Miguel Angel Martin (Miguel Ángel Martín, Miguel A Martin, Miguel A Martín, Miguel Angel Martín, Miguel Ángel Martin)

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 50

Top Venues

International journal of molecular sciences

Journal of clinical medicine

Genes

Neuroradiology

Hospital Universitario 12 de Octubre

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Hospital Universitario 12 de Octubre

Spain

Consultant, Principal Investigator :: Clinical Biochemistry, i+12 Research Institute

Publications

Marta García-López, Lydia Jiménez-Vicente, Raquel González-Jabardo, Helena Dorado, Irene Gomez-Manjon, Miguel Angel Martin, Carmen Ayuso, Joaquín Arenas, María Esther Gallardo
Creation of an Isogenic Human iPSC-Based RGC Model of Dominant Optic Atrophy Harboring the Pathogenic Variant c.1861C>T (p.Gln621Ter) in the OPA1 Gene. International journal of molecular sciences 25 (13) (2024)
Marta García-López, Lydia Jiménez-Vicente, Raquel González-Jabardo, Helena Dorado, Irene Gomez-Manjon, Miguel Angel Martin, Carmen Ayuso, Joaquín Arenas, María Esther Gallardo
Creation of an Isogenic Human iPSC-Based RGC Model of Dominant Optic Atrophy Harboring the Pathogenic Variant c.1861C>T (p.Gln621Ter) in the OPA1 Gene. International journal of molecular sciences 25 (13) (2024)
Francisco C Ceballos, Pablo Serrano-Lorenzo, Laura Bermejo-Guerrero, Alberto Blázquez, Juan F Quesada-Espinosa, Jorge Amigo, Pablo Minguez, Carmen Ayuso, Elena García-Arumí, Nuria Muelas, Teresa Jaijo, Andres Nascimento, Beatriz Galán-Rodriguez, Carmen Paradas, Joaquín Arenas, Angel Carracedo, Ramon Ramon, Miguel Angel Martin, Cristina Domínguez-González, null null
Clinical and Genetic Analysis of Patients With TK2 Deficiency. Neurology. Genetics 10 (2) (2024)
Francisco C Ceballos, Pablo Serrano-Lorenzo, Laura Bermejo-Guerrero, Alberto Blázquez, Juan F Quesada-Espinosa, Jorge Amigo, Pablo Minguez, Carmen Ayuso, Elena García-Arumí, Nuria Muelas, Teresa Jaijo, Andres Nascimento, Beatriz Galán-Rodriguez, Carmen Paradas, Joaquín Arenas, Angel Carracedo, Ramon Ramon, Miguel Angel Martin, Cristina Domínguez-González, null null
Clinical and Genetic Analysis of Patients With TK2 Deficiency. Neurology. Genetics 10 (2) (2024)
Marta García-López, Lydia Jiménez-Vicente, Raquel González-Jabardo, Helena Dorado, Irene Gomez-Manjon, Miguel Angel Martin, Carmen Ayuso, Joaquín Arenas, María Esther Gallardo
Creation of an Isogenic Human iPSC-Based RGC Model of Dominant Optic Atrophy Harboring the Pathogenic Variant c.1861C>T (p.Gln621Ter) in the OPA1 Gene. International journal of molecular sciences 25 (13) (2024)
María Paz Guerrero-Molina, Ángela Bernabeu-Sanz, Ana Ramos-González, Montserrat Morales-Conejo, Aitor Delmiro, Cristina Domínguez-González, Joaquín Arenas, Miguel Angel Martin, Jesús González de la Aleja
Magnetic resonance spectroscopy in MELAS syndrome: correlation with CSF and plasma metabolite levels and change after glutamine supplementation. Neuroradiology (2023)
Laura Bermejo-Guerrero, Carlos Pablo de Fuenmayor-Fernández de la Hoz, María Paz Guerrero-Molina, Paloma Martín-Jiménez, Alberto Blázquez-Encinar, Pablo Serrano-Lorenzo, David Lora-Pablos, Montserrat Morales-Conejo, Irene González-Martínez, Elena Ana López-Jiménez, Miguel Angel Martin, Cristina Domínguez-González
