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Eloy Rivas

Showing results (1-10 of 54) with videos related to

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Hematology, Transfusion and Cell Therapy|December 20, 2021
Conus medullaris syndrome caused by intravascular large B cell lymphomaMarta González-Pombo, Marta Ordóñez-Carmona, Eloy Rivas Infante
Clinical Genetics|April 5, 2021
Novel ANO5 intronic Roma variant alters splicing causing muscular dystrophyFabiola Mavillard, Emilia Servián-Morilla, Eloy Rivas, et al.
Journal of Clinical Neuromuscular Disease|December 3, 2025
A Distinctive MRI Pattern Resembling Type VI Collagen Myopathy in Novel VWA1-Related Distal Hereditary Motor Neuronopathy With Myopathic Features in a Patient From SpainAldo F Costa, Teresa Gómez Caravaca, Sandra Rodríguez Navas, et al.
Medicina Clinica|July 7, 2014
[Erdheim-Chester disease]Francisco Javier García-Gómez, Irene Acevedo-Báñez, Eloy Rivas-Infante, et al.
Neurology|January 11, 2013
TK2 mutation presenting as indolent myopathyCarmen Paradas, Purificacion Gutiérrez Ríos, Eloy Rivas, et al.
Journal of Biomedical Optics|June 28, 2013
Neuromuscular disease classification systemAurora Sáez, Begoña Acha, Adoración Montero-Sánchez, et al.
Pediatric Hematology and Oncology|November 13, 2012
Primary cerebral radiotherapy-induced rhabdomyosarcoma: treatment with intraoperative carmustine implantsMónica Rivero-Garvía, Javier Márquez-Rivas, Eloy Rivas, et al.
Archives of Neurology|July 21, 2004
A new rare mutation (691delCC/insAAA) in exon 17 of the PYGM gene causing McArdle diseaseBeatriz Quintans, Amalia Sanchez-Andrade, Susana Teijeira, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|May 7, 2005
Miliary brain metastases presenting as rapidly progressive dementiaEloy Rivas, Joaquin Sanchez-Herrero, Miguel Alonso, et al.
Journal of the Neurological Sciences|October 22, 2008
Phenotypic variability in a Spanish family with a Caveolin-3 mutationPaloma González-Pérez, Pía Gallano, Lidia González-Quereda, et al.
Pageof 6

Showing results (1-10 of 54) with videos related to

Sort By:
Pageof 6
Hematology, Transfusion and Cell Therapy|December 20, 2021
Conus medullaris syndrome caused by intravascular large B cell lymphomaMarta González-Pombo, Marta Ordóñez-Carmona, Eloy Rivas Infante
Clinical Genetics|April 5, 2021
Novel ANO5 intronic Roma variant alters splicing causing muscular dystrophyFabiola Mavillard, Emilia Servián-Morilla, Eloy Rivas, et al.
Journal of Clinical Neuromuscular Disease|December 3, 2025
A Distinctive MRI Pattern Resembling Type VI Collagen Myopathy in Novel VWA1-Related Distal Hereditary Motor Neuronopathy With Myopathic Features in a Patient From SpainAldo F Costa, Teresa Gómez Caravaca, Sandra Rodríguez Navas, et al.
Medicina Clinica|July 7, 2014
[Erdheim-Chester disease]Francisco Javier García-Gómez, Irene Acevedo-Báñez, Eloy Rivas-Infante, et al.
Neurology|January 11, 2013
TK2 mutation presenting as indolent myopathyCarmen Paradas, Purificacion Gutiérrez Ríos, Eloy Rivas, et al.
Journal of Biomedical Optics|June 28, 2013
Neuromuscular disease classification systemAurora Sáez, Begoña Acha, Adoración Montero-Sánchez, et al.
Pediatric Hematology and Oncology|November 13, 2012
Primary cerebral radiotherapy-induced rhabdomyosarcoma: treatment with intraoperative carmustine implantsMónica Rivero-Garvía, Javier Márquez-Rivas, Eloy Rivas, et al.
Archives of Neurology|July 21, 2004
A new rare mutation (691delCC/insAAA) in exon 17 of the PYGM gene causing McArdle diseaseBeatriz Quintans, Amalia Sanchez-Andrade, Susana Teijeira, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|May 7, 2005
Miliary brain metastases presenting as rapidly progressive dementiaEloy Rivas, Joaquin Sanchez-Herrero, Miguel Alonso, et al.
Journal of the Neurological Sciences|October 22, 2008
Phenotypic variability in a Spanish family with a Caveolin-3 mutationPaloma González-Pérez, Pía Gallano, Lidia González-Quereda, et al.
Pageof 6