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Liver International : Official Journal of the International Association for the Study of the Liver|January 27, 2021
Clinicopathologic and MRI features of combined hepatocellular-cholangiocarcinoma in patients with or without cirrhosisJongjin Yoon, Jeong A Hwang, Sunyoung Lee, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 10, 2012
Subcortical white matter hyperintensities within the cholinergic pathways of Parkinson's disease patients according to cognitive statusJaeseung Shin, Sungeun Choi, Ji E Lee, et al.Journal of Molecular Neuroscience : MN|October 4, 2024
Clinical and Molecular Profiles of a Cohort of Egyptian Patients with Collagen VI-Related DystrophyWessam E Sharaf-Eldin, Karima Rafat, Mahmoud Y Issa, et al.American Journal of Medical Genetics. Part A|March 23, 2016
Extending the mutation spectrum for Galloway-Mowat syndrome to include homozygous missense mutations in the WDR73 geneRasim O Rosti, Esra Dikoglu, Maha S Zaki, et al.Annals of Neurology|May 1, 2016
PYCR2 Mutations cause a lethal syndrome of microcephaly and failure to thriveMaha S Zaki, Gifty Bhat, Tipu Sultan, et al.NPJ Genomic Medicine|January 29, 2022
Oligonucleotide correction of an intronic TIMMDC1 variant in cells of patients with severe neurodegenerative disorderRaman Kumar, Mark A Corbett, Nicholas J C Smith, et al.Journal of Medical Genetics|May 23, 2020
Bi-allelic TTC5 variants cause delayed developmental milestones and intellectual disabilityArisha Rasheed, Evren Gumus, Maha Zaki, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 13, 2009
A comparison of gray and white matter density in patients with Parkinson's disease dementia and dementia with Lewy bodies using voxel-based morphometryJi E Lee, Bosuk Park, Sook K Song, et al.The Laryngoscope|September 13, 2014
The prevalence of hearing loss in South Korea: data from a population-based studyHyung J Jun, Soon Y Hwang, Soo H Lee, et al.BMC Medical Genomics|May 15, 2020
Molecular diagnosis in recessive pediatric neurogenetic disease can help reduce disease recurrence in familiesMahmoud Y Issa, Zinayida Chechlacz, Valentina Stanley, et al.Pageof 34