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1 . Academic Journal
The mitochondrial succinate dehydrogenase complex controls the STAT3-IL-10 pathway in inflammatory macrophages
저자
by
Gobelli, Dino
;
Serrano-Lorenzo, Pablo
;
Esteban-Amo, María J.
;
Serna, Julia
;
Pérez-García, M. Teresa
, et al.
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In
iScience
18 August 2023 26(8)
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7 . Academic Journal
Remarkable clinical improvement with oral nucleoside treatment in a patient with adult-onset TK2 deficiency: A case report
저자
by
Bermejo-Guerrero, Laura
;
Hernández-Voth, Ana
;
Serrano-Lorenzo, Pablo
;
Blázquez, Alberto
;
Martin-Jimenez, Paloma
, et al.
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In
Mitochondrion
May 2024 76
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7 . Academic Journal
Clinical and Genetic Analysis of Patients With TK2 Deficiency.
저자
by
Ceballos, Francisco
;
Serrano-Lorenzo, Pablo
;
Bermejo-Guerrero, Laura
;
Blázquez, Alberto
;
Quesada-Espinosa, Juan F.
, et al.
소스
Neurology: Genetics; Apr2024, Vol. 10 Issue 2, p1-13, 13p
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7 . Academic Journal
Development of a novel in vitro model to study the modulatory role of the respiratory complex I in macrophage effector functions.
저자
by
Serrano-Lorenzo, Pablo
;
Gobelli, Dino
;
Garrido-Moraga, Rocío
;
Esteban-Amo, María J.
;
López-López, José R.
, et al.
소스
PLoS ONE
. 9/19/203, Vol. 18 Issue 9, p1-15. 15p.
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7 . Academic Journal
Plasma LDH: A specific biomarker for lung affectation in COVID-19?
저자
by
Santos-Lozano, Alejandro
;
Cueto-Felgueroso, Cecilia
;
Pozo, Alba Fernández-del
;
de Miguel-Reyes, Montserrat
;
Serrano-Lorenzo, Pablo
, et al.
소스
In
Practical Laboratory Medicine
May 2021 25
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7 . Academic Journal
Serum GDF-15 Levels Accurately Differentiate Patients with Primary Mitochondrial Myopathy, Manifesting with Exercise Intolerance and Fatigue, from Patients with Chronic Fatigue Syndrome.
저자
by
Bermejo-Guerrero, Laura
;
de Fuenmayor-Fernández de la Hoz, Carlos Pablo
;
Guerrero-Molina, María Paz
;
Martín-Jiménez, Paloma
;
Blázquez, Alberto
, et al.
소스
Journal of Clinical Medicine
. Mar2023, Vol. 12 Issue 6, p2435. 9p.
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7 . Academic Journal
A Novel Mutation Associated with Neonatal Lethal Cardiomyopathy Leads to an Alternative Transcript Expression in the X-Linked Complex I NDUFB11 Gene.
저자
by
Amate-García, Guillermo
;
Ballesta-Martínez, María Juliana
;
Serrano-Lorenzo, Pablo
;
Garrido-Moraga, Rocío
;
González-Quintana, Adrián
, et al.
소스
International Journal of Molecular Sciences
. Jan2023, Vol. 24 Issue 2, p1743. 13p.
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7 . Academic Journal
Clinical, Biochemical, and Molecular Characterization of Two Families with Novel Mutations in the LDHA Gene (GSD XI).
저자
by
Serrano-Lorenzo, Pablo
;
Rabasa, María
;
Esteban, Jesús
;
Hidalgo Mayoral, Irene
;
Domínguez-González, Cristina
, et al.
소스
Genes
. Oct2022, Vol. 13 Issue 10, pN.PAG-N.PAG. 11p.
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7 . Academic Journal
A novel TRMT5 mutation causes a complex inherited neuropathy syndrome: The role of nerve pathology in defining a demyelinating neuropathy.
저자
by
Argente‐Escrig, Herminia
;
Vílchez, Juan J.
;
Frasquet, Marina
;
Muelas, Nuria
;
Azorín, Inmaculada
, et al.
소스
Neuropathology & Applied Neurobiology
. Aug2022, Vol. 48 Issue 5, p1-14. 14p.
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7 . Academic Journal
Identification of Potential Muscle Biomarkers in McArdle Disease: Insights from Muscle Proteome Analysis.
저자
by
García-Consuegra, Inés
;
Asensio-Peña, Sara
;
Garrido-Moraga, Rocío
;
Pinós, Tomàs
;
Domínguez-González, Cristina
, et al.
소스
International Journal of Molecular Sciences
. May2022, Vol. 23 Issue 9, p4650-4650. 18p.
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