Showing results (41-50 of 51) with videos related to
Sort By:
Pageof 6
Journal of Molecular Medicine (Berlin, Germany)|April 6, 2006
Localization of a novel autosomal recessive nonsyndromic hearing impairment locus DFNB65 to chromosome 20q13.2-q13.32Aamira Tariq, Regie Lyn P Santos, Mohammad Nasim Khan, et al.Cureus|January 9, 2023
Patterns of Functional Gastrointestinal Disorders Among Children in Makkah City: A Single Institutional ExperienceHisham Alkhuzaei, Mohammed A Almatrafi, Wed Alqahtani, et al.The American Journal of Tropical Medicine and Hygiene|December 1, 2004
Cerebral metabolic reduction in severe malaria: fluorodeoxyglucose-positron emission tomography imaging in a primate model of severe human malaria with cerebral involvementMunehiro Sugiyama, Eiji Ikeda, Satoru Kawai, et al.Oral and Maxillofacial Surgery|October 17, 2023
Mandibular reconstruction with TMJ prosthesis: management of osteomyelitis after orthognathic surgery (Case Report)Joao Victor Borges Leal, Luciano Mauro Del Santo, Omar Nasim Mohamed Nasim Khan Mahboob, et al.Primates; Journal of Primatology|February 15, 2013
Ranging and foraging of Himalayan grey langurs (Semnopithecus ajax) in Machiara National Park, PakistanRiaz Aziz Minhas, Usman Ali, Muhammad Siddique Awan, et al.The American Journal of Tropical Medicine and Hygiene|March 10, 2006
Enhancement of splenic glucose metabolism during acute malarial infection: correlation of findings of FDG-PET imaging with pathological changes in a primate model of severe human malariaSatoru Kawai, Eiji Ikeda, Munehiro Sugiyama, et al.Human Mutation|September 1, 2005
Novel sequence variants in the TMC1 gene in Pakistani families with autosomal recessive hearing impairmentRegie Lyn P Santos, Muhammad Wajid, Mohammad Nasim Khan, et al.BMJ Evidence-Based Medicine|November 12, 2020
Ten years later: a review of the US 2009 institute of medicine report on conflicts of interest and solutions for further reformTrevor Torgerson, Cole Wayant, Lisa Cosgrove, et al.Journal of Human Genetics|September 5, 2018
Novel missense and 3'-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairmentKhurram Liaqat, Ilene Chiu, Kwanghyuk Lee, et al.Investigative Ophthalmology & Visual Science|September 13, 2018
Confirmation of the Role of DHX38 in the Etiology of Early-Onset Retinitis PigmentosaZahid Latif, Imen Chakchouk, Isabelle Schrauwen, et al.Pageof 6