Serum GDF-15 Levels Accurately Differentiate Patients with Primary Mitochondrial Myopathy, Manifesting with Exercise Intolerance and Fatigue, from Patients with Chronic Fatigue Syndrome. Journal of clinical medicine 12 (6) (2023)
Laura Bermejo-Guerrero, Carlos Pablo de Fuenmayor-Fernández de la Hoz, María Paz Guerrero-Molina, Paloma Martín-Jiménez, Alberto Blázquez-Encinar, Pablo Serrano-Lorenzo, David Lora-Pablos, Montserrat Morales-Conejo, Irene González-Martínez, Elena Ana López-Jiménez, Miguel Angel Martin, Cristina Domínguez-González
Serum GDF-15 Levels Accurately Differentiate Patients with Primary Mitochondrial Myopathy, Manifesting with Exercise Intolerance and Fatigue, from Patients with Chronic Fatigue Syndrome. Journal of clinical medicine 12 (6) (2023)
Mariana I Muñoz-García, María Paz Guerrero-Molina, Carlos Pablo de Fuenmayor-Fernández de la Hoz, Laura Bermejo-Guerrero, Ana Arteche-López, Aurelio Hernández-Laín, Miguel Angel Martin, Cristina Domínguez-González
Delayed Diagnosis of Congenital Myasthenic Syndromes Erroneously Interpreted as Mitochondrial Myopathies. Journal of clinical medicine 12 (9) (2023)
Guillermo Amate-García, María Juliana Ballesta-Martínez, Pablo Serrano-Lorenzo, Rocío Garrido-Moraga, Adrián González-Quintana, Alberto Blázquez-Encinar, Juan C Rubio, Inés García-Consuegra, Joaquín Arenas, Cristina Ugalde, María Morán, Encarnación Guillén-Navarro, Miguel Angel Martin
A Novel Mutation Associated with Neonatal Lethal Cardiomyopathy Leads to an Alternative Transcript Expression in the X-Linked Complex I NDUFB11 Gene. International journal of molecular sciences 24 (2) (2023)
Miguel Fernández de la Torre, Carmen Fiuza-Luces, Sara Laine-Menéndez, Aitor Delmiro, Joaquín Arenas, Miguel Angel Martin, Alejandro Lucia, María Morán
Pathophysiology of Cerebellar Degeneration in Mitochondrial Disorders: Insights from the Harlequin Mouse. International journal of molecular sciences 24 (13) (2023)
Guillermo Amate-García, María Juliana Ballesta-Martínez, Pablo Serrano-Lorenzo, Rocío Garrido-Moraga, Adrián González-Quintana, Alberto Blázquez-Encinar, Juan C Rubio, Inés García-Consuegra, Joaquín Arenas, Cristina Ugalde, María Morán, Encarnación Guillén-Navarro, Miguel Angel Martin
A Novel Mutation Associated with Neonatal Lethal Cardiomyopathy Leads to an Alternative Transcript Expression in the X-Linked Complex I NDUFB11 Gene. International journal of molecular sciences 24 (2) (2023)
Mariana I Muñoz-García, María Paz Guerrero-Molina, Carlos Pablo de Fuenmayor-Fernández de la Hoz, Laura Bermejo-Guerrero, Ana Arteche-López, Aurelio Hernández-Laín, Miguel Angel Martin, Cristina Domínguez-González
Delayed Diagnosis of Congenital Myasthenic Syndromes Erroneously Interpreted as Mitochondrial Myopathies. Journal of clinical medicine 12 (9) (2023)
María Paz Guerrero-Molina, Ángela Bernabeu-Sanz, Ana Ramos-González, Montserrat Morales-Conejo, Aitor Delmiro, Cristina Domínguez-González, Joaquín Arenas, Miguel Angel Martin, Jesús González de la Aleja
