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Hematology, Transfusion and Cell Therapy
|
December 20, 2021
Conus medullaris syndrome caused by intravascular large B cell lymphoma
Marta González-Pombo, Marta Ordóñez-Carmona, Eloy Rivas Infante
Clinical Genetics
|
April 5, 2021
Novel ANO5 intronic Roma variant alters splicing causing muscular dystrophy
Fabiola 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 Spain
Aldo 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 myopathy
Carmen Paradas, Purificacion Gutiérrez Ríos, Eloy Rivas, et al.
Journal of Biomedical Optics
|
June 28, 2013
Neuromuscular disease classification system
Aurora Sáez, Begoña Acha, Adoración Montero-Sánchez, et al.
Pediatric Hematology and Oncology
|
November 13, 2012
Primary cerebral radiotherapy-induced rhabdomyosarcoma: treatment with intraoperative carmustine implants
Mónica 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 disease
Beatriz 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 dementia
Eloy 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 mutation
Paloma González-Pérez, Pía Gallano, Lidia González-Quereda, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 54) with videos related to
Sort By:
Page
of 6
Hematology, Transfusion and Cell Therapy
|
December 20, 2021
Conus medullaris syndrome caused by intravascular large B cell lymphoma
Marta González-Pombo, Marta Ordóñez-Carmona, Eloy Rivas Infante
Clinical Genetics
|
April 5, 2021
Novel ANO5 intronic Roma variant alters splicing causing muscular dystrophy
Fabiola 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 Spain
Aldo 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 myopathy
Carmen Paradas, Purificacion Gutiérrez Ríos, Eloy Rivas, et al.
Journal of Biomedical Optics
|
June 28, 2013
Neuromuscular disease classification system
Aurora Sáez, Begoña Acha, Adoración Montero-Sánchez, et al.
Pediatric Hematology and Oncology
|
November 13, 2012
Primary cerebral radiotherapy-induced rhabdomyosarcoma: treatment with intraoperative carmustine implants
Mónica 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 disease
Beatriz 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 dementia
Eloy 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 mutation
Paloma González-Pérez, Pía Gallano, Lidia González-Quereda, et al.
Page
of 6