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Neurology|December 12, 2001
Inflammation in dysferlin myopathy: immunohistochemical characterization of 13 patientsE Gallardo, R Rojas-García, N de Luna, et al.Nucleic Acids Research|June 14, 2021
The ribosome assembly factor Nop53 has a structural role in the formation of nuclear pre-60S intermediates, affecting late maturation eventsFelipe F M Bagatelli, Francisca N de Luna Vitorino, Julia P C da Cunha, et al.Neurology|December 25, 2003
Chronic neuropathy with IgM anti-ganglioside antibodies: lack of long term response to rituximabR Rojas-García, E Gallardo, I de Andrés, et al.Cell Reports|April 24, 2026
Comprehensive mass spectrometry screening-derived atlas of HDAC inhibitors reveals histone-specific acetylation changesRashmi Karki, Francisca N De Luna Vitorino, Richard M Searfoss, et al.Science Signaling|February 24, 2026
Acetate enhances long-term memory in female mice by sex-, context-, and brain region-specific epigenetic and transcriptional remodelingErica M Periandri, Kala M Dodson, Francisca N de Luna Vitorino, et al.European Journal of Neurology|June 11, 2011
Abnormal expression of dysferlin in skeletal muscle and monocytes supports primary dysferlinopathy in patients with one mutated alleleM Meznaric, L Gonzalez-Quereda, E Gallardo, et al.Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|November 11, 2011
Identification of novel GH-regulated genes in C2C12 cellsE Resmini, B Morte, E Sorianello, et al.Neurology|February 9, 2007
Symptomatic dysferlin gene mutation carriers: characterization of two casesI Illa, N De Luna, R Domínguez-Perles, et al.Neuromuscular Disorders : NMD|December 17, 2008
A new phenotype of dysferlinopathy with congenital onsetC Paradas, L González-Quereda, N De Luna, et al.Medicina Clinica|July 7, 2001
[Anti-GQ1b antibodies: usefulness of its detection for the diagnosis of Miller-Fisher syndrome]R Rojas-García, E Gallardo, C Serrano-Munuera, et al.Pageof 3