Magnetic resonance spectroscopy in MELAS syndrome: correlation with CSF and plasma metabolite levels and change after glutamine supplementation. Neuroradiology 66 (3) (2023)
María Paz Guerrero-Molina, Ángela Bernabeu-Sanz, Ana Ramos-González, Montserrat Morales-Conejo, Aitor Delmiro, Cristina Domínguez-González, Joaquín Arenas, Miguel Angel Martin, Jesús González de la Aleja
Magnetic resonance spectroscopy in MELAS syndrome: correlation with CSF and plasma metabolite levels and change after glutamine supplementation. Neuroradiology 66 (3) (2023)
María Paz Guerrero-Molina, Ángela Bernabeu-Sanz, Ana Ramos-González, Montserrat Morales-Conejo, Aitor Delmiro, Cristina Domínguez-González, Joaquín Arenas, Miguel Angel Martin, Jesús González de la Aleja
Magnetic resonance spectroscopy in MELAS syndrome: correlation with CSF and plasma metabolite levels and change after glutamine supplementation. Neuroradiology 66 (3) (2023)
Guillermo Amate-García, María Juliana Ballesta-Martínez, Pablo Serrano-Lorenzo, Rocío Garrido-Moraga, Adrián González-Quintana, Alberto Blázquez-Encinar, Juan C Rubio, Inés García-Consuegra, Joaquín Arenas, Cristina Ugalde, María Morán, Encarnación Guillén-Navarro, Miguel Angel Martin
A Novel Mutation Associated with Neonatal Lethal Cardiomyopathy Leads to an Alternative Transcript Expression in the X-Linked Complex I NDUFB11 Gene. International journal of molecular sciences 24 (2) (2023)
Guillermo Amate-García, María Juliana Ballesta-Martínez, Pablo Serrano-Lorenzo, Rocío Garrido-Moraga, Adrián González-Quintana, Alberto Blázquez-Encinar, Juan C Rubio, Inés García-Consuegra, Joaquín Arenas, Cristina Ugalde, María Morán, Encarnación Guillén-Navarro, Miguel Angel Martin
A Novel Mutation Associated with Neonatal Lethal Cardiomyopathy Leads to an Alternative Transcript Expression in the X-Linked Complex I NDUFB11 Gene. International journal of molecular sciences 24 (2) (2023)
Adrián González-Quintana, Rocío Garrido-Moraga, Sara I Palencia-Pérez, Ángela Hernández-Martín, Jon Sánchez-Munárriz, Jose Miguel Lezana Rosales, Juan Francisco Quesada-Espinosa, Miguel Angel Martin, Ana Arteche-López
Integration of Phenotype Term Prioritization and Gene Expression Analysis Reveals a Novel Variant in the PERP Gene Associated with Autosomal Recessive Erythrokeratoderma. Genes 14 (7) (2023)
María Paz Guerrero-Molina, Ángela Bernabeu-Sanz, Ana Ramos-González, Montserrat Morales-Conejo, Aitor Delmiro, Cristina Domínguez-González, Joaquín Arenas, Miguel Angel Martin, Jesús González de la Aleja
Magnetic resonance spectroscopy in MELAS syndrome: correlation with CSF and plasma metabolite levels and change after glutamine supplementation. Neuroradiology 66 (3) (2023)
Guillermo Amate-García, María Juliana Ballesta-Martínez, Pablo Serrano-Lorenzo, Rocío Garrido-Moraga, Adrián González-Quintana, Alberto Blázquez-Encinar, Juan C Rubio, Inés García-Consuegra, Joaquín Arenas, Cristina Ugalde, María Morán, Encarnación Guillén-Navarro, Miguel Angel Martin
A Novel Mutation Associated with Neonatal Lethal Cardiomyopathy Leads to an Alternative Transcript Expression in the X-Linked Complex I NDUFB11 Gene. International journal of molecular sciences 24 (2) (2023)
