Inheritance and susceptibility to dental caries: A community-based study von Khan, Saima

Volltext

Clinical efficacy of a novel lipid-based Thymoquinone gel: A two-arm, single-blinded, and randomized study von Khan, Saima Y, Ahmad, Imran

Volltext

Effectiveness of Audiovisual Distraction Technique and Filmed Modeling on Anxiety and Fear in Pediatric Dental Patients von Khan, Saima Y, Jamil, Faiza, Jindal, Mahendra K

Volltext

An Exploratory Study of Consanguinity and Dental Developmental Anomalies von Khan, Saima Y

Volltext

Quantification of Color Variation of Various Esthetic Restorative Materials in Pediatric Dentistry von Kumar, Vinod, Khan, Saima Y, Jindal, Mahendra K, Varshney, Pranshu, Azim, Yasser, Bhardwaj, Aditi

Volltext

Satisfaction of Primary Caregiver with the Dental Treatment by Silver Diammine Fluoride during COVID-19 Pandemic von Javed, Faraha, Khan, Saima Y., Sharma, Manoj Kumar

Volltext

SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis von Anwar, Saima, Riazuddin, Saima, Ahmed, Zubair M, Tasneem, Saba, Ateeq-ul-Jaleel, Khan, Shahid Y, Griffith, Andrew J, Friedman, Thomas B, Riazuddin, Sheikh

Volltext

Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79 von Rehman, Atteeq Ur, Morell, Robert J., Belyantseva, Inna A., Khan, Shahid Y., Boger, Erich T., Shahzad, Mohsin, Ahmed, Zubair M., Riazuddin, Saima, Khan, Shaheen N., Riazuddin, Sheikh, Friedman, Thomas B.

Volltext

Molecular Basis of DFNB73: Mutations of BSND Can Cause Nonsyndromic Deafness or Bartter Syndrome von Riazuddin, Saima, Anwar, Saima, Fischer, Martin, Ahmed, Zubair M., Khan, Shahid Y., Janssen, Audrey G.H., Zafar, Ahmad U., Scholl, Ute, Husnain, Tayyab, Belyantseva, Inna A., Friedman, Penelope L., Riazuddin, Sheikh, Friedman, Thomas B., Fahlke, Christoph

Volltext

A missense allele of PEX5 is responsible for the defective import of PTS2 cargo proteins into peroxisomes von Ali, Muhammad, Khan, Shahid Y., Rodrigues, Tony A., Francisco, Tânia, Jiao, Xiaodong, Qi, Hang, Kabir, Firoz, Irum, Bushra, Rauf, Bushra, Khan, Asma A., Mehmood, Azra, Naeem, Muhammad Asif, Assir, Muhammad Zaman, Ali, Muhammad Hassaan, Shahzad, Mohsin, Abu-Amero, Khaled K., Akram, Shehla Javed, Akram, Javed, Riazuddin, Sheikh, Riazuddin, Saima, Robinson, Michael L., Baes, Myriam, Azevedo, Jorge E., Hejtmancik, J. Fielding, Riazuddin, S. Amer

Volltext

Phenotypic Variability Associated with the D226N Allele of IMPDH1 von Ali, Shahbaz, PhD, Khan, Shahid Y., PhD, Naeem, Muhammad Asif, PhD, Khan, Shaheen N., PhD, Husnain, Tayyab, PhD, Riazuddin, Saima, PhD, Ayyagari, Radha, PhD, Riazuddin, Sheikh, PhD, Hejtmancik, J. Fielding, MD, PhD, Riazuddin, S. Amer, PhD

Volltext

Prevalence of Methylphenidate Misuse in Medical Colleges in Pakistan: A Cross-sectional Study von Javed, Nismat, Ahmed, Fatimah, Saeed, Sikandar, Amir, Raham, Khan, Hadia Y, Iqbal, Saima P

Volltext

Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3 von KHAN, Shahid Y, RIAZUDDIN, Saima, RIAZUDDIN, Sheikh, TARIQ, Muhammad, ANWAR, Saima, SHABBIR, Muhammad I, AMER RIAZUDDIN, S, KHAN, Shaheen N, HUSNAIN, Tayyab, AHMED, Zubair M, FRIEDMAN, Thomas B

Volltext

Assessment of River Water Quality During a Religious Mass Bathing Festival at Sangam, Prayagraj von Lall, Anurag Samson, Chattree, Amit, Thomas, Tarence, Khan, Saima Habib, Pandey, Avinash Kumar, Mani, Jyoti Vandana

Volltext

A missense allele of PEX5 is responsible for the defective import of PTS2 cargo proteins into peroxisomes von Ali, Muhammad, Khan, Shahid Y, Rodrigues, Tony A, Francisco, Tania, Jiao, Xiaodong, Qi, Hang, Kabir, Firoz, Irum, Bushra, Rauf, Bushra, Khan, Asma A, Mehmood, Azra, Naeem, Muhammad Asif, Assir, Muhammad Zaman, Ali, Muhammad Hassaan, Shahzad, Mohsin, Abu-Amero, Khaled K, Akram, Shehla Javed, Akram, Javed, Riazuddin, Sheikh, Riazuddin, Saima, Robinson, Michael L, Baes, Myriam, Azevedo, Jorge E, Hejtmancik, J. Fielding, Riazuddin, S. Amer

Volltext

Adsorptive Separation Studies of β-Carotene from Methyl Ester Using Mesoporous Carbon Coated Monolith von Muhammad, M., Choong, T. S. Y., Ali Khan, Moonis

Volltext

Diet and hypertension: Food to eat and to avoid von Ullah, Raza, Sarir, Saima, Khan, Younas, Ahmad, Shakeel, Alsawalqa, Rula Odeh, Ullah, Shafqat, Sajjad, Muhammad

Volltext

Whole genome sequencing data of multiple individuals of Pakistani descent von Khan, Shahid Y., Ali, Muhammad, Lee, Mei-Chong W., Ma, Zhiwei, Biswas, Pooja, Khan, Asma A., Naeem, Muhammad Asif, Riazuddin, Saima, Riazuddin, Sheikh, Ayyagari, Radha, Hejtmancik, J. Fielding, Riazuddin, S. Amer

Volltext

Mutations of human TMHS cause recessively inherited non-syndromic hearing loss von Shabbir, M I, Ahmed, Z M, Khan, S Y, Riazuddin, Saima, Waryah, A M, Khan, S N, Camps, R D, Ghosh, M, Kabra, M, Belyantseva, I A, Friedman, T B, Riazuddin, Sheikh

Volltext

Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus von Khan, Shahid Y., Ahmed, Zubair M., Shabbir, Muhammad I., Kitajiri, Shin-ichiro, Kalsoom, Saeeda, Tasneem, Saba, Shayiq, Sara, Ramesh, Arabandi, Srisailpathy, Srikumari, Khan, Shaheen N., Smith, Richard J.H., Riazuddin, Saima, Friedman, Thomas B., Riazuddin, Sheikh

Volltext