Further Evidence of a Recessive Variant in COL1A1 as an Underlying Cause of Ehlers–Danlos Syndrome: A Report of a Saudi Founder Mutation

by Ahmad Almatrafi, Jamil A. Hashmi, Fatima Fadhli, Asma Alharbi, Sibtain Afzal, Khushnooda Ramzan, Sulman Basit
Published 2020-12-01

A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients

by Sibtain Afzal, Khushnooda Ramzan, Sajjad Ullah, Salma M. Wakil, Arshad Jamal, Sulman Basit, Ahmed Bilal Waqar
Published 2020-01-01

Involvement of Muscarinic Receptors in Hypotensive and Diuretic Effects of Aqueous Soluble Fraction from Asphodelus tenuifolius Cav.

by Waqas Younis, Alamgeer, V. B. Schini-Kerth, Samara Requena Nocchi, Denise Brentan Silva, Priscila de Souza, Ishfaq Ali Bukhari, Fahim Vohra, Sibtain Afzal, Arquimedes Gasparotto Junior
Published 2021-01-01

Prevalence of UDP-glucuronosyltransferase polymorphisms (UGT1A6∗2, 1A7∗12, 1A8∗3, 1A9∗3, 2B7∗2, and 2B15∗2) in a

by Khalid M. Alkharfy, Basit L. Jan, Sibtain Afzal, Fahad I. Al-Jenoobi, Abdullah M. Al-Mohizea, Saleh Al-Muhsen, Rabih Halwani, Mohammad K. Parvez, Mohammed S. Al-Dosari
Published 2017-02-01

Three common single-nucleotide variants in the promoter region of thymic stromal lymphopoietin cytokine are not associated with asthma prevalence in a Saudi Arabian population

by Maha Fahad Alenazy, Alejandro Vazquez-Tello, Rosan Kenana, Fatemeh Saheb Sharif-Askari, Areej Rashid Alkahtani, Amer Jamhawi, Sibtain Afzal, Roua Al-Kufiedy, Mohamed-Hani Temsah, Abeer Al-Masri, Fahad Alsohaime, Ayman Al-Eyadhy, Adel M Zakri, Elaref Ratemi, Saleh Al-Muhsen, Rabih Halwani
Published 2020-01-01