Laura Bermejo-Guerrero, Carlos Pablo de Fuenmayor-Fernández de la Hoz, María Paz Guerrero-Molina, Paloma Martín-Jiménez, Alberto Blázquez-Encinar, Pablo Serrano-Lorenzo, David Lora-Pablos, Montserrat Morales-Conejo, Irene González-Martínez, Elena Ana López-Jiménez, Miguel Angel Martin, Cristina Domínguez-González
Serum GDF-15 Levels Accurately Differentiate Patients with Primary Mitochondrial Myopathy, Manifesting with Exercise Intolerance and Fatigue, from Patients with Chronic Fatigue Syndrome. Journal of clinical medicine 12 (6) (2023)
Nicoline Løkken, Karoline Lolk Revsbech, Laura Nørager Jacobsen, Andrea Martinuzzi, Miguel Angel Martin, Jordi Díaz-Manera, Cristina Dominguez-Gonzalez, Giovanni Brondani, Olimpia Musumeci, Francesca Granata, Cristina Stefan, Concepción Merino-Sanchez, Claudia Nuñez Peralta, Tahmina Khawajazada, Jorge Alonso-Pérez, Antonio Toscano, John Vissing
Muscle MRI in McArdle Disease: A European Multicenter Observational Study. Neurology (2022)
María Paz Guerrero-Molina, Montserrat Morales-Conejo, Aitor Delmiro, María Morán, Cristina Domínguez-González, Elena Arranz-Canales, Ana Ramos-González, Joaquín Arenas, Miguel Angel Martin, Jesús González de la Aleja
Elevated glutamate and decreased glutamine levels in the cerebrospinal fluid of patients with MELAS syndrome. Journal of neurology 269 (6) (2022)
Sara Laine-Menéndez, Miguel Fernández-de la Torre, Carmen Fiuza-Luces, Aitor Delmiro, Joaquín Arenas, Miguel Angel Martin, Patricia Boya, Alejandro Lucia, María Morán
Apoptosis-Inducing Factor Deficiency Induces Tissue-Specific Alterations in Autophagy: Insights from a Preclinical Model of Mitochondrial Disease and Exercise Training Effects. Antioxidants (Basel, Switzerland) 11 (3) (2022)
Pablo Serrano-Lorenzo, María Rabasa, Jesús Esteban, Irene Hidalgo Mayoral, Cristina Domínguez-González, Agustín Blanco-Echevarría, Rocío Garrido-Moraga, Alejandro Lucia, Alberto Blázquez-Encinar, Juan C Rubio, Carmen Palma Milla, Joaquín Arenas, Miguel Angel Martin
Clinical, Biochemical, and Molecular Characterization of Two Families with Novel Mutations in the LDHA Gene (GSD XI). Genes 13 (10) (2022)
Nuria Bujan, Constanza Morén, Francesc Josep García-García, Alberto Blázquez-Encinar, Clara Carnicer, Ana Belén Cortés, Cristina González, Ester López-Gallardo, Ester Lozano, Sonia Moliner, Laura Gort, Ester Tobías, Aitor Delmiro, Miguel Angel Martin, Miguel Ángel Fernández-Moreno, Eduardo Ruiz-Pesini, Elena Garcia-Arumí, Juan Carlos Rodríguez-Aguilera, Gloria Garrabou
Multicentric Standardization of Protocols for the Diagnosis of Human Mitochondrial Respiratory Chain Defects. Antioxidants (Basel, Switzerland) 11 (4) (2022)
Inés García-Consuegra, Sara Asensio, Rocío Garrido-Moraga, Tomàs Pinós, Cristina Domínguez-González, Alfredo Santalla, Gisela Nogales-Gadea, Pablo Serrano-Lorenzo, Antoni L Andreu, Joaquín Arenas, José Luis Zugaza, Alejandro Lucia, Miguel Angel Martin
Identification of Potential Muscle Biomarkers in McArdle Disease: Insights from Muscle Proteome Analysis. International journal of molecular sciences 23 (9) (2022)
