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Scientific Reports|April 6, 2018
Differential expression of microRNAs and other small RNAs in muscle tissue of patients with ALS and healthy age-matched controlsAnja Kovanda, Lea Leonardis, Janez Zidar, et al.Frontiers in Molecular Neuroscience|April 20, 2018
Differential Expression of Several miRNAs and the Host Genes <i>AATK</i> and <i>DNM2</i> in Leukocytes of Sporadic ALS PatientsKatarina Vrabec, Emanuela Boštjančič, Blaž Koritnik, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 7, 2020
Improvements in the multidisciplinary care are beneficial for survival in amyotrophic lateral sclerosis (ALS): experience from a tertiary ALS centerPolona Klavžar, Blaž Koritnik, Lea Leonardis, et al.Neurobiology of Aging|January 15, 2015
Genetic analysis of amyotrophic lateral sclerosis in the Slovenian populationKatarina Vrabec, Blaž Koritnik, Lea Leonardis, et al.Human Molecular Genetics|September 13, 2005
Complete loss-of-function of the heart/muscle-specific adenine nucleotide translocator is associated with mitochondrial myopathy and cardiomyopathyLuigi Palmieri, Simona Alberio, Isabella Pisano, et al.Brain and Language|September 16, 2016
Beyond aphasia: Altered EEG connectivity in Broca's patients during working memory taskVeronika Rutar Gorišek, Vlasta Zupanc Isoski, Aleš Belič, et al.Journal of Medical Genetics|January 13, 2021
Chromosome 10q-linked FSHD identifies <i>DUX4</i> as principal disease geneRichard J L F Lemmers, Patrick J van der Vliet, Ana Blatnik, et al.American Journal of Human Genetics|January 4, 2011
Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type IChristian Guelly, Peng-Peng Zhu, Lea Leonardis, et al.Nature Genetics|March 31, 2026
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosisPaul J Hop, Maarten Kooyman, Brendan J Kenna, et al.Nature Genetics|July 26, 2016
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosisWouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, et al.Pageof 4