Rebeca Martínez‐Hernández

Mutation update of spinal muscular atrophy in Spain: molecular characterization of 745 unrelated patients and identification of four novel mutations in the SMN1 gene

Laura Alías, Sara Bernal, Pablo Fuentes‐Prior et al. · Human Genetics · 2008 · 163 citations

Somatic Variant, Mendelian Disorder, Genetic Disorder +9

The Developmental Pattern of Myotubes in Spinal Muscular Atrophy Indicates Prenatal Delay of Muscle Maturation

Rebeca Martínez‐Hernández, Carolina Soler‐Botija, E. Also et al. · Journal of Neuropathology & Experimental Neurology · 2009 · 100 citations

Muscle Function, Genetics, Developmental Pattern +18

Synaptic defects in type I spinal muscular atrophy in human development

Rebeca Martínez‐Hernández, Sara Bernal, Eva Also‐Rallo et al. · The Journal of Pathology · 2012 · 89 citations

Genetics, Muscular Atrophy Patients, Muscular Atrophy +20

Pathogenic Th17 and Th22 cells are increased in patients with autoimmune thyroid disorders

Marlen Vitales‐Noyola, Ana M. Ramos‐Leví, Rebeca Martínez‐Hernández et al. · Endocrine · 2017 · 67 citations

Inflammation, Autoimmune Disease, T-regulatory Cell +12

Plastin 3 expression in discordant spinal muscular atrophy (SMA) siblings

Sara Bernal, Eva Also‐Rallo, Rebeca Martínez‐Hernández et al. · Neuromuscular Disorders · 2011 · 66 citations

Developmental Biology, Spinal Cord Injury, Skeletal Muscle +9