María Paz Guerrero-Molina, Montserrat Morales-Conejo, Aitor Delmiro, María Morán, Cristina Domínguez-González, Elena Arranz-Canales, Ana Ramos-González, Joaquín Arenas, Miguel Angel Martin, Jesús González de la Aleja
High-dose oral glutamine supplementation reduces elevated glutamate levels in cerebrospinal fluid in patients with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome. European journal of neurology (2022)
Laura Bermejo-Guerrero, Carlos Pablo de Fuenmayor-Fernández de la Hoz, Pablo Serrano-Lorenzo, Alberto Blázquez-Encinar, Gerardo Gutiérrez-Gutiérrez, Laura Martínez-Vicente, Lucía Galán-Dávila, Jorge García-García, Joaquín Arenas, Nuria Muelas, Aurelio Hernández-Laín, Cristina Domínguez-González, Miguel Angel Martin
Clinical, Histological, and Genetic Features of 25 Patients with Autosomal Dominant Progressive External Ophthalmoplegia (ad-PEO)/PEO-Plus Due to TWNK Mutations. Journal of clinical medicine 11 (1) (2021)
Mónica Villarreal-Salazar, Astrid Brull, Gisela Nogales-Gadea, Antoni L Andreu, Miguel Angel Martin, Joaquín Arenas, Alfredo Santalla, Alejandro Lucia, John Vissing, Thomas O Krag, Tomàs Pinós
Preclinical Research in McArdle Disease: A Review of Research Models and Therapeutic Strategies. Genes 13 (1) (2021)
Marcello Bellusci, Abraham J Paredes-Fuentes, Eduardo Ruiz-Pesini, Beatriz Gómez, null null, Miguel Angel Martin, Julio Montoya, Rafael Artuch
The Genetic Landscape of Mitochondrial Diseases in Spain: A Nationwide Call. Genes 12 (10) (2021)
Daniel Toledo-Alfocea, Luísa Panadés-de Oliveira, Miguel Angel Martin, María I Álvarez-Mora, Aurelio Hernández-Lain, Cristina Domínguez-González
Pearls & Oy-sters: Hickam's Dictum in Genetic Myopathies: When a Proven Pathogenic Mutation Does Not Explain the Phenotype. Neurology 96 (21) (2021)
Sara Laine-Menéndez, Cristina Domínguez-González, Alberto Blázquez, Aitor Delmiro, Inés García-Consuegra, Miguel Fernández-de la Torre, Aurelio Hernández-Laín, Javier Sayas, Miguel Angel Martin, María Morán
Preferent Diaphragmatic Involvement in TK2 Deficiency: An Autopsy Case Study. International journal of molecular sciences 22 (11) (2021)
Ana Arteche-López, M I Álvarez-Mora, M T Sánchez Calvin, J M Lezana Rosales, C Palma Milla, M J Gómez Rodríguez, I Gomez Manjón, A Blázquez, A Juarez Rufián, P Ramos Gómez, O Sierra Tomillo, I Hidalgo Mayoral, Rubén Pérez de la Fuente, I J Posada Rodríguez, L I González Granado, Miguel Angel Martin, Juan Francisco Quesada-Espinosa, M Moreno-García
Biallelic variants in genes previously associated with dominant inheritance: CACNA1A, RET and SLC20A2. European journal of human genetics : EJHG 29 (10) (2021)
Ana Peñas, Miguel Fernández-De la Torre, Sara Laine-Menéndez, David Lora-Pablos, María Illescas, Alberto García-Bartolomé, Montserrat Morales-Conejo, Joaquín Arenas, Miguel Angel Martin, María Morán, Cristina Domínguez-González, Cristina Ugalde
Plasma Gelsolin Reinforces the Diagnostic Value of FGF-21 and GDF-15 for Mitochondrial Disorders. International journal of molecular sciences 22 (12) (2021)
