Showing results (51-60 of 158) with videos related to
Sort By:
Pageof 16
BMC Endocrine Disorders|November 12, 2021
Causal variants in Maturity Onset Diabetes of the Young (MODY) - A systematic reviewIbrar Rafique, Asif Mir, Muhammad Arif Nadeem Saqib, et al.Annals of Neurology|January 26, 2012
Exome sequencing: dual role as a discovery and diagnostic toolChee-Seng Ku, David N Cooper, Constantin Polychronakos, et al.Annals of Human Genetics|June 12, 2012
Familial clustering strongly suggests that the phenotypic variation of the 8344 A>G lys mitochondrial tRNA mutation is encoded in cisKyriakos Kazakos, Kalliopi Kotsa, Maria Yavropoulou, et al.Plos One|August 20, 2014
Gene-specific function prediction for non-synonymous mutations in monogenic diabetes genesQuan Li, Xiaoming Liu, Richard A Gibbs, et al.Saudi Journal of Biological Sciences|October 10, 2022
Development of simple and effective PCR based assay to detect <i>PCCA</i> mutation (c.425G > A) among Saudi carriers and functional study of the homozygous <i>PCCA</i> mutationsAli Al-Asmari, Abdul Ali Peer-Zada, Abdulwahed AlDehaimi, et al.Pediatrics in Review|January 31, 2024
Congenital Adrenal HyperplasiaNicole R Fraga, Nare Minaeian, Mimi S KimEndocrinology, Diabetes & Metabolism Case Reports|October 22, 2014
One year remission of type 1 diabetes mellitus in a patient treated with sitagliptinMarcos M Lima-Martínez, Ernesto Guerra-Alcalá, Miguel Contreras, et al.Current Opinion in Endocrinology, Diabetes, and Obesity|October 6, 2012
Management of congenital adrenal hyperplasia in childhoodMimi S Kim, Anna Ryabets-Lienhard, Mitchell E GeffnerInternational Journal of Pediatric Otorhinolaryngology|June 28, 2026
Long-term quality of life outcomes after tympanostomy tube by surgical indicationMimi S Kim, Priya Sharma, Alex Irace, et al.Journal of Autoimmunity|February 27, 2017
The common, autoimmunity-predisposing 620Arg > Trp variant of PTPN22 modulates macrophage function and morphologyMeihang Li, Hugues Beauchemin, Natalija Popovic, et al.Pageof 16