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/vufind/Search/Results?lookfor=%22Pablo+Serrano-Lorenzo%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Pablo+Serrano-Lorenzo%22&type=Person&sort=year
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PubPharm (7)
1
A Novel Mutation Associated with Neonatal Lethal Cardiomyopathy Leads to an Alternative Transcript Expression in the X-Linked Complex I
in:
International Journal of Molecular Sciences
| 2023
von
Guillermo Amate-García
|
María Juliana Ballesta-Martínez
|
Pablo Serrano-Lorenzo
| +10
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2
Serum GDF-15 Levels Accurately Differentiate Patients with Primary Mitochondrial Myopathy, Manifesting with Exercise Intolerance and Fatigue, from Patients with Chronic Fatigue Syndrome
in:
Journal of Clinical Medicine
| 2023
von
Laura Bermejo-Guerrero
|
Carlos Pablo de Fuenmayor-Fernández de la Hoz
|
María Paz Guerrero-Molina
| +9
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3
Identification of Potential Muscle Biomarkers in McArdle Disease: Insights from Muscle Proteome Analysis
in:
International Journal of Molecular Sciences
| 2022
von
Inés García-Consuegra
|
Sara Asensio-Peña
|
Rocío Garrido-Moraga
| +10
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4
Plasma LDH: A specific biomarker for lung affectation in COVID-19?
in:
Practical Laboratory Medicine
| 2021
von
Pablo Serrano-Lorenzo
|
Olga N. Coya
|
Ana López-Jimenez
| +9
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5
Clinical, Histological, and Genetic Features of 25 Patients with Autosomal Dominant Progressive External Ophthalmoplegia (ad-PEO)/PEO-Plus Due to
in:
Journal of Clinical Medicine
| 2021
von
Laura Bermejo-Guerrero
|
Carlos Pablo de Fuenmayor-Fernández de la Hoz
|
Pablo Serrano-Lorenzo
| +10
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6
A Novel Missense Variant Associated with A Splicing Defect in A Myopathic Form of PGK1 Deficiency in The Spanish Population
in:
Genes
| 2019
von
Virginia Garcia-Solaesa
|
Pablo Serrano-Lorenzo
|
Maria Antonia Ramos-Arroyo
| +6
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7
Genotypic and phenotypic features of all Spanish patients with McArdle disease: a 2016 update
in:
BMC Genomics
| 2017
von
Alfredo Santalla
|
Gisela Nogales-Gadea
|
Alberto Blázquez Encinar
| +16
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1
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