Yanira Ruiz-Heredia, Alejandra Ortiz-Ruiz, Mehmet K Samur, Vanesa Garrido, Laura Rufian, Ricardo Sanchez, Pedro Aguilar-Garrido, Santiago Barrio, Miguel Angel Martin, Niccolo' Bolli, Yu-Tzu Tai, Raphaël Szalat, Mariateresa Fulciniti, Nikhil Munshi, Joaquin Martinez Lopez, María Linares, Miguel Gallardo
Pathogenetic and Prognostic Implications of Increased Mitochondrial Content in Multiple Myeloma. Cancers 13 (13) (2021)
Aitana Almodóvar-Payá, Mónica Villarreal-Salazar, Noemí de Luna, Gisela Nogales-Gadea, Alberto Real-Martínez, Antoni L Andreu, Miguel Angel Martin, Joaquin Arenas, Alejandro Lucia, John Vissing, Thomas O Krag, Tomàs Pinós
Preclinical Research in Glycogen Storage Diseases: A Comprehensive Review of Current Animal Models. International journal of molecular sciences 21 (24) (2020)
Alberto García-Bartolomé, Ana Peñas, María Illescas, Verónica Bermejo, Sandra López-Calcerrada, Rafael Pérez-Pérez, Lorena Marín-Buera, Cristina Domínguez-González, Joaquín Arenas, Miguel Angel Martin, Cristina Ugalde
Altered Expression Ratio of Actin-Binding Gelsolin Isoforms Is a Novel Hallmark of Mitochondrial OXPHOS Dysfunction. Cells 9 (9) (2020)
Claudia Rodríguez-López, Luis M García-Cárdaba, Alberto Blázquez, Pablo Serrano-Lorenzo, Gerardo Gutiérrez-Gutiérrez, Beatriz San Millán-Tejado, Nuria Muelas, Aurelio Hernández-Laín, Juan J Vílchez, Eduardo Gutiérrez-Rivas, Joaquín Arenas, Miguel Angel Martin, Cristina Domínguez-González
Clinical, pathological and genetic spectrum in 89 cases of mitochondrial progressive external ophthalmoplegia. Journal of medical genetics 57 (9) (2020)
Adrián González-Quintana, Inés García-Consuegra, Amaya Belanger-Quintana, Pablo Serrano-Lorenzo, Alejandro Lucia, Alberto Blázquez, Jorge Docampo, Cristina Ugalde, María Morán, Joaquín Arenas, Miguel Angel Martin
Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report. Genes 11 (8) (2020)
Teresa Galera-Monge, Francisco Zurita-Díaz, Isaac Canals, Marita Grønning Hansen, Laura Rufián-Vázquez, Johannes K Ehinger, Eskil Elmér, Miguel Angel Martin, Rafael Garesse, Henrik Ahlenius, María Esther Gallardo
Mitochondrial Dysfunction and Calcium Dysregulation in Leigh Syndrome Induced Pluripotent Stem Cell Derived Neurons. International journal of molecular sciences 21 (9) (2020)
Guillermo Tarrasó, Alberto Real-Martinez, Marta Parés, Lídia Romero-Cortadellas, Laura Puigros, Laura Moya-Borrego, Noemí de Luna, Astrid Brull, Miguel Angel Martin, Joaquin Arenas, Alejandro Lucia, Antoni L Andreu, Jordi Barquinero, John Vissing, Thomas O Krag, Tomàs Pinós
Absence of p.R50X Pygm read-through in McArdle disease cellular models. Disease models & mechanisms 13 (1) (2020)
Alberto Real-Martinez, Astrid Brull, Jordi Huerta, Guillermo Tarrasó, Alejandro Lucia, Miguel Angel Martin, Joaquin Arenas, Antoni L Andreu, Gisela Nogales-Gadea, John Vissing, Thomas O Krag, Noemi de Luna, Tomàs Pinós
Low survival rate and muscle fiber-dependent aging effects in the McArdle disease mouse model. Scientific reports 9 (1) (2019)
Irene Bravo-Alonso, Rosa Navarrete, Ana Isabel Vega, Pedro Ruíz-Sala, María Teresa García Silva, Elena Martín-Hernández, Pilar Quijada-Fraile, Amaya Belanger-Quintana, Sinziana Stanescu, María Bueno, Isidro Vitoria, Laura Toledo, Maria-Luz Couce, Inmaculada García-Jiménez, Ricardo Ramos, Miguel Angel Martin, Lourdes R Desviat, Magdalena Ugarte, Celia Pérez-Cerdá, Begoña Merinero, Belén Pérez, Pilar Rodríguez-Pombo
