasim Ahmed,Muhammad Ansar,Naveed Wasif,Naveed Wasif,Naveed Wasif +13 more
TL;DR: Pathogenic mutations in the Cyclin and CBS Domain Divalent Metal Cation Transport Mediator 4 (CNNM4) magnesium transporter protein have been reported as the leading cause of this anomaly.
Journal ArticleDOI
A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family.
Sher Alam Khan,Muhammad Adnan Khan,Nazif Muhammad,Hina Bashir,Niamat Khan,Noor Muhammad,Rüstem Yilmaz,Saadullah Khan,Naveed Wasif,Naveed Wasif,Naveed Wasif +10 more
TL;DR: A novel nonsense sequence variant c.1192C > T (p.Gln398*) is the sixth disease-causing variant in SLC24A4, which extends its mutation spectrum and confirms the role of this gene in the morphogenesis of human tooth enamel.
Journal ArticleDOI
Novel homozygous nonsense variant in MLPH causing Griscelli syndrome type 3 in a consanguineous Pakistani family.
Naveed Wasif,Asia Parveen,Hina Bashir,Fareeha Ashraf,Ehtasham Ali,Kashif Raza Khan,Amina Arif +6 more
TL;DR: To date, three GS forms (GS-1, GS-2 and GS-3) are clinically characterized by silvery gray hair and the accumulation of melanin pigment in the form of large bundles in the hair shaft when microscopically observed.
Journal ArticleDOI
People Treated Upper Limb Surgery Comparing Positive Patient Outcomes with Regional Anesthetic vs General Anesthesia
Tahmina Karim Bhatti,Muhammad Fayyaz,Ranna Musarrat,Hina Bashir,Attaullah Bangulzai,Syed Aqeel Akbar Shah Gillani +5 more
TL;DR: For upper limb procedures, RA gives higher client experience than GA, as well as the longer time of analgesia in addition a shorter hospital admittance.