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Journal of Cardiothoracic and Vascular Anesthesia|August 2, 2020
Handheld Point-of-Care Ultrasound Probes: The New Generation of POCUSYanick Baribeau, Aidan Sharkey, Omar Chaudhary, et al.Pakistan Journal of Medical Sciences|March 16, 2026
Congenital anomalies prevalent in rural population of Dera Ismail Khan, Pakistan: Ethnic inequalities and biodemographic attributesMuhammad Asghar Khan, Qumar Zaman, Saima Naz, et al.Pakistan Journal of Medical Sciences|June 15, 2026
Spectrum and epidemiology of neurological disorders and neuromuscular anomalies in pediatric population of Sialkot, PakistanHamna Shahid, Aneeta Kumari, Urwa Hafeez, et al.Cureus|June 22, 2026
Caught in a Cocoon: Operative Release of Primary Sclerosing Encapsulating Peritonitis With Endoscopic Management of Early Postoperative Duodenojejunal IntussusceptionChun Pui Joshua Wong, Sajid Malik, Samina Alim, et al.Preparative Biochemistry & Biotechnology|August 31, 2025
Lactones as promising biofilm inhibitors: disrupting bacterial communication for Next-Gen therapiesShivani Chaturvedi, Tanisha Singh, Huma Fatima, et al.Asian Cardiovascular & Thoracic Annals|June 29, 2021
Role of trans-radial band protocols in radial artery occlusion: Randomized trialNasir Rahman, Azmina Artani, Farhala Baloch, et al.Clinical Kidney Journal|April 17, 2015
Immune profile of IgA-dominant diffuse proliferative glomerulonephritisEric Wallace, Nicolas Maillard, Hiroyuki Ueda, et al.Journal of Medical Genetics|November 12, 2017
Homozygous mutation in CEP19, a gene mutated in morbid obesity, in Bardet-Biedl syndrome with predominant postaxial polydactylyEsra Yıldız Bölükbaşı, Sara Mumtaz, Muhammad Afzal, et al.American Journal of Medical Genetics. Part A|June 22, 2017
Progressive SCAR14 with unclear speech, developmental delay, tremor, and behavioral problems caused by a homozygous deletion of the SPTBN2 pleckstrin homology domainEsra Yıldız Bölükbaşı, Muhammad Afzal, Sara Mumtaz, et al.European Journal of Human Genetics : EJHG|November 15, 2007
Fifth finger camptodactyly maps to chromosome 3q11.2-q13.12 in a large German kindredSajid Malik, Jörg Schott, Julia Schiller, et al.Pageof 18