Genes and Variants Underlying Human Congenital Lactic Acidosis-From Genetics to Personalized Treatment. Journal of clinical medicine 8 (11) (2019)
Virginia Garcia-Solaesa, Pablo Serrano-Lorenzo, Maria Antonia Ramos-Arroyo, Alberto Blázquez, Inmaculada Pagola-Lorz, Mercè Artigas-López, Joaquín Arenas, Miguel Angel Martin, Ivonne Jericó-Pascual
A Novel Missense Variant Associated with A Splicing Defect in A Myopathic Form of PGK1 Deficiency in The Spanish Population. Genes 10 (10) (2019)
Rachid Boutoual, Salvador Meseguer, Magda Villarroya, Elena Martín-Hernández, Mohammed Errami, Miguel Angel Martin, Marta Casado, M-Eugenia Armengod
Defects in the mitochondrial-tRNA modification enzymes MTO1 and GTPBP3 promote different metabolic reprogramming through a HIF-PPARγ-UCP2-AMPK axis. Scientific reports 8 (1) (2018)
Carmen Fiuza-Luces, Alejandro Santos-Lozano, Francisco Llavero, Rocío Campo, Gisela Nogales-Gadea, Jorge Díez-Bermejo, Carlos Baladrón, África González-Murillo, Joaquín Arenas, Miguel Angel Martin, Antoni L Andreu, Tomàs Pinós, Beatriz G Gálvez, Juan Antonio López, Jesús Vázquez, José L Zugaza, Alejandro Lucia
Muscle molecular adaptations to endurance exercise training are conditioned by glycogen availability: a proteomics-based analysis in the McArdle mouse model. The Journal of physiology 596 (6) (2018)
Caterina Garone, Robert W Taylor, Andrés Nascimento, Joanna Poulton, Carl Fratter, Cristina Domínguez-González, Julie C Evans, Mariana Loos, Pirjo Isohanni, Anu Suomalainen, Dipak Ram, M Imelda Hughes, Robert McFarland, Emanuele Barca, Carlos Lopez-Gomez, Sandeep Jayawant, Neil D Thomas, Adnan Y Manzur, Karin Kleinsteuber, Miguel Angel Martin, Timothy Kerr, Grainne S Gorman, Ewen W Sommerville, Patrick F Chinnery, Monika Hofer, Christoph Karch, Jeffrey Ralph, Yolanda Cámara, Marcos Madruga-Garrido, Jana Domínguez-Carral, Carlos Ortez, Sonia Emperador, Julio Montoya, Anupam Chakrapani, Joshua F Kriger, Robert Schoenaker, Bruce Levin, John L P Thompson, Yuelin Long, Shamima Rahman, Maria Alice Donati, Salvatore DiMauro, Michio Hirano
Retrospective natural history of thymidine kinase 2 deficiency. Journal of medical genetics 55 (8) (2018)
Ines Garcia-Consuegra, Alberto Blázquez-Encinar, Juan Carlos Rubio, Joaquín Arenas, Alfonsina Ballester-Lopez, Adrián González-Quintana, Antoni L Andreu, Tomàs Pinós, Jaume Coll-Cantí, Alejandro Lucia, Gisela Nogales-Gadea, Miguel Angel Martin
Taking advantage of an old concept, "illegitimate transcription", for a proposed novel method of genetic diagnosis of McArdle disease. Genetics in medicine : official journal of the American College of Medical Genetics 18 (11) (2016)

Miguel Angel Martin.css-eqlu8i{font-size:small;padding-left:4px;} (Miguel Ángel Martín, Miguel A Martin, Miguel A Martín, Miguel Angel Martín, Miguel Ángel Martin)

Publication Activity (10 Years)

Top Topics

Top Venues

Miguel Angel Martin (Miguel Ángel Martín, Miguel A Martin, Miguel A Martín, Miguel Angel Martín, Miguel Ángel Martin)