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Frontiers in Neurology|April 25, 2022
Seven Years of Selective Genetic Screening Program and Follow-Up of Asymptomatic Carriers With Hereditary Transthyretin Amyloidosis in BulgariaTeodora Chamova, Mariana Gospodinova, Ognian Asenov, et al.The International Journal of Artificial Organs|July 15, 2017
Hypomagnesemia and cause-specific mortality in hemodialysis patients: 5-year follow-up analysisGjulsen N Selim, Goce Spasovski, Liljana Tozija, et al.Clinical Kidney Journal|February 24, 2021
Uric acid and left ventricular hypertrophy: another relationship in hemodialysis patientsGjulsen Selim, Olivera Stojceva-Taneva, Liljana Tozija, et al.Wiener Medizinische Wochenschrift (1946)|October 12, 2012
Onychomycosis: modern diagnostic and treatment approachesGeorgi Tchernev, Plamen Kolev Penev, Pietro Nenoff, et al.Journal of Human Evolution|September 7, 2017
Evidence of Neanderthals in the Balkans: The infant radius from Kozarnika Cave (Bulgaria)Anne-Marie Tillier, Nikolay Sirakov, Aleta Guadelli, et al.Neuromuscular Disorders : NMD|May 31, 2021
MYH7-related disorders in two Bulgarian families: Novel variants in the same region associated with different clinical manifestation and disease penetranceSlavena Atemin, Tihomir Todorov, Ales Maver, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 29, 2008
Assessment of urea removal in haemodialysis and the impact of the European Best Practice GuidelinesCécile Couchoud, Kitty J Jager, Charlie Tomson, et al.Genes|September 28, 2024
Phenotypic Variability of LGMD 2C/R5 in a Genetically Homogenous Group of Bulgarian Muslim RomaAni Taneva, David Gresham, Velina Guergueltcheva, et al.Wiener Medizinische Wochenschrift (1946)|January 16, 2013
Atypical fibroxanthoma-a diagnosis of exclusion!Georgi Tchernev, Michael Tronnier, Julian Ananiev, et al.Neuromuscular Disorders : NMD|June 25, 2018
Limb girdle muscular dystrophy 2G in a religious minority of Bulgarian Muslims homozygous for the c.75G>A, p.Trp25X mutationTeodora Chamova, Stoyan Bichev, Tihomir Todorov, et al.Pageof 28