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Annals of Clinical and Translational Neurology
|
October 16, 2019
NOVEL intronic CAPN3 Roma mutation alters splicing causing RNA mediated decay
Fabiola Mavillard, Marcos Madruga-Garrido, Eloy Rivas, et al.
American Journal of Hematology
|
November 8, 2014
Bone marrow cellular cannibalism by medulloblastoma
Virginia Escamilla, Emilio Franco-Macías, Cristina Calderón-Cabrera, et al.
BMC Neurology
|
February 2, 2023
Lessons learned from a sporadic FUSopathy in a young man: a case report
Ernesto García-Roldán, Eloy Rivas-Infante, Manuel Medina-Rodríguez, et al.
Journal of Anatomy
|
May 24, 2021
Neuropeptides in the developing human hippocampus under hypoxic-ischemic conditions
Joaquín González Fuentes, Ricardo Insausti Serrano, Sandra Cebada Sánchez, et al.
Brain Imaging and Behavior
|
April 6, 2023
Study of the human hippocampal formation: a method for histological and magnetic resonance correlation in perinatal cases
Joaquín González Fuentes, Sandra Cebada-Sánchez, Maria Del Mar Arroyo-Jiménez, et al.
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology
|
May 18, 2025
IMMUNE SCENARIO IDENTIFICATION COMBINING MULTIPLEXED, QUANTITATIVE, AND ADVANCED IMAGING ANALYSIS COULD BE RELEVANT IN IMMUNOTHERAPY AGAINST GLIOBLASTOMA AND GRADE 4 ASTROCYTOMA
Miguel A Idoate, Mikel Ariz-Galilea, Ainhoa Urbiola-Casales, et al.
Pediatric Neurology
|
October 26, 2005
Macrophagic myofasciitis in childhood: a controversial entity
Eloy Rivas, Mercedes Gómez-Arnáiz, Jose R Ricoy, et al.
Cancers
|
November 25, 2020
Identification of VRK1 as a New Neuroblastoma Tumor Progression Marker Regulating Cell Proliferation
Ana Colmenero-Repiso, María A Gómez-Muñoz, Ismael Rodríguez-Prieto, et al.
Neuromuscular Disorders : NMD
|
June 17, 2023
Severe congenital X-linked myopathy with excessive autophagy secondary to an apparently synonymous but pathogenic novel variant
Patricia Blanco-Arias, Inmaculada Medina Martínez, Luisa Arrabal Fernández, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
July 3, 2024
A splice-altering homozygous variant in COX18 causes severe sensory-motor neuropathy with oculofacial apraxia
Fabiola Mavillard, Alejandra Guerra-Castellano, David Guerrero-Gómez, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 54) with videos related to
Sort By:
Page
of 6
Annals of Clinical and Translational Neurology
|
October 16, 2019
NOVEL intronic CAPN3 Roma mutation alters splicing causing RNA mediated decay
Fabiola Mavillard, Marcos Madruga-Garrido, Eloy Rivas, et al.
American Journal of Hematology
|
November 8, 2014
Bone marrow cellular cannibalism by medulloblastoma
Virginia Escamilla, Emilio Franco-Macías, Cristina Calderón-Cabrera, et al.
BMC Neurology
|
February 2, 2023
Lessons learned from a sporadic FUSopathy in a young man: a case report
Ernesto García-Roldán, Eloy Rivas-Infante, Manuel Medina-Rodríguez, et al.
Journal of Anatomy
|
May 24, 2021
Neuropeptides in the developing human hippocampus under hypoxic-ischemic conditions
Joaquín González Fuentes, Ricardo Insausti Serrano, Sandra Cebada Sánchez, et al.
Brain Imaging and Behavior
|
April 6, 2023
Study of the human hippocampal formation: a method for histological and magnetic resonance correlation in perinatal cases
Joaquín González Fuentes, Sandra Cebada-Sánchez, Maria Del Mar Arroyo-Jiménez, et al.
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology
|
May 18, 2025
IMMUNE SCENARIO IDENTIFICATION COMBINING MULTIPLEXED, QUANTITATIVE, AND ADVANCED IMAGING ANALYSIS COULD BE RELEVANT IN IMMUNOTHERAPY AGAINST GLIOBLASTOMA AND GRADE 4 ASTROCYTOMA
Miguel A Idoate, Mikel Ariz-Galilea, Ainhoa Urbiola-Casales, et al.
Pediatric Neurology
|
October 26, 2005
Macrophagic myofasciitis in childhood: a controversial entity
Eloy Rivas, Mercedes Gómez-Arnáiz, Jose R Ricoy, et al.
Cancers
|
November 25, 2020
Identification of VRK1 as a New Neuroblastoma Tumor Progression Marker Regulating Cell Proliferation
Ana Colmenero-Repiso, María A Gómez-Muñoz, Ismael Rodríguez-Prieto, et al.
Neuromuscular Disorders : NMD
|
June 17, 2023
Severe congenital X-linked myopathy with excessive autophagy secondary to an apparently synonymous but pathogenic novel variant
Patricia Blanco-Arias, Inmaculada Medina Martínez, Luisa Arrabal Fernández, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
July 3, 2024
A splice-altering homozygous variant in COX18 causes severe sensory-motor neuropathy with oculofacial apraxia
Fabiola Mavillard, Alejandra Guerra-Castellano, David Guerrero-Gómez, et al.
Page
of 6