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Journal of Pediatric Endocrinology & Metabolism : JPEM|December 16, 2022
Clinical spectrum and diagnostic challenges of vitamin D dependent rickets type 1A (VDDR1A) caused by CYP27B1 mutation in resource limited countriesSommayya Aftab, Sabeen Abid Khan, Munir Iqbal Malik, et al.
Molecules (Basel, Switzerland)|September 23, 2022
Antibacterial, Antioxidant, and Phytotoxic Potential of Phytosynthesized Silver Nanoparticles Using Elaeagnus umbellata Fruit ExtractHafsa Zulfiqar, Muhammad Shoaib Amjad, Ansar Mehmood, et al.
Life Science Alliance|January 12, 2023
Secondary findings in a large Pakistani cohort tested with whole genome sequencingAliaksandr Skrahin, Huma Arshad Cheema, Maqbool Hussain, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|April 27, 2011
CNS neoplasms in Pakistan, a pathological perspectiveZubair Ahmad, Huma Arshad, Sheema H Hasan, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 11, 2017
Genetic analysis of fructose-1,6-bisphosphatase (FBPase) deficiency in nine consanguineous Pakistani familiesSadaqat Ijaz, Muhammad Yasir Zahoor, Muhammad Imran, et al.
Therapeutic Advances in Urology|November 16, 2020
The sclerosing Sertoli cell tumor of the testis is an extremely rare entityFaaz Salah Gomha, Kamran Hassan Bhatti, Ayad A Yousif, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|January 1, 2014
Gastrointestinal, liver and biliary tract pathology: a histopathological and epidemiological perspective from Pakistan with a review of the literatureZubair Ahmad, Huma Arshad, Saira Fatima, et al.
European Journal of Human Genetics : EJHG|December 12, 2024
Bi-allelic MYMX variants cause a syndromic congenital myopathy with recognizable facial palsy, growth restriction, and dysmorphismFatima Rahman, Luisa Marsili, Domizia Pasquetti, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|June 18, 2014
How our practice of histopathology, especially tumour pathology has changed in the last two decades: reflections from a major referral center in PakistanZubair Ahmad, Romana Idrees, Saira Fatima, et al.
Brain : a Journal of Neurology|October 8, 2025
EIPR1 variants cause a neurodevelopmental disorder with endolysosomal and dense core vesicle defectsSaikat Ghosh, Jaskaran Singh, Nadirah S Damseh, et al.
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