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The British Journal of Dermatology|December 3, 2020
Risk factors for melanoma by anatomical site: an evaluation of aetiological heterogeneityR Laskar, A Ferreiro-Iglesias, D T Bishop, et al.Annals of Neurology|November 18, 2000
Multi-minicore disease--searching for boundaries: phenotype analysis of 38 casesA Ferreiro, B Estournet, D Chateau, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 24, 2014
Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolutionN Deconinck, P Richard, V Allamand, et al.Neurology|July 24, 2002
Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with coresH Jungbluth, C R Müller, B Halliger-Keller, et al.European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.Revista Espanola De Quimioterapia : Publicacion Oficial De La Sociedad Espanola De Quimioterapia|May 19, 2021
Clinical characteristics and outcomes of 1,331 patients with COVID-19: HM Spanish CohortP Cardinal-Fernández, E Garcia Cuesta, J Barberán, et al.The Pharmacogenomics Journal|April 22, 2015
Replication of PTPRC as genetic biomarker of response to TNF inhibitors in patients with rheumatoid arthritisA Ferreiro-Iglesias, A Montes, E Perez-Pampin, et al.Annals of Oncology : Official Journal of the European Society for Medical Oncology|June 12, 2019
Timing of HPV16-E6 antibody seroconversion before OPSCC: findings from the HPVC3 consortiumA R Kreimer, A Ferreiro-Iglesias, M Nygard, et al.Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Cross-ancestral GWAS identifies 29 novel variants across Head and Neck Cancer subsitesE Ebrahimi, A Sangphukieo, H A Park, et al.Pageof 8